A Decade of Electrocatalysis with Metal Aerogels: A Perspective

Abstract

Nowadays, great efforts have been spent on addressing concerns over energy and environmental crises. Among these efforts, electrocatalysis is widely recognized and studied for its high efficiency and easy processability. As a class of emerging electrocatalysts, metal aerogels (MAs) stand out in the last decade. In virtue of their three-dimensional conductive pathways, their library of catalytically/optically active sites, and their robust network structures, MAs have unique advantages in electrocatalysis. However, due to the short history of MAs, there is insufficient research on them, leaving significant room for material design and performance optimization. This perspective will mainly focus on electrocatalysis with MAs, aiming to summarize the state-of-the-art progress and to guide the on-target design of efficient MAs-based electrocatalysts towards energy- and environment-related applications.

1. Introduction

Electrocatalysis plays a critical role in diverse energy- and environment-related processes, such as the oxygen reduction reaction (ORR) and the fuel oxidation reaction (e.g., the alcohol oxidation reaction (AOR) and the hydrogen oxidation reaction (HOR)) in fuel cells [1,2,3,4], the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) in water splitting [5,6,7], and the carbon dioxide reduction reaction (CO₂RR) in producing high value-added chemicals [8,9]. Besides a high efficiency, the electrochemical process can flexibly utilize the stored electricity generated from renewable energy, thus alleviating the energy crisis resulting from the excessive use of fossil fuels. Therefore, to promote these electrochemical processes, the development of high-performance electrocatalysts is central for both the scientific and the industrial community.

In principle, efficient electrocatalysis calls for abundant accessible active sites, high single-site activity, high electrical conductivity, and reasonable cost. In the past several decades, a wide range of materials, including metals, metallic compounds (e.g., metal oxides and metal dichalcogenides), nanocarbons, and various composites, have been extensively investigated as electrocatalysts [10,11,12,13,14,15,16]. In particular, nanostructuring can endow original bulk materials with a large specific surface area (SSA), high reactivity, and dramatic size effects, thus promoting their performance. While significant advances have been achieved in the creative synthesis of nanomaterials, the intrinsic instability of this nano-sized matter and the relatively poor electrical connection pose difficulties in achieving high-performance and robust electrocatalysis. In this regard, the exploration of new catalysts is of paramount importance.

Metal aerogels (MAs), a new class of porous materials developed in 2009 [17,18], are promising for addressing the aforementioned issues. As these aerogels are entirely built up by nanostructured metals, MAs inherit the unique physicochemical properties of metals (e.g., catalytic activity, electrical conductivity, and special optical properties) and structural features of aerogels (e.g., porous network, large SSA, and monolithic architecture) [19,20]. In this light, featuring numerous active sites, rapid mass/electron transfer pathways, robust structure, and tunable compositions, MAs manifest unprecedented potential as highly active and durable electrocatalysts, overwhelming conventional non-metal and unsupported metallic catalysts [21]. Despite these unique attributes, the development of MAs has not been smooth, particularly in their early years, which can be attributed to an insufficient materials basis resulting from their unconventional formation behavior, immature fabrication methods, and less-explored physicochemical properties [22,23]. In this regard, the corresponding application studies, such as those for electrocatalysis, have inevitably been slowed down. Although quite a few synthesized MAs have been proven to efficiently catalyze diverse electrochemical processes [22,23,24,25], their design principles are not clear, and their performance needs further improvement.

In the past few years, several reviews have summarized the controlled synthesis of MAs and/or their analogs, as well as their diverse applications [19,26,27]. However, an overview dedicated to the on-demand design of MAs for electrocatalysis is absent. Additionally, the recent research progress for MAs may inspire new insights into this topic. From this perspective, we will first summarize the synthesis of MAs from a historical view. In the following sections, electrocatalysis with MAs for fuel oxidation reactions, oxygen-related reactions, hydrogen-related reactions, and other electrochemical processes will be sequentially discussed. Finally, the challenges and opportunities associated with MAs for electrocatalysis will be summarized to guide the on-target engineering of MAs as efficient electrocatalysts.

2. A Brief Overview of Metal Aerogel Synthesis

Strictly speaking, aerogels are materials derived from a sol-gel process followed by special drying [28]. In this context, special drying usually refers to freeze-drying or supercritical drying, which is used to transfer as-formed wet gels to aerogels. The use of special drying can alleviate the structural collapse incurred by the strong capillary forces generated around the gel network during the drying process, which is realized either by fixing the solid network via freezing (i.e., freeze-drying process) or by transforming the solvent into the supercritical state (i.e., supercritical drying process) before removing it.

