FeS2 Nanoparticles Embedded in Reduced Graphene Oxide toward Robust,High‐Performance Electrocatalysts

Developing low‐cost, highly efficient, and robust earth‐abundant electrocatalysts for hydrogen evolution reaction (HER) is critical for the scalable production of clean and sustainable hydrogen fuel through electrochemical water splitting. This study presents a facile approach for the synthesis of nanostructured pyrite‐phase transition metal dichalcogenides as highly active, earth‐abundant catalysts in electrochemical hydrogen production. Iron disulfide (FeS₂) nanoparticles are in situ loaded and stabilized on reduced graphene oxide (RGO) through a current‐induced high‐temperature rapid thermal shock (≈12 ms) of crushed iron pyrite powder. FeS₂ nanoparticles embedded in between RGO exhibit remarkably improved electrocatalytic performance for HER, achieving 10 mA cm^?2 current at an overpotential as low as 139 mV versus a reversible hydrogen electrode with outstanding long‐term stability under acidic conditions. The presented strategy for the design and synthesis of highly active earth‐abundant nanomaterial catalysts paves the way for low‐cost and large‐scale electrochemical energy applications.     

Eutectic‐Derived Mesoporous Ni‐Fe‐O Nanowire Network Catalyzing Oxygen Evolution and Overall Water Splitting

The development of efficient and abundant water oxidation catalysts is essential for the large‐scale storage of renewable energy in the form of hydrogen fuel via electrolytic water splitting, but still remains challenging. Based upon eutectic reaction and dealloying inheritance effect, herein, novel Ni‐Fe‐O‐based composite with a unique mesoporous nanowire network structure is designed and synthesized. The composite exhibits exceptionally low overpotential (10 mA cm^?2 at an overpotential of 244 mV), low Tafel slope (39 mV dec^?1), and superior long‐term stability (remains 10 mA cm^?2 for over 60 h without degradation) toward oxygen evolution reaction (OER) in 1 m KOH. Moreover, an alkaline water electrolyzer is constructed with the Ni‐Fe‐O composite as catalyst for both anode and cathode. This electrolyzer displays superior electrolysis performance (affording 10 mA cm^?2 at 1.64 V) and long‐term durability. The remarkable features of the catalyst lie in its unique mesoporous nanowire network architecture and the synergistic effect of the metal core and the active metal oxide, giving rise to the strikingly enhanced active surface area, accelerated electron/ion transport, and further promoted reaction kinetics of OER.     

Bi‐Functional Iron‐Only Electrodes for Efficient Water Splitting with Enhanced Stability through In Situ Electrochemical Regeneration

Scalable and robust electrocatalysts are required for the implementation of water splitting technologies as a globally applicable means of producing affordable renewable hydrogen. It is demonstrated that iron‐only electrode materials prove to be active for catalyzing both proton reduction and water oxidation in alkaline electrolyte solution with superior activity to that of previously established bi‐functional catalysts containing less abundant elements. The reported bi‐functionality of the iron electrodes is reversible upon switching of the applied bias through electrochemical interconversion of catalytic species at the electrode surface. Cycling of the applied bias results in in‐situ electrochemical regeneration of the catalytic surfaces and thereby extends the catalyst stability and lifetime of the water electrolyzer. Full water splitting at a current density of I = 10 mA cm^?2 is achieved at a bias of ≈2 V, which is stable over at least 3 d (72 one hour switching cycles). Thus, potential‐switching is established as a possible strategy of stabilizing electrode materials against degradation in symmetrical water splitting systems.     

