Toward Self‐Supported Bifunctional Air Electrodes for Flexible Solid‐State Zn–Air Batteries

The demand for flexibility and rechargeability in tandem with high energy density, reliability, and safety in energy‐storage devices to power wearable electronics has translated to significant advances in flexible solid‐state Zn–air batteries (FSZABs) technology. FSZABs using self‐supported bifunctional air electrodes are currently one of the most attractive alternatives to Li‐ion battery technology for next‐generation wearable electronics. Unlike the conventional powder‐based air electrodes, self‐supported bifunctional air electrodes offer higher electron‐transfer rate, larger specific surface area (and catalyst–reactant–product interfacial contact area), mechanical flexibility, and better operational robustness. To realize their potential nonetheless, self‐supported bifunctional air electrodes should have high and stable bifunctional catalytic activity, low cost, and environmental compatibility. This review first summarizes the three typical configurations and working principles of FSZABs. Then, significant development of self‐supported bifunctional air electrodes for FSZABs and efficient synthesis strategies are emphasized. The review concludes by providing perspectives on how to further improve the electrochemical performance of FSZABs and their suitability for next‐generation wearable electronic devices.

In this review, we focus on the self-supported bifunctional air electrodes for FSZABs (Figure 1).We first discuss the battery configuration and working principles.Then, we discuss the ORR and OER mechanisms and their performance evaluation criteria.Next, we summarize the advances toward powder catalysts and the drawbacks of powder catalysts in rechargeable ZABs.We mainly highlight a detailed overview summary of self-supported bifunctional air electrodes in FSZABs, categorizing them into metal-free carbon materials, transition metals/conductive substrates, transition metal compounds/conductive substrates, and other air electrodes.Before concluding this review with our perspectives on the FSZABs' development for wearable electronic devices, we also discuss different synthesis strategies for self-supported air electrodes in detail.

Battery Configuration
Besides high energy efficiency and outstanding mechanical properties under various formation states, battery configuration also occupies a vital position in determining the electrocatalytic performance of these FSZABs and wearable electronic devices. [9]ere, we focus on three types of FSZABs configurations, i.e., sandwich, cable, and coplanar.Sandwich-type ZABs are the most popular configuration for FSZABs.They comprise a Zn anode, solid-state electrolyte membrane, and air cathode stacked side by side (Figure 2a).The sandwich-like structure endows excellent bending, twisting, and stretching proprieties, which well suits small wearable applications. [10]Compared with sandwich-type ZABs, the cable-type ZABs exhibit more outstanding mechanical properties and higher volumetric energy density since their appearance in 2014. [11]For cable-type ZABs, the Zn anode comprises a membrane-wrapped electrolyte encapsulated with a breathable heat shrink tube (Figure 2b).Cable-type ZABs can be promising upcoming wearable and compact energy-storage devices because they can be part of integrated fashion design for powering wearable electronics. [11,12]Finally, coplanar-type ZABs, which have been recently explored, is also compatible for wearable electronic devices application.The air cathode and ZN anode are purposely arranged in a plane and on the same side as the electrode for coplanar-type ZABs (Figure 2c).Such a configuration can provide robust flexibility and coplanar integrability, preventing the solid electrolyte film to be detached from the electrode when it deforms under repeating bending. [13]

Working Principles
A typical ZAB comprises an air cathode, Zn anode, and conductive electrolyte.Its working principles can be divided into discharging process and charging process (Equation (1)).During the discharging process, the anode Zn is oxidized (Equation (2)) and finally decomposes into ZnO (Equation (3)), while the oxygen in cathode is reduced to OH -ions (Equation (4)).Moreover, ZnO can be reduced to Zn metal via the reversible reaction in the Zn anode.And OH À ions can be oxidized to O 2 in the air cathode during the charging process. [14]erall reaction : 2Zn þ O 2 ↔ 2ZnO ðE eq ¼ 1:65 V vs SHEÞ (1) Zn anode : Zn þ 4OH À ↔ ZnðOHÞ 2À 4 þ 2e À (2) Figure 1.Summary of powder-based air electrodes, self-supported air electrodes, and synthesis strategies of self-supported air electrodes for ZABs.
Besides the aforementioned electrochemical reactions, the theoretical and working voltages are the other critical factors affecting the performance of ZABs.1a,15] However, a high potential gap, low round-trip energy efficiency, and poor long-term durability may significantly constrain the overall performance of the rechargeable ZABs.Besides that, the mechanical properties of ZABs are also essential for the outstanding electrochemical performances of wearable and power devices. [16]Therefore, many researchers have devoted their studies to air cathodes, Zn anodes, and electrolytes, improving the ZAB's rechargeable performance and mechanical flexibility properties.
5b,17] Several attempts have been performed recently to overcome these setbacks.For example, Liu and co-workers introduced anode additives (metal elements and relative oxides), modified Zn morphology, and electrodeposited Zn particles on flexible carbon cloth. [18]Another challenge, such as the evaporation and leakage of the liquid electrolytes when using KOH alkaline solution (6 M), can degrade the lifetime of rechargeable ZABs, and packaging limitation of liquid electrolytes also causes the excessive weight of batteries, which could not meet the requirements of flexible devices. [19]Hence, other types of alkaline gel electrolytes have been considered, which could conduct ions, separate the electrodes, and support the flexible structures.For example, poly(acrylic acid) (PAA), poly(vinyl alcohol) (PVA), poly(ethylene oxide) (PEO), and polyacrylamide (PAM) are currently some of the promising solid electrolytes for FSZABs, given their high conductivity, suitable water retention, and desired mechanical properties. [20]n the other hand, air cathode preparation methods can be time-consuming, complicated, and ineffective. [21]This is because the traditional air cathode comprises powder catalysts, conductive agents, polymer binders, and conductive substrates for forming a conductive network.Conductive agents (acetylene or super P carbon black) addition to the battery generally leads to increased weight and enhanced corrosion during the charging, which can weaken its performance. [22]Similarly, when the polymer binders (Nafion and PTFE) are added to the battery, the interfacial resistance typically increases due to the blockage of the active catalytic sites, which reduces the battery's lifetime. [23]iven the aforementioned explanations, the subsequent discussions will focus onto the self-supported air electrodes for the FSZABs.The self-supported air electrodes should possess several advantages as follows: 1) their use avoids the need to add more conductive agents and polymer binders, giving better scalability; 2) these electrodes possess larger interfacial contact area between the catalysts and substrates with high charge transfer rate, excellent flexibility, and stability; and finally 3) these electrodes allow better catalysts dispersion and thus, more catalytically active sites.Usually, we construct a self-supported air electrode by directly growing catalysts on conductive substrates with controlled nanostructure and morphology to meet the requirements of the latest intelligent wearable technology and wireless communication applications. [24]he substrates for FSZABs should possess excellent flexibility, air permeability, high electronic conductivity, and robust mechanical performance when undergoing repetitive shape deformation.In general, metal and carbon-based substrates are usually chosen as the conductive substrates for FSZABs.Metal-based substrates have the advantages of high conductivity, mechanical strength, and stability, which possess satisfactory mechanical properties when FSZABs are subjected to complex and repeated deformation.Metal-based substrates mainly include metal foils, metal meshes, and metal foams. [25]First, the solid structure of metal foils will hinder the continuous supply of oxygen and reduce the battery performance, so it is rarely used in FSZABs.Second, metal meshes and metal foams have high conductivity, large porosity, and high mechanical strength, which benefits the diffusion of reactants and oxygen to active sites, thus improving battery performance.However, metalbased substrates are generally less stable due to fatigue during the bending, twisting, and stretching process.In addition, the high weight of the metal-based substrates increases the mass weight of the battery, which reduces the actual energy density of the battery.
In fact, researchers tend to use carbon-based substrates with light weight, excellent mechanical flexibility, high conductivity, excellent deformability, easy fabrication, and high porosity, including carbon paper (CP), carbon cloth (CC), carbon nanofiber film (CNF), carbon nanotube film (CNT), carbon fiber paper (CFP), and graphene oxide paper (GO). [26]First, the available commercial CC, CP, and CFP substrates have been applied widely in FSZABs, but the performance is not very ideal.Second, the CNF-based films prepared by electrospinning technology shows the advantages of adjustable components and excellent mechanical flexibility, which shows improved battery performance compared to commercial carbon materials.At the same time, graphene can also promote the battery performance due to its high specific surface area, excellent conductivity, and tolerance under severe working conditions.More importantly, CNTs have been considered as the most ideal substrates for self-supported air electrodes due to their large surface area, outstanding mechanical strength, and abundant accessible pathways for mass transportation, thus possessing superior battery performance generally.