MAs are usually defined as free-standing all-metal-made aerogels obtained in the same way as mentioned above. So far, most reported MAs are structured from noble metals, which, however, only account for less than 10% of all metal elements in the periodic table. This is probably because of their relatively higher redox potential compared with other metals, which leads to an easy synthesis, as well as the high stability of the derived noble MAs. Apart from the limited compositions, the synthesis and applications of MAs are also severely hindered by the shortage of structure controllability. As mentioned above, MAs are usually prepared by sequential gelation and drying process. Since the drying method is mature, attention is often paid to the design of the sol-gel process. Usually, depending on whether a separate metal nanoparticle (NP) formation step is involved or not, the gelation methods are divided into two-step and one-step strategies. Following this classification, this section will summarize the state-of-the-art fabrication methods of MAs.

In the early studies on MAs, the two-step strategy was adopted at first, where the sol-gel process undergoes separate metal NP formation and the wet gel formation stage [18,29,30]. Initiated by Bigall et al. in 2009, Au, Ag, Pt, Au-Ag, and Pt-Ag (Figure 1a) aerogels were synthesized by an oxidation-triggered two-step method [18]. In short, the concentrated noble metal NP solutions (the concentration of the metal salts c_M = 10 mM) were prepared from a dilute metal salt solution (c_M = 0.2 mM) by NaBH₄-induced reduction followed by ultracentrifugation. After the addition of oxidants (e.g., H₂O₂) or ethanol, NPs spontaneously fused and eventually formed a hydrogel after ~2 weeks. Finally, the corresponding free-standing MAs were obtained by supercritical CO₂ drying. However, the expensive ultracentrifugation process and long gelation time are not suitable for practical production.

Following the aforementioned study, the two-step strategy has been widely attempted. Apart from initiating gelation by adding oxidants and organic solvents, taking advantage of the salting-out effect, diverse salts (e.g., NaCl, CaCl₂, and NH₄F) were successfully used to efficiently induce the gelation process for Au, Ag, Pd, Pt, etc. [32,37,38,39]. In particular, by adjusting the ion–metal NPs interactions by applying specific salts, the proportion of the isotropic van der Waals attraction force and the anisotropic electrostatic repulsion force could be manipulated, thus leading to Au aerogels with modulated ligament sizes ranging from 6.9 to 113.7 nm [38]. Interestingly, a study reported by Wen et al. found that non-dissociative dopamine can serve as an efficient initiator, capable of producing Au aerogels with a ligament size of as small as ~5 nm and a SSA of up to 50.1 m² g⁻¹ [24]. However, the underlying gelation mechanism is not clear. In a follow-up study by the same group, with the assembly of D-penicillamine-stabilized ultrasmall Au nanoclusters (a diameter of 1.4 nm) with dopamine, the ligament size of the Au aerogels could be further cut down to ~3.5 nm [40]. Furthermore, controlled evaporation offers an initiator-free strategy for creating metal gels. As demonstrated by Jung et al., the aqueous suspension of as-prepared anisotropic 1D Ag NWs can be directly converted into a gel by gradual concentration via controlled evaporation at 313 K (Figure 1b), thus avoiding the introduction of extra impurities [31].

Considering that the NPs’ formation and assembly steps are decoupled in the two-step strategy, the NP precursors can be easily engineered before assembly, thus deriving MAs with controlled structures at both nano- and micro-scales [32,33,34,41,42,43,44,45]. Pioneered by Kulugammana and co-workers in 2013, as-prepared Au-Ag, Pd-Ag, and Pt-Ag alloy NSs were adopted for assembly [32]. As illustrated in Figure 1c, the obtained Au-Ag aerogel displays a hierarchical structure at different scales. In another interesting study, despite the fact that the same precursors (e.g., Ag NSs) were applied, the microstructure and thus the macroscopic transparency of the acquired aerogels could be substantially altered by controlling the etching degree by applying different amounts of C(NO₂)₄ (Figure 1d,e) [33]. Concentrating on the Pt system, a study prepared Pt nanocubes and nanospheres in an organic phase before treating them with N₂H₄·H₂O [34], eventually yielding a hierarchically structured aerogel (Figure 1f). Taking Ni NPs as sacrificial templates, by performing galvanic replacement reaction (GRR) with Pd and/or Pt salts, various Ni-Pd_xPt_y nano-building blocks with hollow spheres or dendrite-like structures were created as precursors [44,45]. Assembling these specific nanostructures leads to the formation of diverse hierarchically structured multi-metallic aerogels. However, the aforementioned strategies usually require a tedious pre-synthesis step for specifically engineered NPs. Besides deliberately shaping NPs, a counterintuitive phenomenon was reported; that is, the spatial element distribution of the resulting bimetallic aerogels is closely dependent on the chemical composition of the NP precursors [46]. It was found that the assembly of Au NPs and Ag NPs, Au NPs and Pd NPs, and Pd NPs and Pt NPs resulted in gels with uniform element distribution, core–shell structure, and separate element domain structures, respectively. This might be attributed to the composition-specific atomic reorganization during the gelation process.