Ultrafine Pt Nanoparticle‐Decorated Pyrite‐Type CoS2 Nanosheet Arrays Coated on Carbon Cloth as a Bifunctional Electrode for Overall Water Splitting

To improve the utilization efficiency of precious metals, metal‐supported materials provide a direction for fabricating highly active and stable heterogeneous catalysts. Herein, carbon cloth (CC)‐supported Earth‐abundant CoS₂ nanosheet arrays (CoS₂/CC) are presented as ideal substrates for ultrafine Pt deposition (Pt‐CoS₂/CC) to achieve remarkable performance toward the hydrogen and oxygen evolution reactions (HER/OER) in alkaline solutions. Notably, the Pt‐CoS₂/CC hybrid delivers an overpotential of 24 mV at 10 mA cm^?2 and a mass activity of 3.89 A Pt_mg^?1, which is 4.7 times higher than that of commercial Pt/C, at an overpotential of 130 mV for catalyzing the HER. An alkali‐electrolyzer using Pt‐CoS₂/CC as a bifunctional electrode enables a water‐splitting current density of 10 mA cm^?2 at a low voltage of 1.55 V and can sustain for more than 20 h, which is superior to that of the state‐of‐the‐art Pt/C+RuO₂ catalyst. Further experimental and theoretical simulation studies demonstrate that strong electronic interaction between Pt and CoS₂ synergistically optimize hydrogen adsorption/desorption behaviors and facilitate the in situ generation of OER active species, enhancing the overall water‐splitting performance. This work highlights the regulation of interfacial and electronic synergy in pursuit of highly efficient and durable supported catalysts for hydrogen and oxygen electrocatalytic applications.     

A Perovskite Nanorod as Bifunctional Electrocatalyst for Overall Water Splitting

The development of highly efficient and low‐cost electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is paramount for water splitting associated with the storage of clean and renewable energy. Here, this study reports its findings in the development of a nanostructured perovskite oxide as OER/HER bifunctional electrocatalyst for overall water splitting. Prepared by a facile electrospinning method, SrNb_0.1Co_0.7Fe_0.2O_3–δ perovskite nanorods (SNCF‐NRs) display excellent OER and HER activity and stability in an alkaline solution, benefiting from the catalytic nature of perovskites and unique structural features. More importantly, the SNCF‐NR delivers a current density of 10 mA cm^?2 at a cell voltage of merely ≈1.68 V while maintaining remarkable durability when used as both anodic and cathodic catalysts in an alkaline water electrolyzer. The performance of this bifunctional perovskite material is among the best ever reported for overall water splitting, offering a cost‐effective alternative to noble metal based electrocatalysts.     

Ni Strongly Coupled with Mo2C Encapsulated in Nitrogen‐Doped Carbon Nanofibers as Robust Bifunctional Catalyst for Overall Water Splitting

It is urgently required to develop highly efficient and stable bifunctional non‐noble metal electrocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) for water splitting. In this study, a facile electrospinning followed by a post‐carbonization treatment to synthesize nitrogen‐doped carbon nanofibers (NCNFs) integrated with Ni and Mo₂C nanoparticles (Ni/Mo₂C‐NCNFs) as water splitting electrocatalysts is developed. Owing to the strong hydrogen binding energy on Mo₂C and high electrical conductivity of Ni, synergetic effect between Ni and Mo₂C nanoparticles significantly promote both HER and OER activities. The optimized hybrid (Ni/Mo₂C(1:2)‐NCNFs) delivers low overpotentials of 143 mV for HER and 288 mV for OER at a current density of 10 mA cm^?2. An alkaline electrolyzer with Ni/Mo₂C(1:2)‐NCNFs as catalysts for both anode and cathode exhibits a current density of 10 mA cm^?2 at a voltage of 1.64 V, which is only 0.07 V larger than the benchmark of Pt/C‐RuO₂ electrodes. In addition, an outstanding long‐term durability during 100 h testing without obvious degradation is achieved, which is superior to most of the noble‐metal‐free electrocatalysts reported to date. This work provides a simple and effective approach for the preparation of low‐cost and high‐performance bifunctional electrocatalysts for efficient overall water splitting.     