ORR and OER Mechanisms
ORR and OER with slow oxygen electrochemical reaction kinetics in the air electrodes can hinder the performance of FSZABs.Equation ( 5)-(10) represent the ORR that involves complicated reactions with multiple-electron transfer at the air cathode, where * represents the active site on the catalyst surface.These complex reactions are classified into two-electron (Equation ( 5) and ( 6)) and four-electron (Equation ( 7)-( 10)) transfer steps, respectively. [27]Compared to the four-electron transfer steps, the generation of peroxides in the former transfer steps usually leads to inadequate energy and stability.1a] Researchers usually prefer the four-electron transfer route of ORR for FSZABs.
The conventional adsorbate evolution mechanism (AEM) and the lattice-oxygen-mediated mechanism (LOM) for OER are depicted in Figure 3. First, the reaction process for the AEM is similar to ORR but in the opposite order (Figure 3a).A proportional relationship exists between the adsorption energies of the aforementioned oxygen-containing intermediates, resulting in a minimum 0.37 V overpotential for this mechanism. [28]ccording to Sabatier's theory, the oxidation of HO* becomes the rate-determining step at low binding energy.In contrast, the formation of HOO* becomes the rate-determining step when the binding energy is high. [29]Unlike the AEM, the LOM can avoid the formation of HOO* (Figure 3b).The lattice oxygen atom reacts with the adsorbed oxygen or combines with another lattice oxygen atom to form O─O bonds, thus bypassing the aforementioned overpotential limitation (0.37 V) caused by the proportional relationship between HO* and HOO*. [28,30]ased on these mechanisms, the redox ability of metal and oxygen ions during the OER processes determines which reaction mechanism occurred on the catalyst's surface.When the electron-transfer ability of metal ions becomes more substantial, the OER proceeds with the AEM mechanism, and the oxygencontaining reaction intermediate determines the overpotential.When the lattice oxygen atom is activated for the OER, the deprotonation ability of the oxygen-containing intermediate determines the OER rate. [29,31]
Then, to analyze the bifunctional electrochemical performance, the potential difference ΔE between the overpotential of OER and the half-wave potential of ORR generally can be calculated, where a smaller ΔE represents a better bifunctional electrochemical activity. [32]8a] 3. Self-Supported Air Electrodes for FSZABs Traditional air electrodes using powder electrocatalysts can improve the electrochemical performance and durability of ZABs.Table 1 summarizes the performances of recently developed powder catalysts for aqueous ZABs and FSZABs.These powder catalysts can be classified into 1) precious metal-based catalysts, 2) transition metal-based catalysts (metal alloys, oxides, hydroxides, nitrides, and phosphides), and 3) metal-free carbon catalysts.The performance of powder electrocatalysts can be modified through component modulation, structural modulation, size adjustment, morphology design, and composite construction, which show improved catalytic performance of aqueous ZABs.However, the evaporation and leakage of liquid electrolytes will inevitably decrease the lifetime of ZABs, and packaging limitation of liquid electrolytes also causes the excessive weight of batteries, which could not meet the requirements of wearable electronic devices.In contrast, the solid electrolyte in FSZABs can conduct ions, separate the electrodes, and support the flexible structures, which simplify the production process of batteries.In addition, the FSZABs possess higher safety, environmental friendliness, and flexibility, which show great potential for commercialization in flexible devices compared with aqueous ZABs.Obviously, the ionic conductivity of solid electrolyte is much lower than that of aqueous electrolyte, thus leading to lower battery performance of FSZABs than that of aqueous Zn-air batteries.
More importantly, the inherent properties of powder catalysts have limited the performance improvement of FSZABs: 1) the use of polymer binder blocks the transfer of electron and mass, lowering the ORR and OER activity of catalysts, and its degradation also leads to the shedding of the catalysts; 2) the addition of conductive carbon increases the weight of electrode by 10-40 wt% and reduces the battery energy density.In addition, the corrosion of carbon during the OER process also decreases the electronic conductivity and catalytic performance; 3) the agglomeration of powder catalysts is inevitable and the contact with the conductive substrates also is insufficient; 4) the powder catalysts are easily detached from the air electrodes during the mechanical stress test; and 5) the preparation process is complex and time-consuming.All above shortcomings eventually cause poor performance of powder-based FSZABs, especially the durability and flexibility.As shown in Table 1, the power density of powder-based FSZABs is generally less than 100 mW cm À2 , and cycling stability can only lasts for about 30 h under low current density.