Despite the above achievements, the available morphologies are still limited. On this occasion, when the as-prepared metal gels are regarded as “precursors”, certain complex structures can be created after specific treatment. For example, by performing GRR on a pre-synthesized Ag hydrogel with Pt salts, the derived Pt-Ag bimetallic gel exhibits a unique nanotubular-structured network with thin NWs (~2.6 nm in diameter) as the secondary structure [47]. Another study reported a PdAu-Pt core–shell aerogel by sequential underpotential Cu deposition and GRR [25]. However, these methods often suffer from time-consuming and/or costly processes. Recently, a dynamic-shelling approach was developed by our group, where the semi-finished gel was used as a precursor [22,38,48]. During the fabrication of a bimetallic gel, the “second metal” source was added after the partial gelation of the “first metal”. In this way, the “second metal” will nucleate and grow on the half-formed network of the “first metal”, thus giving rise to core–shell-structured MAs without an additional post-treatment step. This approach may point out a new direction on facile crafting complex structures in MAs.

Although the two-step strategy is advantageous in shaping multiscale structures, it often suffers from high costs and tedious operation. Therefore, the one-step strategy offers a feasible solution. In 2013, a one-step strategy was proposed by Liu and co-workers [35]. Briefly, Pd, Pt, and Pt-Pd gels were obtained from dilute metal salt aqueous solutions after 3–17 days by applying 1.5 equivalents of NaBH₄ (Figure 1g). This strategy merges the metal NP formation and the gelation into one step by only applying appropriate reductants, thus considerably simplifying the operation and reducing contamination. Obviously, the core of the one-step strategy lies in the rational selection of the type and the amount of reductants and also provides a comprehensive understanding of the roles played by the reductants in specific scenarios.

Following the first study on the NaBH₄-directed one-step method as described above, an array of reductants, including hydrazine, dimethylamine borane, sodium hypophosphite monohydrate, borane ammonia complex, and glyoxylic acid, were attempted, resulting in MAs based on Au, Ag, Pd, Pt, and Cu [23,36,49,50,51,52,53,54,55]. Among them, an interesting study found that a common organic solvent, i.e., N-methyl pyrrolidone, can function as both a reductant and a nitrogen source during a hydrothermal reaction [55]. The resulting Pt-Cu aerogels feature b oth a porous structure and unique metal–N bonds. Another study took gas-phase CO as a reductant, where Pd gels structured from 2D Pd nanosheets (thickness of 6.89 nm) were obtained from an acetic acid solution (Figure 1h) [36]. It is claimed that CO can not only reduce the Pd salts, but also serves as a ligand to promote the generation of the Pd nanosheets.

Very recently, our group systematically investigated the roles of NaBH₄—the most widely used reductant—in the gelation process [23]. It was found that the functions of NaBH₄ depend on the ratio of NaBH₄ to metal (R/M). At a low R/M (<2), all reductants are used for reducing the metal salts, resulting in metal aggregates. A moderate R/M (2–50) leads to a stable metal sol, at which the anions of the products and unreacted reductants can stabilize the as-formed metal NPs. A high R/M (>50) activates the salting-out function of NaBH₄, causing the formation of metal gels. In particular, an excessive amount of NaBH₄ can substantially promote the gelation process, where a short gelation time of several hours can be realized (vs. several days by other initiating approaches under similar conditions). Furthermore, the high efficiency of NaBH₄ allows the application of various ligands (e.g., trisodium citrate, sodium deoxycholate, β-alanine, and polyvinylpyrrolidone (PVP) for manipulating the behavior of the NP growth, enabling the fabrication of Au aerogels with a small ligament size (~4.8 nm) and a large SSA (59.8 m² g⁻¹). Meanwhile, single-metallic Ru, Rh, and Os aerogels were also obtained for the first time in the same study. Hence, deep analysis and subtly utilizing the multifunction of reactants (e.g., reductants, initiators, and solvents) are critical for a smart design of MAs.

For both one-step and two-step strategies, conventional studies mostly focus on modulating the reactants. However, it needs to be pointed out that smartly modulating external physical fields may offer a new dimension for controlled synthesis.