Polydopamine‐Inspired,Dual Heteroatom‐Doped Carbon Nanotubes for Highly Efficient Overall Water Splitting

Overall water splitting involved hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are critical for renewable energy conversion and storage. Heteroatom‐doped carbon materials have been extensively employed as efficient electrocatalysts for independent HER or OER processes, while those as the bifunctional catalysts for simultaneously generating H₂ and O₂ by splitting water have been seldom reported. Inspired by the unparalleled virtues of polydopamine, the authors devise the facile synthesis of nitrogen and sulfur dual‐doped carbon nanotubes with in situ, homogenous and high concentration sulfur doping. The newly developed dual‐doped electrocatalysts display superb bifunctional catalytic activities for both HER and OER in alkaline solutions, outperforming all other reported carbon counterparts. Experimental characterizations confirm that the excellent performance is attributed to the multiple doping together with efficient mass and charge transfer, while theoretical computations reveal the promotion effect of secondary sulfur dopant to enhance the spin density of dual‐doped samples and consequently to form highly electroactive sites for both HER and OER.     

Earth‐Abundant Iron Diboride (FeB2) Nanoparticles as Highly Active Bifunctional Electrocatalysts for Overall Water Splitting

Developing efficient, durable, and earth‐abundant electrocatalysts for both hydrogen and oxygen evolution reactions is important for realizing large‐scale water splitting. The authors report that FeB₂ nanoparticles, prepared by a facile chemical reduction of Fe²⁺ using LiBH₄ in an organic solvent, are a superb bifunctional electrocatalyst for overall water splitting. The FeB₂ electrode delivers a current density of 10 mA cm^?2 at overpotentials of 61 mV for hydrogen evolution reaction (HER) and 296 mV for oxygen evolution reaction (OER) in alkaline electrolyte with Tafel slopes of 87.5 and 52.4 mV dec^?1, respectively. The electrode can sustain the HER at an overpotential of 100 mV for 24 h and OER for 1000 cyclic voltammetry cycles with negligible degradation. Density function theory calculations demonstrate that the boron‐rich surface possesses appropriate binding energy for chemisorption and desorption of hydrogen‐containing intermediates, thus favoring the HER process. The excellent OER activity of FeB₂ is ascribed to the formation of a FeOOH/FeB₂ heterojunction during water oxidation. An alkaline electrolyzer is constructed using two identical FeB₂‐NF electrodes as both anode and cathode, which can achieve a current density of 10 mA cm^?2 at 1.57 V for overall water splitting with a faradaic efficiency of nearly 100%, rivalling the integrated state‐of‐the‐art Pt/C and RuO₂/C.     

Hybrid Photoelectrochemical Water Splitting Systems: From Interface Design to System Assembly

Photoelectrochemical (PEC) water splitting has attracted increasing attention due to its potential to mitigate energy and environmental issues. Hybrid PEC systems containing semiconductor photosensitizers and molecular catalysts are reported to be highly active and stable for water splitting with great potential for facilitating clean fuels production. In this review, following a showcasing of the fundamental details of hybrid PEC systems for water splitting, semiconductor/molecular catalyst interface designs are highlighted, with a focus on interfacial physicochemical interactions and binding, and interfacial energetics and dynamics for efficient charge transfer. Recent advances in hybrid system assemblies for PEC water splitting are also briefly introduced. Finally, future challenges and directions in the field of hybrid PEC water splitting for solar energy conversion are reviewed. The current review provides state‐of‐the‐art strategies for optimized interface design for creating highly active and stable PEC water splitting assemblies.     

Atomically Dispersed Mo Supported on Metallic Co9S8 Nanoflakes as an Advanced Noble‐Metal‐Free Bifunctional Water Splitting Catalyst Working in Universal pH Conditions