Sandwich
Ni foam PVA 0.56/69.5% 74 mW cm À2 @61 mA cm À2 ; 713 mAh g À1 ; @5 mA cm À2 for 30 h [66]   CuCo 2 S 4 NSs@N-CNFs Sandwich CNTs PVA 0.72/64.7%232 mW cm À2 @280 mA cm À2 ; 896 mAh g À1 @25 mA cm À2 ; 965.2 Wh kg À1 @25 mA cm À2 ; 1.46 V; @5 mA cm À2 for 100 h [68]   Co 9 S 8 -NSHPCNF Sandwich HPCNF PVA 0.83/58.5% 62.6 mW cm À2 @92 mA cm À2 ; 1.338 V; @5 mA cm À2 for 30 h [69]  3.1.Metal-Free Carbon Materials High electronic conductivity, large specific surface area, and diverse morphologies are the unique characteristics of metal-free carbon materials used in self-supported bifunctional air electrodes for FSZABs.However, the ORR of these materials generally proceeds in a two-electron pathway (Equation ( 5) and ( 6)), leading to the aforementioned low energy efficiency and stability.At the same time, carbon materials possess poor OER activity and tend to oxidize and corrode at high OER potentials, reducing the stability and energy conversion efficiency of ZABs. [33]owever, studies have reported that doping heteroatoms (N, S, O, B, and P) can break the C─C bonds and promote electron transfer, thus optimizing active sites' adsorption-desorption characteristics. [34]Heteroatom doping on carbon substrates can also lessen their oxidative decomposition during the OER (charging) process. [35]A few recent studies have successfully developed self-supported bifunctional air electrodes using these heteroatom-doped carbon materials (metal-free) that can concurrently overcome the setbacks of ORR and OER, [34a,35a] including not only single but also binary or ternary heteroatom dopants.Li et al. [36] adopted a directed growth approach to developing 3D nitrogen-doped carbon nanotube (NCNT) arrays/Ni foam as self-supported bifunctional air electrodes, where their metal-organic frameworks (MOFs) serve as carbon and nitrogen source (Figure 4a).N-doping with strong electron affinity can increase the positive charge density of adjacent carbon atoms, enabling the O 2 adsorption and O═O bond breaking, thus speeding up the O 2 reduction rate in the aforementioned four-electron pathway (Equation ( 7)-( 10)). [37,38]As a result, with its uniform N-doping, unique hierarchical nanoarray structure (Figure 4b), and decreased charge transfer resistance, the developed 3D NCNT array could achieve an E 1/2 of 0.81 V (Figure 4c) and an η of 0.27 V (Figure 4d).

[12b]
Co/Co-N-C Cable Carbon felts PVA 0.72/62.7%1.41 V; @5.0 mA cm À2 for 10 h [141]  performed the density functional theory (DFT) calculations to reveal the reaction mechanism for this intertwined interface of CNTs-NC-CCC.With such interface bonding of CNT-NC, they managed to modulate the local charge density distribution and enhanced electron transfer, thus forming noticeable charge density differences compared to that of CNT þ CC (Figure 4h).The CNT-NC also exhibited a smaller energy barrier for ORR and OER than that of CNT þ NC at sites 1 and 2 (Figure 4i,j), thus acquiring a low ΔE of 0.78 V.In other words, the covalent coupling can develop a strong and stable interfacial connection between catalyst and substrate, increasing active sites and stabilizing the structure during the operation of ZABs.In short, we can consider interface engineering an efficient strategy to improve electrocatalysts' electrochemical activity and durability.
Codoping with different heteroatoms (other than N) can control the partial electronic structure and carbon polarity effectively, thus enhancing further the electrochemical activity and durability of the carbon materials. [40]Zhang et al. [41] successfully used defect-enriched porous graphene-like carbon nanomaterial with N, S atoms codoping (D-S/N-GLC) as an air electrode for the FSZAB (Figure 5a-c), which showed a peak power density of 81 mW cm À2 .Likewise, Wang et al. [42] motivated by this codoping strategy, successfully developed B, N, and F tridoped lignin-based interconnected carbon nanofibers (BNF-LCFs) electrodes via electrospinning and pyrolysis.They coadded ammonium fluoride and zinc borate to the BNF-LCFs to increase their porosity, holes, and defective structures (Figure 5d,e).In addition, their X-ray photoelectron spectroscopy (XPS) spectra and the calculated bar charts revealed that adding B and F could influence the concentration and species of N functional groups (Figure 5f-i), thus optimizing the carbon matrix's electronic structures and electrochemical properties.As a result, their samples exhibited excellent bifunctional activity toward ORR and OER with a small ΔE of 0.73 V.Moreover, the FSZAB assembled with BNF-LCFs could deliver an OCV of 1.36 V and display impressive cycling stability for 13 h.

Transition Metals and Compounds/Conductive Substrates
Although the aforementioned heteroatom-doped metal-free carbon materials can act as self-supported air electrodes to relieve carbon decomposition during the OER (charging), this oxidative decomposition cannot be avoided entirely, notably during a and ORR and OER performance (c,d), respectively.a-d) Reproduced with permission. [36]Copyright 2017, Elsevier.e) Schematic illustration for synthesis of CNTs-NC-CCC and their corresponding f,g) SEM and TEM images, h) spin-charge density distribution of CNT þ NC and CNT-NC, and i,j) free energy diagrams of CNT þ NC and CNT-NC on site 1 (i) and site 2 (j) for ORR and OER, respectively.e-j) Reproduced with permission. [39]Copyright 2022, Elsevier.
long-term cycling test.This decomposition will cause the electrolyte turn yellow and severely reduce battery performance. [43]ence, transition metals and compounds have attracted much attention for developing stable catalysts by directly using them on the conductive carbon surface to replace metal-free carbon electrodes.These transition metals and compounds can be metals, alloys, metal oxides, sulfides, nitrides, and phosphides.16a,44,45] They can also mitigate electrochemical corrosion and carbon decomposition.In short, metal materials can also be employed as substrates for air electrodes to improve long-term cycling stability given their excellent stability.