From the perspective of modulating the temperature field, an elevated temperature is frequently applied to accelerate the gelation process [51,56,57,58]. The first study was reported in 2013, where a substantially shortened gelation time was observed for the Au-Ag system from 2–3 weeks at room temperature (298 K) to 12 h at 348 K [56]. By performing gelation at 333 K, Shi et al. reported the quick synthesis of AuPt_x metal hydrogels within 2–4 h (Figure 2a) [57]. Meanwhile, the low-temperature field has also been studied, which can induce gelation and/or shape hierarchical structures [59,60,61,62,63,64,65,66,67,68]. For example, by setting a temperature gradient (from 223 K to 263 K) to promote the unidirectional growth of ice crystals, Ag NW aerogels with anisotropic structures and tunable pore sizes were obtained from an Ag NW precursor solution [62]. Starting from highly concentrated metal NP colloids (c_M > 100 mM), monolithic aerogels (Au, Ag, Pd, and Pt) consisting of self-supported networks can be obtained by freeze-casting (Figure 2b). However, ligands are required to stabilize this high-concentration precursor solution, resulting in residual impurities in the product [63]. To overcome the aforementioned issues, a freeze–thaw method was developed by our group, capable of building hierarchically structured noble-metal gels (e.g., Au, Pd, Rh, Au-Pt, and Au-Rh) directly from low-concentration NP solutions (c_M ≤ 0.5 mM) [67]. As shown in Figure 2c, metal NPs form aggregates (or gel pieces) upon freezing. Then, due to their self-healing property, these aggregates precipitate and link together during the following thawing process, eventually yielding a monolithic gel. In particular, the ligament size of the resulting Au aerogel is as small as (35.0 ± 7.2) nm, which is about one order of magnitude thinner than that of the freeze-casting-prepared one (200–500 nm).

Furthermore, the influence of external force fields on aerogel synthesis has been studied. To meet practical production times, it is critical to accelerate the slow gelation process in metal systems (several hours to several weeks). To address this issue, our group proposed an unconventional disturbance-directed gelation strategy to accelerate the mass transfer [22,48]. Inspired by the self-healing properties of metal hydrogels, a shearing field generated by stirring was introduced for promoting the mass transfer. After the formation of Au aggregates, the reaction system was left still for gelation via self-healing of the as-formed aggregates (Figure 2d). In this light, the gelation time can be reduced to 1–10 min, which is 2–4 orders of magnitude faster than that reported by conventional methods. It needs to be mentioned that the nature of the self-healing properties of metal hydrogels has not been well understood. Additionally, the feasibility of expansion of such disturbance-directed synthesis tactics to more gel systems should be a meaningful while under-investigated direction.

3. Fuel-Related Electrocatalysis

3.1. Alcohol Oxidation Reaction

Direct alcohol fuel cells, which are fueled by alcohols (e.g., methanol and ethanol), have drawn increasing attention due to their high energy efficiency and low pollution emissions compared with fossil fuels [69]. However, the anodic alcohol oxidation reaction (AOR) is hindered by a high overpotential (η) and sluggish kinetics compared to hydrogen oxidation, thus calling for a new generation of electrocatalysts [70,71]. In this regard, MAs play a critical role due to their excellent performance in the electrocatalytic oxidation of diverse alcohols, including methanol, ethanol, and ethylene glycol. In practice, the design of MAs for AOR can roughly be divided into composition and structure aspects.

Composition design is mostly performed by imparting specific metals or tuning the proportions of different metals, so as to enhance the electrical conductivity and/or modulate the electronic structure [38,44,51,57,58,72,73,74,75]. In most studies, Pd- and Pt-based aerogels are employed for AOR catalysis due to the intrinsically high activity of Pd and Pt. In an early study, α-, β-, or γ-cyclodextrins-modified Pd aerogels were applied for the ethanol oxidation reaction (EOR) [74]. The corresponding forward anodic peak current densities (I_f) normalized by the Pd mass (4.12 to 7.39 A mg⁻¹) are larger than that of commercial Pd/C (3.43 A mg⁻¹), showcasing a higher catalytic activity. The ratios of the peak current densities obtained from forward/backward scans (I_f/I_b) of those aerogels are 1.06 to 1.17 times higher than that of commercial Pd/C, suggesting more efficient oxidation during the forward anodic scan. The high electrocatalytic activity is considered to be the abundant active sites and mass transfer channels of the aerogel, as well as the host–guest interaction between the cyclodextrins and ethanol. Then, a batch of studies were dedicated to enhancing the performance by using bi-/tri-MAs. For instance, by introducing Au and Pt, the resulting Au-Pd and Au-Pd-Pt aerogels exhibit substantially higher performance with I_f of 2.65 and 4.82 A mg_{Pd + Pt}⁻¹, respectively (2.8 to 6.1 times higher than that for commercial Pd/C) [38]. This is rationalized by highly conductive 3D networks offered by gold and potential synergy effects from several metals. Furthermore, considering the cost, inexpensive Cu has also been included [58]. As seen from Figure 3a,b, the Pd₆₈Cu₃₂ aerogel delivers a high forward current density of 3.47 A mg_Pd⁻¹ in 1.0 M KOH + 1.0 M ethanol solution, presumably due to its large electrochemically active surface area (37.9 m² g⁻¹, higher than 13.8 m² g⁻¹ of Pd/C).