Water splitting requires development of cost‐effective multifunctional materials that can catalyze both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) efficiently. Currently, the OER relies on the noble‐metal catalysts; since with other catalysts, its operation environment is greatly limited in alkaline conditions. Herein, an advanced water oxidation catalyst based on metallic Co₉S₈ decorated with single‐atomic Mo (0.99 wt%) is synthesized (Mo‐Co₉S₈@C). It exhibits pronounced water oxidization activity in acid, alkali, and neutral media by showing positive onset potentials of 200, 90, and 290 mV, respectively, which manifests the best Co₉S₈‐based single‐atom Mo catalyst till now. Moreover, it also demonstrates excellent HER performance over a wide pH range. Consequently, the catalyst even outperforms noble metal Pt/IrO₂‐based catalysts for overall water splitting (only requiring 1.68 V in acid, and 1.56 V in alkaline). Impressively, it works under a current density of 10 mA cm^?2 with no obvious decay during a 24 h (0.5 m H₂SO₄) and 72 h (1.0 m KOH) durability experiment. Density functional theory (DFT) simulations reveal that the synergistic effects of atomically dispersed Mo with Co‐containing substrates can efficiently alter the binding energies of adsorbed intermediate species and decrease the overpotentials of the water splitting.     

Solar‐to‐Hydrogen Energy Conversion Based on Water Splitting

Artificial photosynthesis provides a blueprint to harvest solar energy to sustain the future energy demands. Solar‐driven water splitting, converting solar energy into hydrogen energy, is the prototype of photosynthesis. Various systems have been designed and evaluated to understand the reaction pathways and/or to meet the requirements of potential applications. In solar‐to‐hydrogen conversion, electrocatalytic hydrogen and oxygen evolution reactions are key research areas that are meaningful both theoretically and practically. To utilize hydrogen energy, fuel cell technology has been extensively investigated because of its high efficiency in releasing chemical energy. In this review, general concepts of the photosynthesis in green plants are discussed, different strategies for the light‐driven water splitting proposed in laboratories are introduced, the progress of electrocatalytic hydrogen and oxygen evolution reactions are reviewed, and finally, the reactions in hydrogen fuel cells are briefly discussed. Overall, the mass and energy circulation in the solar‐hydrogen‐electricity circle are delineated. The authors conclude that attention from scientists and engineers of relevant research areas is still highly needed to eliminate the wide disparity between the aspirations and realities of artificial photosynthesis.     

Ultralow Ru Loading Transition Metal Phosphides as High‐Efficient Bifunctional Electrocatalyst for a Solar‐to‐Hydrogen Generation System

Water splitting is a promising technology for sustainable conversion of hydrogen energy. The rational design of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) bifunctional electrocatalysts with superior activity and stability in the same electrolyte is the key to promoting their large‐scale applications. Herein, an ultralow Ru (1.08 wt%) transition metal phosphide on nickel foam (Ru–MnFeP/NF) derived from Prussian blue analogue, that effectively drivies both the OER and the HER in 1 m KOH, is reported. To reach 20 mA cm^?2 for OER and 10 mA cm^?2 for HER, the Ru–MnFeP/NF electrode only requires overpotentials of 191 and 35 mV, respectively. Such high electrocatalytic activity exceeds most transition metal phosphides for the OER and the HER, and even reaches Pt‐like HER electrocatalytic levels. Accordingly, it significantly accelerates full water splitting at 10 mA cm^?2 with 1.470 V, which outperforms that of the integrated RuO₂ and Pt/C couple electrode (1.560 V). In addition, the extremely long operational stability (50 h) and the successful demonstration of a solar‐to‐hydrogen generation system through full water splitting provide more flexibility for large‐scale applications of Ru–MnFeP/NF catalysts.     

Enabling Iron‐Based Highly Effective Electrochemical Water‐Splitting and Selective Oxygenation of Organic Substrates through In Situ Surface Modification of Intermetallic Iron Stannide Precatalyst

A strategy to overcome the unsatisfying catalytic performance and the durability of monometallic iron‐based materials for the electrochemical oxygen evolution reaction (OER) is provided by heterobimetallic iron–metal systems. Monometallic Fe catalysts show limited performance mostly due to poor conductivity and stability. Here, by taking advantage of the structurally ordered and highly conducting FeSn₂ nanostructure, for the first time, an intermetallic iron material is employed as an efficient anode for the alkaline OER, overall water‐splitting, and also for selective oxygenation of organic substrates. The electrophoretically deposited FeSn₂ on nickel foam (NF) and fluorine‐doped tin oxide (FTO) electrodes displays remarkable OER activity and durability with substantially low overpotentials of 197 and 273 mV at 10 mA cm^?2, respectively, which outperform most of the benchmarking NiFe‐based catalysts. The resulting superior activity is attributed to the in situ generation of α‐FeO(OH)@FeSn₂ where α‐FeO(OH) acts as the active site while FeSn₂ remains the conductive core. When the FeSn₂ anode is coupled with a Pt cathode for overall alkaline water‐splitting, a reduced cell potential (1.53 V) is attained outperforming that of noble metal‐based catalysts. FeSn₂ is further applied as an anode to produce value‐added products through selective oxygenation reactions of organic substrates.     