Transition Metals
Conductive substrates can help to disperse active sites effectively and increase the electrochemical activity, thus preventing the agglomeration and corrosion of metal nanoparticles. [46,47]erefore, constructing transition metal nanoparticles on conductive substrates and N-doping to form self-supported bifunctional air electrodes can be an effective strategy to enhance battery performance.For instance, Lu et al. [48] successfully introduced cobalt (Co), N-codoped CNT arrays on carbon fiber cloth (CC-A-N@Co-NCNT) through a two-step in situ growth method (Figure 6a), [48] producing an air electrode with the best oxygen diffusion path and the shortest electron-transport path (Figure 6b), thus delivering superior flexibility and stability for ZABs.Similarly, Liu et al. [49] developed a 3D hierarchical porous electrode by combining in situ growth and deposition methods, producing Co/N@CNTs@CNMF-based FSZABs, where CNMF represents carbon nanotube microfilm.Their scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) images showed Co nanoparticles captured in bamboo-like N-doped CNTs on the CNMF surface (Figure 6c-e).As a result, their ZAB could deliver a high OCV of 1.40 V (Figure 6f ), a peak power density of 26.5 mW cm À2 , and a stable charge-discharge cycling curve at different bending angles (Figure 6g).c) Reproduced with permission. [41]Copyright 2017, American Chemical Society.d) TEM image of BNF-LCFs.e) Raman spectra of catalysts.f ) N 1s spectra of catalysts.g) The absolute content of various N species in catalysts.h) B 1s spectra of catalysts.i) The absolute content of various N species in catalysts.d-i) Reproduced with permission. [42]Copyright 2022, Elsevier.
Recently, zeolitic-imidazolate framework (ZIF) materials become popular among transition metals and compounds for developing bifunctional catalysts.ZIF, which consists of metal cations and imidazole ligands, displays ultrahigh specific surface area, high porosity, and structural flexibility advantages. [50]IF-derived porous carbon frameworks with unique morphologies of metal nanoparticles and/or N atom doping via the pyrolysis process play a vital role in transition metals and compounds.For example, Amiinu et al. [51] used 3D ZIF nanocrystals to obtain Ti foil for preparing a novel Co-N x /C.This bifunctional catalyst could demonstrate a low ΔE of 0.65 V for ORR and OER, a high OCV of 1.42 V, a high voltaic efficiency of 65.7%, and an excellent cycling stability for FSZABs.Such outstanding electrochemical activity can be ascribed to the presence of numerous active sites on the nanorods, increased surface area, and synergistic effect of the abundant Co-N coupling centers, which were confirmed by their XPS and DFT analysis results.
Similarly, constructing bimetallic alloys (Fe, Co, and Ni) on conductive substrates with N-doping can enhance the air electrodes' ORR and OER electrochemical activities through the electronic interactions between different metals. [52,53]For instance, Jin et al. [54] managed to encapsulate Co and FeCo nanowire arrays on N-doped carbon cloth (Co-FeCo/N-G-CC) as air electrodes for FSZABs.The superior electrochemical activity can be ascribed to the etching effect and plasma that enhanced the porosity and exposed more active sites for the Co-FeCo/ N-G-CC.Typically, the alloys can also be derived from MOFs during pyrolysis.Zhang et al. [55] successfully fabricated a bifunctional catalyst CoNi alloy/NCNSAs/CC with CoNi alloy and CNT decorated N-doped carbon nanosheet arrays on CC (NCNSAs/CC) (Figure 7a).The surface morphology revealed uniform impaction of CoNi nanoparticles and CNTs in the NCNS on CC (Figure 7b-d), thus giving enhanced bifunctional performance toward ORR and OER with a marginal potential difference of 0.68 V.This enhancement can be ascribed to the 3D hierarchical nanostructure, evenly dispersed active sites, and high graphitization degree.Furthermore, the FSZABs based on CoNi alloy/NCNSAs/CC as a self-supported air electrode demonstrated superior durability (Figure 7e), and higher powder density (98.8 mW cm À2 ) (Figure 7f ) and capacity (879 mAh h À1 ) than those of Pt/C/CC (Figure 7g).Reproduced with permission. [48]Copyright 2020, Wiley-VCH.c,d) SEM and e) HRTEM images of Co/N@CNTs@CNMF-800.f ) OCV test, and g) charge-discharge profiles of ZABs at different angles.c-g) Reproduced with permission. [49]Copyright 2020, Wiley-VCH.
On the other hand, combining atomic dispersion of metal atoms with heteroatom-doped conductive carbon substrates can be another effective strategy to optimize the utilization efficiency and electrocatalytic performance of FSZABs. [56,57]or instance, Wang et al. [58] pyrolyzed Cu 2þ -saturated brinjal slice to obtain a single Cu atom anchored O,N-doped porous carbon (SCu-ONPC) air electrode.Their DFT analysis revealed that the Cu-N 3 O species contributed to increased intrinsic activity both for ORR and OER.Interestingly, M-N x species anchoring in conductive carbon substrates often act as active sites for ORR and OER.They used an electrospinning method to disperse Co atoms and construct CNT-linked NCFs in Co SA/NCFs catalysts.Their SEM, transmission electron microscopy (TEM), X-ray absorption near edge spectroscopy (XANES), and extended X-ray absorption fine structure (EXAFS) analysis revealed the formation of randomly arranged 3D network structure (Figure 8a,b) and atomic-level dispersion of Co atoms in the form of Co─N bonds (Figure 8c,d).These observations support the excellent electrochemical performance. [59]imilarly, Yang et al. [60] combined electrospinning and pyrolysis to prepare a self-supported bifunctional air electrode by dispersing Fe-N 4 /C atomically on the carbon fiber membrane (Fe/SNCFs-NH 3 ) (Figure 8e).The SEM image showed the presence of abundant interconnected macropores formed by the intertwined carbon fibers (Figure 8f ), which facilitate gas transport, electrolyte infiltration, and electron transfer.Moreover, the EXAFS curves verified that Fe in Fe/SNCFs-NH 3 is atomically dispersed and coordinated with N/O (Figure 8g).Notably, doping of S atoms plays a vital role in modulating reaction barriers to improve ORR and OER processes.Copyright 2020, IOP Publishing Ltd.