Apart from modulating the metal compositions, specific ligands were adopted to adjust the valence state of the aerogels by utilizing the electron charge transfer between the metals and ligands. As shown in Figure 3c,d, a partial electron transfer from the metal to PVP was observed, resulting in a higher surface oxidation state of Au-Pd aerogels and thus promoting the oxidation reaction [75]. In this light, an EOR activity 5.3 times higher than that for Pd/C was realized with the PVP-modified Au-Pd aerogel.

On the other hand, the manipulation of the aerogel structure has been explored at both the nanoscale and the meso-/macroscale to boost the electrocatalytic performance [36,43,44,52,54,67,76]. Bearing a unique core–shell structure at the nanoscale, a Pd₃Pb₁@Pd aerogel shows a high I_f of 6.4 A mg_Pd⁻¹ (5.8 times higher than that for Pd black) towards the ethylene glycol oxidation reaction in 1.0 M KOH + 0.5 M ethylene glycol [54]. In another study, Ni-PdPt aerogels with hollow-spherical and dendritic morphologies at the nanoscale were designed (Figure 3e) [44]. Thanks to the large numbers of accessible catalytic sites, the dendritically structured Ni-Pd₆₀Pt₄₀ aerogel manifests an impressive I_f of 10.6 times higher than with Pd/C (Figure 3f). At the meso-/macroscale, Au-Pd aerogels featuring hierarchically porous structures demonstrate unique advantages (Figure 3g) [67]. As illustrated in Figure 3h, a high I_f of 8.4 A mg⁻¹ was obtained due to a combination of enhanced mass transfer and abundant active sites.

In addition to conventional electrocatalysis, MAs have been recently explored as a photoelectrocatalysis (PEC) platform by utilizing the combined optic and catalytic activities endowed by nanostructured metals. This endeavor was pioneered in 2020 by our group, where the photocatalytic performance for EOR was evaluated with an Au-Pd-Pt aerogel under a white-light LED source (wavelength range of 350–800 nm) (Figure 4a) [22]. As seen from Figure 4b, I_f of the Au-Pd-Pt aerogel raises stepwise from 9.1 to 13.2 A mg_Pd+Pt⁻¹ as the light power density increases from 0 to 133 mW cm⁻², which are 5.0 to 7.3 times higher than that of commercial Pd/C in the dark. This light-enhanced performance may be attributed to both the plasmonic absorption of nanostructured noble metals, as well as the photothermal effect from multiple light absorption/scattering inside the gel network. Interestingly, this property may also find applications in sensing. As shown in Figure 4c, switching on/off the light during a chronoamperometry test results in repeated current fluctuations, manifesting a sensitivity of >40.2 μA mW⁻¹. A follow-up study explored PEC for EOR by using hierarchically structured Au-Pd and Au-Pt aerogels (Figure 4d–f) [67]. Similarly, a ~40% improvement in I_f was observed with an Au-Pd aerogel under irradiation compared with that in the dark (11.8 vs. 8.4 A mg⁻¹), both considerably outperforming that for commercial Pd/C (1.8 A mg⁻¹ in the dark).

3.2. Formic Acid/Formate Oxidation Reaction

FOR has also drawn substantial interest in recent years on account of the high energy density and security of formic acid/formate [77]. MAs have also been applied for electrocatalyzing FOR [47,50,78,79,80,81]. In 2018, a Pd-Cu aerogel was reported for efficiently catalyzing formic acid oxidation [50]. In a 0.5 M H₂SO₄ and 0.5 M HCOOH solution, the Pd-Cu aerogel displayed a high current density of 3.13 A mg_Pd⁻¹, which nearly doubled that of Pd/C (1.67 A mg_Pd⁻¹). This improved performance can be attributed to the self-supported nature of aerogels, which eliminates the potential carbon substrate corrosion that happens in commercial Pd/C. Recently, an in situ high-potential-driven restructuring strategy was proposed to promote electrocatalytic HCOOK oxidation in alkaline media [80]. As schemed in Figure 5a, the potential cycling of a ternary Ag-Pd-Pt aerogel leads to an outward diffusion of Ag and thus generates amorphous Ag₂O-coupled Pd-Pt on the surface. This architecture can weaken the chemisorption of H_ad intermediate because of the lowered d-band center, thus promoting FOR. By cycling Ag-Pd-Pt aerogels between 0.1 V and 1.3 V, the resulting materials exhibit outstanding activity (5 times higher than that for Pd/C) and stability (Figure 5b).

3.3. Glucose and Borohydride Oxidation Reaction

Glucose is a long-sought-after renewable fuel that can largely advance green energy technologies, and MAs play a critical role in catalyzing the glucose oxidation reaction (GOR) [24,37,40,82]. On the one hand, MAs can act as an auxiliary component to promote the GOR. For example, a Pd aerogel was used as a porous and electrically conductive host to load catalytically active glucose oxidase (GOD) [37]. In this way, mass/electron transfer was enhanced, thus considerably raising the bioelectrocatalytic current compared to that for a bare GOD electrode. On the other hand, MAs can also directly catalyze GOR [24]. As seen in Figure 5c, the current density increases linearly with increasing concentration of glucose from 0 to 20 mM. Particularly, the β-CD-modified Au aerogel displays the highest sensitivity of (332.9 ± 7.6) μA mM⁻¹, which might be attributed to the intermolecular interaction between glucose and β-CD.

Besides the GOR, the borohydride oxidation reaction (BOR) has also been studied recently [73]. As seen from Figure 5d,e, Au-Cu aerogels manifest composition-dependent BOR performance. Among them, the Au₅₂Cu₄₈ aerogel features the most negative onset potential and the highest current density (53 mA cm⁻²), which is believed to originate from its desirable electronic structure that can excellently balance the borohydride adsorption and intermediate desorption.

4. Oxygen-Related Electrocatalysis

OER and ORR are two oxygen-related electrocatalytic reactions, which are important in the field of energy conversion and storage [83,84,85,86]. OER is found as the anodic reaction in water electrolysis, while its large η (usually >300 mV) seriously affects this process [5]. On the other hand, as the cathode reaction in fuel cells and metal-air batteries, ORR is the bottleneck reaction because of its sluggish four-electron transfer process [2]. Commercial OER and ORR catalysts are usually noble-metal-based materials (e.g., Ir- and Ru-based catalysts for OER and Pt-based catalysts for ORR), while their high cost can pose a large constraint for upscaled use. In this regard, MAs may offer unprecedented opportunities by considerably increasing the performance-to-cost ratio for their extended reaction sites and mass transfer highways.

4.1. Oxygen Evolution Reaction

Diverse MAs have been applied for OER catalysis [23,87,88,89]. As seen in Figure 6a,b, based on the synergy of the highly conductive Au core network and the catalytically active Ir shell, Au-Ir core–shell aerogels manifest a small η (245 mV at 10 mA cm⁻²) and Tafel slope (36.9 mV dec⁻¹) in 1.0 M KOH, considerably outperforming commercial Ir/C and IrO₂ catalysts (η > 311 mV and Tafel slope > 54.3 mV dec⁻¹) [23].

To reduce the cost, non-noble metals are introduced into MAs in recent studies. For instance, Ru-Co aerogels were found with high electrical conductivity, as well as abundant active sites, resulting from the presence of oxygen vacancies, thus delivering a small OER η (272 mV at 10 mA cm⁻²) and Tafel slope (41.6 mV dec⁻¹) in 1.0 M KOH [87]. Another study reported nanovoids-incorporated Ir_xCu aerogels for enhanced OER performance (Figure 6c) [88]. By balancing the binding energy of the oxygen-involved intermediates and the desorption energy of the generated oxygen via tuning the composition, the optimized Ir₃Cu aerogel exhibits the smallest η (298 mV at 10 mA cm⁻²) in an O₂-saturated 0.1 M HClO₄ aqueous solution (Figure 6d). Recently, a noble-metal-free Fe-Co-Ni aerogel, as a cost-effective OER electrocatalyst, was found to deliver an exceptionally low η (235 mV at 10 mA cm⁻²) and a small Tafel slope (50 mV dec⁻¹) in 1.0 M KOH, outperforming that for commercial RuO₂ and thereby offering opportunities towards commercial use [89]. The enhanced performance is due to the synergistic effect of three metals as well as abundant catalytically active structural defects found in the aerogel.