Transition Metal Compounds/Conductive Substrates
Recently, transition metal-based oxides, sulfides, nitrides, phosphides, and selenides have been extensively explored as bifunctional oxygen electrocatalysts.However, the poor conductivity and low dispersion of these compounds in the powder form still hinder the catalytic improvement of ZABs.Thus, transition metal compounds are usually deposited onto conductive substrates surface overcome the aforementioned deficiencies.In particular, Co-, Fe-, and Ni-based single metal oxides, spinel oxides, and perovskite oxides have attracted much attention given their low cost, simple preparation, environmental compatibility, and natural abundance. [61]Studies showed that coating the transition oxides onto conductive substrates to obtain self-supported air electrodes with the novel nanostructure could increase the specific surface area, conductivity, durability, and electron transfer rate, and shorten the ion diffusion length. [62]o-based transition metal oxides, especially Co-based spineltype oxides, show excellent electrocatalytic activity given their excellent stability, multiple oxidation states of Co ions, and unique structure.Spinel Co 3 O 4 has two types of Co ions, i.e., Co 3þ ions at octahedral sites that promote the ORR and Co 2þ ions at tetrahedral positions that favor the OER process.However, their limited active sites, low specific surface area, and poor conductivity have severely limited their electrocatalytic activity.Hence, constructing the spinel Co 3 O 4 on carbon materials or using the conductive substrates to construct selfsupported air electrodes can be an efficient pathway for FSZABs.[62,63] Chen et al. [64] grew the ultrathin Co 3 O 4 layer on the carbon fibers horizontally and uniformly by electrodeposition followed by annealing treatment (Figure 9a).The surface morphology showed the presence of mesopores in the Co 3 O 4 layer and ultrathin Co 3 O 4 layer (5 nm) (Figure 9b-d), resulting in an optimized electrical contact area and strong adhesion on the conductive support.As a result, the FSZAB exhibited excellent mechanical stability and safety under severe conditions (Figure 9e-g).Yu et al. [23b] managed to fabricate N-doped Co 3 O 4 nanowires on CC through hydrothermal and sequential annealing, giving a high 98.1 mAh cm À3 volumetric capacity and flexibility with its air electrode for the FSZABs.Their results confirmed that N-doping in Co 3 O 4 could also enhance the electronic conductivity, O 2 adsorption strength, and reaction kinetics, thus improving the overall electrochemical activity.These excellent outcomes highlight its practical suitability for flexible and wearable electronics application.
Another common strategy to develop self-supported air electrodes for FSZABs is through in situ synthesis of array structures such as hydrothermal, chemical, or electrochemical with subsequent pyrolysis.These array structures with orientated growth and high surface area are constructed on the conductive carbon surface or metal substrates, improving the close contact of the components in the air electrode and promoting oxygen and electrolyte diffusion to reach the active catalytic site efficiently, consequently accelerating the oxygen reaction process.At the same time, direct growth of bifunctional catalysts on flexible substrates can benefit fast electron transfer, good conductivity, and structure stability, enabling high-performance ZABs. [65]gure 8. a) SEM and b) TEM images of Co SA/NCFs.c) Fourier transforms and d) WT analysis of EXAFS spectra for samples.a-d) Reproduced with permission. [59]Copyright 2022, American Chemical Society.e) Schematic illustration of the synthesis and f ) SEM image of Fe/SNCFs-NH 3 .g) Fourier transforms of EXAFS spectra of samples.h) Charge-discharge profiles of catalysts.e-h) Reproduced with permission. [60]Copyright 2022, Wiley-VCH.
Therefore, Fu et al. [44] embedded Co 3 O 4 nanoparticles in NCNT arrays on the stainless steel (SS) mesh surface, developing a unique morphology structure similar to human hair arrays (Figure 10a).Benefiting from this hair-like structure (Figure 10b-d) and synergistic effects between Co 3 O 4 and NCNT, the Co 3 O 4 -NCNT arrays can be coupled with SS mesh without sacrificing interfacial contact.Hence, these arrays enabled high electrical conductivity, boosting electrocatalytic active sites and preventing Co 3 O 4 -NCNT from restacking and detaching.As a result, the Co 3 O 4 -NCNT/SS-based FSZAB could yield a high specific capacity of 652.6 and 632.3 mAh g À1 at 5 and 50 mA cm À2 , respectively (Figure 10e), excellent rechargeable stability (Figure 10f ), and robust mechanical integrity (Figure 10g).
Moreover, introducing metal cations as in the case of Co-based spinel oxides with nanostructure can also enrich the active sites.16a] Besides, the Ni atom radius of 149 pm is close to that of Co of 152 pm, making it easy to access the crystal cell of Co 3 O 4 and weaken the lattice alkalinity.For example, Xu et al. [66] deposited (Ni,Co) 3 O 4 oxide onto Ni foam to construct self-supported air electrodes for FSZABs.Their SEM images revealed consistent growth of (Ni,Co) 3 O 4 nanosheet arrays in Ni form with many pores in (Ni,Co) 3 O 4 , allowing the oxygen and electrolyte access during the electrochemical reaction process (Figure 10h,i).Then, their DFT calculation revealed the ORR and OER mechanisms (Figure 10j,k).As for the OER, the rich defect sites in (Ni, Co) 3 O 4 nanosheet arrays accelerated the adsorption of reactants.During the ORR, the Ni-doping in Co 3 O 4 lowered the surface activity toward O, OH, and OOH species, further keeping the OOH molecular state without dissociation on the surface, thus improving the ORR activity.As a result, this self-supported electrode yielded a lower charge-discharge gap of 0.56 V, a large specific volumetric energy capacity of 2268 mW h cm À3 , as well as a high specific energy capacity of 686 mW h g À1 .
Recent studies have shown that self-supported bifunctional air electrodes were successfully developed using transition metal chalcogenides/conductive substrates. [67,68]This can be attributed to their suitable binding energy to intermediates reaction, favorable electrical conductivity, and corrosion resistance.Peng et al. [69] embedded Co 9 S 8 nanoparticles in N/S dual-doped  and c,d) TEM images and their corresponding elemental mapping.e) Galvanostatic charge-discharge test results of the FSZABs in the panel under various bending radii of 51, 28, and 13 mm.f,g) Photographs of a working integrated device during the cutting process.a-g) Reproduced with permission. [64]Copyright 2017, Wiley-VCH.
hollow and porous carbon nanofibers through electrospinning followed by reoxidation and carbonization treatment.Due to the unique structure, dual doping of N and S atoms, enhanced electrical conductivity, and high specific surface area, the asprepared Co 9 S 8 -NSHPCNF yielded an E 1/2 of 0.82 V for ORR and η of 0.35 V for OER, outperforming the precious metal-based catalysts.Liu et al. [70] designed a 3D NiCo 2 S 4 nanoarrays with defect-enriched N-doped GQDs (N-GQDs) on CC as a bifunctional air electrode.Their DFT calculations revealed that the stronger the OOH* dissociation adsorption at the interface between N-GQDs and NiCo 2 S 4 , the lower the overpotential between ORR and OER.Hence, given its unique morphologies and high conductivity, the CoSe 2 catalyst plays a vital role in transition metal chalcogenides.
To obtain self-supported bifunctional air electrodes for FSZABs, Zhang et al. [63] prepared hierarchical flake arrays of N-doped carbon flakes embedded with P-doped CoSe 2 on CC (Figure 11a).Such hierarchical flake arrays in P-CoSe 2 /N-C (Figure 11b) displayed an E 1/2 of 0.87 V for ORR (Figure 11c) and η of 0.23 V for OER (Figure 11d).In addition, the FSZAB yielded a high OCV of 1.30 V and good mechanical flexibility (Figure 11e).These much-enhanced electrocatalytic performances can be ascribed to the synergistic interaction of the multilevel controls in the structure as well as the optimized electronic structure resulted by P-doping.With the exception of metal chalcogenides, combining transition metal nitrides with conductive substrates has also led to the outstanding activity of ORR and OER.Their excellent electron transfer ability and abundant elemental oxidation states played great significance in regulating the adsorption energy and conductivity.
Except for the metal chalcogenides, the combination of transition metal nitrides with conductive substrates has also been proved with superior ORR and OER activity because of their excellent electron transfer ability and abundant elemental valence states, which is of great significance for regulating the adsorption energy and conductivity. [71]Song et al. [72] successfully grown hierarchically porous cobalt nitride hybrid nanosheets on Ni foam (CoN@NC) via a novel vaporization-nitridation synthesis strategy (Figure 11f ).The TEM and HRTEM images (Figure 11g, h) verified the embedding of CoN nanoparticles in amorphous NC layer with abundant pores.The extended XAFS spectra in Figure 11i demonstrated the transformation of Co─O bond into Co─N in CoN@NC-300 after nitridation treatment, which is consistent with the results of the wavelet transform analysis (Figure 11j-l).With this 3D hierarchical porous architecture and strong coupling effect between CoN and NC, the flexible catalyst yielded an OCV of 1.47 V, a power density of 36.68 mW cm À2 , a specific capacity of 680 mAh g Zn À1 , and good cycling stability.Similarly, the codoped Fe-Co 4 N@N-C nanosheet array derived from MOFs could also yield high electrochemical activity for ORR (E 1/2 of 0.83 V) and OER (E 10 of 1.62 V). [73] The abundant pyridinic-N-M active sites for ORR and the enriched Co 3þ sites for OER in Fe-Co 4 N@N-C boosted the reaction kinetics.As a result, the FSZAB employing such air electrodes could yield a high volumetric power density of  [44] Copyright 2016, Wiley-VCH.h) SEM and i) TEM images of (Ni, Co) 3 O 4 @Ni foam.j) Free energy diagrams of OER and ORR on the Co site surface of Co 3 O 4 (001) at the U = 0 V. k) Free energy diagrams of OER and ORR on the Co site surface of Ni-doped Co 3 O 4 (001) at the U = 0 V. h-k) Reproduced with permission. [66]Copyright 2020, Elsevier.bending states.