4.2. Oxygen Reduction Reaction

MAs have also been used for catalyzing ORR in recent years, particularly with Pt-based aerogels [35,39,90,91]. The first study was reported in 2013 with Pd-Pt bimetallic aerogels [35]. By tuning the d-band center of the aerogels via modulating the Pd-to-Pt ratio, the optimized Pd₂₀Pt₈₀ aerogel exhibits a 5-times-higher mass activity (1.17 A mg_Pt+Pd⁻¹) than that for commercial Pt/C (0.23 A mg_Pt⁻¹). By introducing highly conductive Au to enhance the electron transfer, the acquired Au-Pt aerogel delivers an impressive pH-universal ORR catalytic performance, exhibiting a high specific activity (>3 times compared with that for Pt/C) and stability in both 0.1 M KOH and 0.1 M HClO₄ aqueous solutions [39]. Inspired by the outstanding ORR catalytic performance of Pt-Ni nanostructures [92], Pt-Ni aerogels were fabricated as cathode catalysts for fuel cells, showcasing both excellent specific activity (0.2 mA cm_Pt⁻² at 0.95 V_RHE under acidic conditions, which is 3 times higher than that for Pt/C) and stability (~10% decrease in mass activity at 0.9 V_RHE after 10000 potential cycles) [90,91]. Furthermore, Pt-free MAs, such as Au-Cu aerogels, were also investigated [73]. As seen from Figure 6e,f, the charge transfer from Cu to Au can lower the d-band center of Au, thus the resulting in the Au₅₂Cu₄₈ aerogel displaying a more positive onset potential compared with commercial Pt/C (1.00 V and 0.96 V vs. RHE, respectively) and sustaining high specific activity (0.891 mA cm⁻²) and mass activity (0.920 A mg_Au⁻¹) after 10,000 potential cycles. This is presumably associated with the superior stability provided by the Au component.

On the other hand, structure engineering of MAs can also enhance the ORR performance. For example, taking advantage of the synergy of the highly conductive Au core network and the Pt₃Pd shell, a specially designed Au@Pt₃Pd core–shell aerogel was shown to deliver much higher mass activity and specific activity (0.812 A mg_Pt+Pd⁻¹ and 24.3 mA cm⁻²) than that for commercial Pt/C (0.412 A mg_Pt⁻¹ and 10.5 mA cm⁻²) at 0.85 V vs. RHE [42]. Core-shell-structured Pd_xAu-Pt aerogels, consisting of an ultrathin Pt shell and a composition-tunable Pd_xAu core, were also explored as electrocatalysts [25]. By manipulating the lattice strain through designing the lattice mismatch between the outer Pt and various core metals, the optimized PdAu-Pt core–shell aerogel exhibits incredible mass activity and specific activity of 5.25 A mg_Pt⁻¹ and 2.53 mA cm⁻², which are 18.7- and 4.1 times higher than those of Pt/C (Figure 6g,h).

5. Hydrogen-Related Electrocatalysis

Electrocatalysis with hydrogen can be divided into two classes, i.e., the hydrogen oxidation reaction and the hydrogen evolution reaction. The eco-friendly HOR process acts as the anodic reaction in hydrogen fuel cells, while the HER process is the cathodic reaction in the electrochemical water splitting that is critical for hydrogen production.

5.1. Hydrogen Oxidation Reactions

So far, electrocatalytic HOR has been only sporadically studied with MAs. As seen from Figure 7a, 2D lamellar Pt-Rh nanoalloy aerogels (NAAs) made up of ultrathin interweaved NWs were reported [93]. The authors claimed that strong electronic coupling between Pt and Rh can weaken the hydrogen binding energy (Figure 7b), thus leading to a lower half-wave potential (E_1/2) of 17 mV, as well as the highest specific activity and mass activity (5.5 and 2.6 times higher than that of commercial Pt/C, respectively, at η = 50 mV) among all tested catalysts (Figure 7c,d).

5.2. Hydrogen Evolution Reactions

Recently, MAs were also extensively studied for HER [39,93,94,95]. In terms of the structure, besides HOR catalysis, 2D-sheets-assembled Pt-Rh NAAs also perform well towards alkaline HER, exhibiting a smaller η of 55 mV at 10 mA cm⁻², as well as a 2.3-times-higher mass activity in 1.0 M KOH solution compared to Pt/C [93]. In another study, by grafting two kinds of ligands (L1 and L2) bearing thiol and glutamic acid moieties on Pt NWs for controlled assembly, the resulting aerogels displayed different HER performances [94]. The strong self-assembling ability of L2 renders the Pt_NW-L2 aerogels (Figure 7e) with an optimized performance (the lowest η of 45 mV at 10 mA cm⁻²) among the tested materials (Figure 7f), but the specific reason is unclear. On the other hand, the smart design of the composition also plays a critical role. By screening various bimetallic systems, Au-Rh aerogels were found to deliver the smallest η (18–22 mV at 10 mA cm⁻²) and Tafel slopes (29–47 mV) at different pH values (pH = 0–14), considerably outperforming commercial Pt/C catalysts [39]. However, a clear explanation is absent.