Other Catalysts
Combining the advantages of two or more materials by structural design on the substrate's surface can concurrently improve air electrodes' electrochemical activity and stability.][76][77] Among them, combining two types of transition metal oxides to develop self-supported air electrodes has been proven promising. [74]For example, Wu et al. [78] synthesized a self-supported sandwich structured electrode by pressing two electrodes (NF@Co 3Àx Ni x O 4 and SS@Co 3 O 4 ) together.Their XAFS measurement revealed that the doping of Ni in Co 3 O 4 could change the local geometry and electronic structure of Co 3 O 4 .With this sandwich structure, the electrode yielded a high energy efficiency of 62.2% at a 5 mA cm À2 current density for FSZABs.
On the other hand, the rare-earth metal oxide modification strategy has been applied to construct highly efficient and ultrastable electrodes for FSZABs. [79]Hence, an Fe 3 O 4 /Eu 2 O 3 @NCG (denoting GO-doped carbon layer as NCG) electrode was synthesized by employing layered Fe-Eu MOF/GO (Fe-Eu-MOF/GO) as a precursor (Figure 12a).A solid-state ZAB based on such a  [63] Copyright 2018, Wiley-VCH.f ) Schematic illustration of the synthesis process of CoN@NC.g) TEM and h) HRTEM images of CoN@NC-300.i) Fourier transform extended XANES spectra and j-l) wavelet transforms of CoO (j), Co precursor (k), and CoN@NC-300 (l).f-l) Reproduced with permission. [72]Copyright 2022, Elsevier.
catalyst delivered a high peak power density and energy density of 92.7 mW cm À2 (Figure 12b) and 854 W h kg À1 (Figure 12c), respectively, and excellent charge-discharge cycling stability for 460 h (Figure 12d).Based on their DFT calculation to comprehend the origin of the outstanding activity of this catalyst, the d-band center of Fe 3 O 4 /Eu 2 O 3 @NCG (À5.365 eV) was located further away from the Fermi level than that of Fe 3 O 4 @NCG (À4.548 eV) (Figure 12e,f ), which could promote the desorption of O 2 .In addition, the density of the state value was larger, suggesting a fast electron transfer rate. [79]oreover, layered double hydroxides (LDHs) usually display superior OER activity due to their large interlayer spacing for mass transport to promote the oxygen reaction.Consequently, combining LDHs with transition metal oxides to construct self-supported bifunctional composite air electrodes is an attractive approach.Zhang and co-workers [80] prepared a NiCo 2 O 4 @NiMn LDH core-shell array on Ni foam by the deposition-calcination-deposition processes (Figure 12g).The TEM and HRTEM images were applied to characterize the morphology difference between NiCo 2 O 4 and NiCo 2 O 4 @NiMn LDH.Unlike the pure NiCo 2 O 4 nanowires (Figure 12g,h), NiMn LDH nanoflakes uniformly covered the NiCo 2 O 4 nanowires surface in NiCo 2 O 4 @NiMn LDH core-shell array (Figure 12i,j).With this unique structure, high active surface area, rapid mass/charge transport, and excellent electronic conductivity, the FSZAB employing this catalyst exhibited outstanding mechanical properties, long cycle durability, and high round-trip efficiency (70-74%).

Synthesis Strategies
Here, we summarize a few critical features that an ideal self-supported air electrode must have for FSZABs: 1) high electronic conductivity, which is generally achieved through the conductive substrate and the large, intimate interfacial contact between the conductive substrate and the catalysts; 2) high specific surface area and abundant pores for exposure to the active sites and ensuring the efficient accessibility to oxygen and the electrolyte; 3) chemical and physical stabilities such that the electrode material is not prone to oxidation and decomposition during the testing process, ensuring the long-term chargedischarge cycling stability for the battery; 4) the uniform dispersion of catalyst on conductive substrate surface with a tight contact; 5) novel nanostructure and morphology to achieve the hydrophobicity for the air electrode; 6) superior ORR and OER activity and stability; and finally 7) the robust contact between catalyst and substrate that enables fast electron transfer, excellent long-term durability and flexibility under battery charging-discharging cycles.
As a result, different preparation methods have been developed and applied to develop such highly active and stable self-supported air electrodes for FSZABs.Moreover, different catalytically active substances have also been extensively studied and prepared.Copyright 2022, American Chemical Society.g) Schematic illustration of the synthesis process of NiCo 2 O 4 @NiMn LDH on Ni foam.h-k) HRTEM images of NiCo 2 O 4 nanowires (h,i) and NiCo 2 O 4 @NiMn LDH.(j,k).g-k) Reproduced with permission. [80]Copyright 2018, The Royal Society of Chemistry.

Pyrolysis
The pyrolysis process generally requires pregrowth of the catalysts on the conductive substrate via the in situ growth, self-assembly, and freeze-drying processes, which ensure the construction of the catalyst/substrate interface and prevent the agglomeration of the catalysts.Subsequently, such substrates loading catalysts are heated at a specific temperature (600-900 °C) in the presence of carbon and heteroatomic sources (N, B, P, and S), thus forming self-supported air electrodes. [36,39,41,77]For example, a selfsupported air electrode iron phthalocyanine||NiFe 2 O 4 /G (FePc|| NiFe 2 O 4 /G) was obtained by pyrolysis, and a self-assembly strategy was used to pregrow the Prussian blue analogue (PBA) catalyst on the substrate GO surface (as carbon sources and metal sources). [81]Copyright 2023, Elsevier B.V. b) Reproduced with permission. [83]Copyright 2023, Royal Society of Chemistry.c) Reproduced with permission. [49]Copyright 2020, Wiley-VCH.d) Reproduced with permission. [89]Copyright 2020, Elsevier.e) Reproduced with permission. [74]Copyright 2022, Elsevier.
In addition, single-atom (SA) metal or alloy catalysts/ substrates developed by metal and heteroatom doping usually display excellent ORR and OER performances.Such air electrodes can also be prepared via pyrolysis, where MOFs, ZIFs, and COFs materials are often used as pyrolysis precursors. [36,79]The performances of pyrolysis-made single-atom metal or alloy catalysts/substrates, such as Co-N x /C/Ti, CoNi alloy NCNSAs/CC, and SAFe-SWCNT [57] were explored recently.The tight contact between the catalysts and conducting substrates can facilitate electron transfer and improve the dispersion of the catalyst, thus facilitating the reaction process.

Hydrothermal/Solvothermal
Despite their identical working principle, if the reaction medium used is water, the process is called hydrothermal.On the other hand, if organic solvent is used as the reaction medium, the process is termed solvothermal.The reaction temperature may vary between 80 and 250 °C, giving a high temperature and pressure environment within a sealed Teflon-lined autoclave, which allows the metal ions in the solution to recrystallize on the conductive substrate surface to obtain the self-supported air electrodes.Generally, air electrodes with different nanostructures and morphologies can be obtained by changing the metal ions, polar functional groups, and conductive substrates in the hydrothermal/solvothermal process.The uniform growth of the catalyst on the conductive substrate surface can increase the contact tightness, thus ensuring good electrical conductivity and mechanical stability. [82]ydrothermal/solvothermal processes have the advantages of mild reaction, low emission, and high catalyst purity.Moreover, hydrothermal/solvothermal process can also be combined with pyrolysis to make the ideal air electrodes (Figure 13b). [83]esearchers have recently developed self-supported air electrodes, such as NiCoO x /NF, [83] MPZCC@CNT, [46] Co 3 O 4 @NiFe LDH/NF, [45] NiO@Co 3 S 4 /NF, [84] CoN-Nd/CC, [85] and NF/Cu 0.76 Co 2.24 O 4 /FeCo hydroxides (NF/CCO/FCH), [86] all of which exhibited excellent ORR, OER, and battery performances.For example, Yang et al. [86] obtained an excellent air electrode via a two-step hydrothermal process.The FCH nanosheets formed in the second hydrothermal step uniformly modified the thin CCO nanosheets to obtain NF/CCO/FCH.Because of its unique heterogeneous structure, large three-phase interfacial area, multiple reaction sites, and excellent electron transfer capability, the air electrode yielded a low ΔE 0.66 V.The resultant FSZAB displayed a power density of 35.2 mW cm À2 , an OCV of 1.40 V, an initial round-trip efficiency of 71.6%, and an excellent cycling stability.

Vapor Deposition
The vapor deposition strategy mainly includes chemical vapor deposition (CVD) and physical vapor deposition (PVD).The CVD process involves the chemical decomposition reaction of precursor materials (including metallic materials and heteroatomic sources) under high temperatures (800-1000 °C) to form gaseous products, which are subsequently deposited onto the surface of conductive substrates to give self-supported air electrodes (Figure 13c). [49]So far, the researchers have prepared various metal/CNTs as self-supported air electrodes via CVD by utilizing the catalytic effect of transition metal nanoparticles (Co, Fe, and Ni) for the growth of CNTs under high temperatures (700-900 °C), [87] such as Co/N@CNTs@CNMF, [49] FeNi@NCNT@CC, [52] CoO@PCNAs@CC (denoting porous carbon nanosheets arrays as PCNAs), [88] and NP-VANCT-GF (denoting vertically aligned CNTs as VANCTs). [65]The FSZABs using them as self-supported air electrodes all yielded high power and energy densities and exhibited excellent charge-discharge cycling stability.
Unlike the CVD, the PVD process generally does not involve chemical reactions.Several methods, such as plasma engineering and magnetron sputtering, can be used to obtain the electrodes.Plasma engineering is a special plasma-liquid system that applies excited electrons and free radicals for rapid material synthesis.The utilized synthesis speed could reach about 10 mg min À1 , thus having an enormous application potential. [54,89]For example, Chen et al. [89] designed and prepared Fe-enriched FeNi 3 intermetallic nanoparticle/N-doped carbon (Fe-enriched FeNi 3 /NC) electrode based on plasma engineering (Figure 13d).The excess Fe ions induce a high degree of lattice distortion in this electrode, which results in abundant oxygen defects and promotes a higher active electron density around the Fermi energy level.As a result, the catalyst Fe-enriched FeNi 3 /NC outperformed the benchmark 20 wt% Pt/C þ Ir/C electrocatalyst with low potential difference (ΔE = 0.80 V), low charge-discharge voltage gap (0.89 V), high peak power (89 mW cm À2 ), as well as superior specific capacity of 734 mAh g Zn À1 at a 20 mA cm À2 .