6. Electrocatalysis in Other Processes

Apart from the above examples, MAs have also been involved in various other important electrocatalytic processes, such as the CO₂ reduction reaction (CO₂RR) and the nitrate reduction reaction.

Electrochemical CO₂RR provides a promising way of meeting current energy demands and reducing greenhouse gas emissions by producing value-added chemicals with renewable electricity. MAs also play a critical role in this field [48,96,97,98,99]. Lu et al. reported the first study on CO₂RR with Mas [97]. By regulating the composition of bimetallic Pd-Cu aerogels, the Pd₈₃Cu₁₇ aerogel with the highest (Cu^I + Cu⁰)/Cu^II ratio displayed the best performance, with a faradaic efficiency of 80.0% at a current density of 31.8 mA cm⁻² for CH₃OH production in 1-butyl-3-methylimidazolium tetrafluoroborate aqueous solution. The excellent performance is rationalized by the efficient adsorption of CO_ads and CHO_ads on Cu^I + Cu⁰ species. From the structure aspect, a well-defined Au-Pd core–shell aerogel (Figure 8a) was found to efficiently promote CO₂ activation while suppressing H₂ activation evolution compared to common Au-Pd aerogels as suggested by both experimental and theoretical studies (Figure 8b,c), thus manifesting outstanding Faradaic efficiency of up to 99.96% for CO selectivity and sustaining a FE_CO > 98% at η = 390 mV over 12 h [48].

Besides CO₂ conversion, a growing level of nitrate (NO³⁻) places another potential threat to the environment. To address it, Cu-rich Cu-Pd bimetallic aerogels were developed by choosing Pd as the active metal and Cu as the promoting metal [100]. Among all tested catalysts (Figure 8d,e), the Cu-Pd (3:1) aerogel stands out for the enhanced hydrogen adsorption at Pd-sites and the well-tuned d-band center of Cu. In this light, a high NO³⁻ conversion rate (95.27%), ammonia selectivity (77.49%), and ammonia faradaic efficiency (90.02%) at 0.46 V vs. RHE were acquired. The superior performance could be attributed to the abundant catalytically active sites provided by the aerogel structure as well as the synergy of Cu and Pd.

7. Conclusions and Perspectives

The last decade witnessed the discovery and prosperous development of MAs as well as their widespread applications in electrocatalysis. As one of the latest members in the aerogel family, MAs have proved highly desirable for diverse applications, including catalysis, optical devices, and sensing. Meanwhile, the uniqueness of MAs also brings about quite a few challenges.

Fundamentally, the distinctive properties of metals (e.g., high mass density, plasticity, and delocalized electrons) lead to abnormal gelation behavior compared to conventional gel systems. Despite tremendous efforts devoted, a general and unambiguous understanding of the physical picture of the gelation process is still absent, thus restricting investigations of controlled synthesis as well as properties. For the following five or more years, it is expected that the development of the synthesis methodology, the enrichment of the material basis, and the exploration of basic physicochemical properties of MAs are sought-after directions in this field.

Practically, it is accepted that the most promising application of MAs at present is electrocatalysis based on the combined effects of a highly conductive network, large SSA, and abundant active sites. Principles for performance optimization can be summarized into composition tuning (for enhancing the conductivity and adjusting the electronic structure) and structure tuning (for increasing accessible sites). Currently, most studies concentrate on noble metal systems, which inevitably raises the cost. Additionally, quite a few studies only superficially demonstrate catalytic performance without investigating underlying mechanisms, which contributes little to the development of practical applications. Thirdly, the aerogel form seems useless under the conventional catalyst preparation process (grinding and dispersing). The subtle utilization of the free-standing feature of MAs needs to be considered when applied for electrocatalysis and beyond. Finally, the unique features of metals are still less explored. Our group has pioneered photoelectrocatalysis with MAs by taking advantage of their optical properties, while more attributes of metals and MAs are waiting to be discovered.

To sum up, as a class of cutting-edge materials, MAs deserve much more attention due to unsolved fundamental challenges and broad application perspectives. Researchers with multi-disciplinary backgrounds ranging from chemistry, materials science, physics, and biology are welcome to jointly explore this young and promising field.