Electrospinning
This technique is generally combined with carbonization process to obtain self-supported air electrodes for FSZABs.(Figure 13e). [74]First, the electrostatic repulsion between surface charges manifested into the production of 1D nanofibers from polymer solutions.The morphologies and sizes of these nanofibers can be constructed by changing the composition and content of transition metal ions and dopants in polymer solutions.Then, the subsequent processes, such as carbonization and/or oxidation and/or heteroatom (N, B, P, and S) doping, can be applied to obtain self-supported air electrodes with different structures (core-shell, hollow, and solid structures) and compositions with heteroatom doping (single-atom, oxide, and sulfide). [68,69]his strategy can be applied to modulate the composition, morphology, conductivity, specific surface area, and electronic structure of the electrodes, ensuring large specific surface area, abundant porosity, multiple active sites, and excellent mechanical strength, thus improving the energy density, cycling stability, and flexibility of ZABs. [59,76]The single-atom catalysts/ conductive substrates prepared via electrospinning tend to possess high electrochemical activity and durability. [56,60]or example, the air electrode Co SA@NCF/CNF synthesized by the electrospinning-impregnation-carburization processes could yield a half-wave potential of 0.88 V for ORR and an overpotential of 0.4 V for OER.Furthermore, the FSZAB based on Co SA@NCF/CNF could yield a specific capacity of 796 mAh g Zn À1 , an energy efficiency of 67.57%, and good stability.Such superior performance could be ascribed to the atomic-level dispersion of Co, the hierarchical porous structure, and the construction of a CNT, which guarantees the active site's accessibility and improves the electrodes' mechanical stability. [59] Summary and Outlook By virtue of high energy density, mechanical flexibility, low cost, and high safety, FSZABs will play a key role in flexible electronics application.Developing and designing robust self-supported bifunctional air electrodes is essential to the achieve high energy efficiency and good cycling stability in FSZABs.Electrocatalytic reactions in air electrodes involve the opposite ORR and OER processes, where O 2 diffusion, electron transfer, ion transport, and catalyst deactivation occur concurrently.An ideal self-supported air electrode should have enhanced electrical conductivity, abundant active sites, superior stability, and mechanical flexibility.Significant progresses in the design of such electrodes have been made recently that translate to the improvement of performance and durability of FSZABs.At the same time, arrays of advanced characterization techniques have also been employed to investigate the origin of the electrochemical activity.Furthermore, the appropriate synthesis strategy is also vital in developing self-supported air electrodes.Various processes, i.e., pyrolysis, hydrothermal, chemical vapor deposition, physical vapor deposition, and electrospinning, are available, which provide pathways to create unique catalysts' structure, morphology, size, and dispersity.Such tailoring, in turn, allows adjustment of the electrochemical activity and durability of the air electrodes.This review highlights the recent development of typical selfsupported bifunctional air electrodes (metal-free carbon materials, transition metals/conductive substrates, transition metal compounds/conductive substrates, and other air electrodes), including the structural design, performance optimization, synthesis strategies, and their application in FSZABs.Several studies have indicated that the use of self-supported bifunctional air electrodes in FSZABs could improve the round-trip efficiency, energy density, OCV, and cycling durability.However, the performance and long-term cycling life of FSZABs are still far from commercialization expectation compared to aqueous ZABs.We listed below the considerable scientific and technological challenges that need to be overcome for further practical applications.1) The performance of FSZABs at this stage still cannot meet the requirements of commercial flexible and wearable electronic devices.The low round-trip efficiency, power density, and short cycling stability are still unsatisfactory.The development of self-supported bifunctional air electrodes is the most critical factor that determines the ORR, OER, and battery performances.The air electrodes are composed of active catalysts and conductive substrates.The selection of active catalysts should mainly focus on intrinsic activity, stability, conductivity, and hydrophilicity/hydrophobicity.Besides, the substrates should possess high electronic conductivity, mechanical flexibility, lightweight, and anticorrosion simultaneously.The strong interaction and abundant intimate contact between catalyst and substrate ensure good long-term durability and flexibility, suppressing the detachment of active catalysts.Furthermore, the facile and scalable synthesis strategy is also essential in lowering the cost of FSZABs.2) Advanced theoretical calculations and characterization methods are important for exploring reaction mechanisms and performance improvement.First, DFT calculation can provide insights into the OER and ORR mechanisms and how to further enhance the electrochemical activity and stability.However, the structure of selfsupported air electrodes may be complex due to the simultaneous inclusion of catalyst and substrate, making the construction and optimization of crystal models challenging.Second, traditional characterizations have mainly focused on catalysts' structure, morphology, electronic states, and the catalytic mechanisms for ORR and OER.However, the interaction of catalysts and substrates, their structural changes during the reaction, and their influence on the ZAB performance and durability have not been studied in detail.
3) A more systematic evaluation criterion for FSZABs is necessary for comparison.First, different indicators criteria or forms in terms of specific capacity, energy density, and/or cycle stability have been used to evaluate battery performance in the literature, making it difficult to compare them.In addition, most literature only provides battery performance at low current density (<20 mA cm À2 ), which fails to meet the requirements of practical applications (>50 mA cm À2 ).Finally, mechanical stability cannot be overlooked for the application of solid-state ZABs in flexible devices.However, most works only show the cycling stability at some bending angles to prove the flexibility of the battery, which may not be enough to evaluate the mechanical stability and flexibility of the ZABs.4) In addition to using self-supported air electrodes and solid electrolytes, optimizing other components for solid-state ZABs can also be critical for their application in wearable/foldable electronic devices.For example, the parasitic reaction between Zn and electrolytes and the formation of Zn dendrites can reduce the availability of active sites and the battery lifetime.Studies have shown that Zn anodes' surface or composition modification can effectively resolve this dilemma.In addition, the structure and assembly technology of solid-state ZABs is also essential for their application in practical devices.

Figure 4 .
Figure 4. a) Schematic illustration of the synthesis of 3D NCNT arrays by a facile-directed growth process and b-d) their corresponding TEM image (b)and ORR and OER performance (c,d), respectively.a-d) Reproduced with permission.[36]Copyright 2017, Elsevier.e) Schematic illustration for synthesis of CNTs-NC-CCC and their corresponding f,g) SEM and TEM images, h) spin-charge density distribution of CNT þ NC and CNT-NC, and i,j) free energy diagrams of CNT þ NC and CNT-NC on site 1 (i) and site 2 (j) for ORR and OER, respectively.e-j) Reproduced with permission.[39]Copyright 2022, Elsevier.

Figure 5 .
Figure 5. a,b) TEM images and c) Raman spectra of D-S/N-GLC.a-c) Reproduced with permission.[41]Copyright 2017, American Chemical Society.d) TEM image of BNF-LCFs.e) Raman spectra of catalysts.f ) N 1s spectra of catalysts.g) The absolute content of various N species in catalysts.h) B 1s spectra of catalysts.i) The absolute content of various N species in catalysts.d-i) Reproduced with permission.[42]Copyright 2022, Elsevier.

Figure 7 .
Figure 7. CoNi alloy and CNT decorated N-doped carbon nanosheet arrays on carbon cloth.a) Schematic illustration of the synthesis process.b) SEM images.c,d) HRTEM images.e) Galvanostatic discharge profiles at different current densities.f ) Power-current density profiles.g) Voltage-capacity profiles.a-g) Reproduced with permission.[55]Copyright 2020, IOP Publishing Ltd.

Figure 9 .
Figure 9. a) Schematic illustration of the ultrathin Co 3 O 4 /CC synthesis process.b) SEMand c,d) TEM images and their corresponding elemental mapping.e) Galvanostatic charge-discharge test results of the FSZABs in the panel under various bending radii of 51, 28, and 13 mm.f,g) Photographs of a working integrated device during the cutting process.a-g) Reproduced with permission.[64]Copyright 2017, Wiley-VCH.

Figure 10 .
Figure 10.a) A schematic illustration of a hair-like array of Co 3 O 4 -NCNT/SS air electrode.b,c) SEM and d) TEM images of Co 3 O 4 -NCNT/SS.e) Specific capacity, f ) charge-discharge, and g) polarization profiles at different bending angles of Co 3 O 4 -NCNT/SS-based ZAB.a-g) Reproduced with permission.[44]Copyright 2016, Wiley-VCH.h) SEM and i) TEM images of (Ni, Co) 3 O 4 @Ni foam.j) Free energy diagrams of OER and ORR on the Co site surface of Co 3 O 4 (001) at the U = 0 V. k) Free energy diagrams of OER and ORR on the Co site surface of Ni-doped Co 3 O 4 (001) at the U = 0 V. h-k) Reproduced with permission.[66]Copyright 2020, Elsevier.

Figure 11 .
Figure 11.a) Schematic illustration of the synthesis process of P-CoSe 2 /N-C arrays.b) SEM image of P-CoSe 2 /N-C.c) ORR and d) OER profiles and e) digital images of the OCVs and LEDs powered by P-CoSe 2 /N-C-based ZAB at different bending angles.a-e) Reproduced with permission.[63]Copyright 2018, Wiley-VCH.f ) Schematic illustration of the synthesis process of CoN@NC.g) TEM and h) HRTEM images of CoN@NC-300.i) Fourier transform extended XANES spectra and j-l) wavelet transforms of CoO (j), Co precursor (k), and CoN@NC-300 (l).f-l) Reproduced with permission.[72]Copyright 2022, Elsevier.

Table 1 .
The OER, ORR (in a 0.1 M KOH), and catalytic performances of recently developed powder catalysts for aqueous ZABs and FSZABs.

Table 2 .
The FSZABs performances based on recently developed self-supported bifunctional air electrodes.