All‐In‐One Perovskite Catalyst: Smart Controls of Architecture and Composition toward Enhanced Oxygen/Hydrogen Evolution Reactions

A conventional water electrolyzer consists of two electrodes, each of which is embedded with a costly and rare electrocatalyst, typically IrO₂/C for oxygen evolution reaction (OER) and Pt/C for hydrogen evolution reaction (HER), respectively. HER and OER electrocatalysts usually require very different pH values to keep them stable and active. Thus, the development of earth‐abundant nonprecious metal catalysts for both HER and OER is of great importance to practical applications. This work reports the results of integrated water electrolysis using the hybrids of electrospun La_0.5(Ba_0.4Sr_0.4Ca_0.2)_0.5Co_0.8Fe_0.2O_3–δ (L‐0.5) perovskite nanorods attached to reduced graphene oxide (rGO) nanosheets as bifunctional electrodes. Via rationalizing the composition and morphology of L‐0.5/rGO nanohybrids, excellent catalytic performance and stability toward OER and HER are achieved in alkaline media. The operating voltage of integrated L‐0.5/rGO electrolyzer is tested to be 1.76 V at 50 mA cm^–2, which is close to that of the commercially available IrO₂/C‐Pt/C couple (1.76 V @ 50 mA cm^–2). Such a bifunctional electrocatalyst could be extended toward practical electrolysis use with low expanse and high efficiency. More generally, the protocol described here broadens our horizons in terms of the designs and the diverse functionalities of catalysts for use in various applications.     

A Review of Phosphide‐Based Materials for Electrocatalytic Hydrogen Evolution

Hydrogen evolution by means of electrocatalytic water‐splitting is pivotal for efficient and economical production of hydrogen, which relies on the development of inexpensive, highly active catalysts. In addition to sulfides, the search for non‐noble metal catalysts has been mainly directed at phosphides due to the superb activity of phosphides for hydrogen evolution reaction (HER) and their low‐cost considering the abundance of the non‐noble constituents of phosphides. Here, recent research focusing on phosphides is summarized based on their synthetic methodology. A comparative study of the catalytic activity of different phosphides towards HER is then conducted. The catalytic activity is evaluated by overpotentials at fixed current density, Tafel slope, turnover frequency, and the Gibbs free energy of hydrogen adsorption. Based on the methods discussed, perspectives for the various methods of phosphides synthesis are given, and the origins of the high activity and the role of phosphorus on the improved activity towards HER are discussed.     

Electroless Plating of Highly Efficient Bifunctional Boride‐Based Electrodes toward Practical Overall Water Splitting

Exploring highly‐efficient and low‐cost electrodes for both hydrogen and oxygen evolution reaction (HER and OER) is of primary importance to economical water splitting. Herein, a series of novel and robust bifunctional boride‐based electrodes are successfully fabricated using a versatile Et₂NHBH₃‐involved electroless plating (EP) approach via deposition of nonprecious boride‐based catalysts on various substrates. Owing to the unique binder‐free porous nodule structure induced by the hydrogen release EP reaction, most of the nonprecious boride‐based electrodes are highly efficient for overall water splitting. As a distinctive example, the Co‐B/Ni electrode can afford 10 mA cm^?2 at overpotentials of only 70 mV for HER and 140 mV for OER, and can also survive at large current density of 1000 mA cm^?2 for over 20 h without performance degradation in 1.0 m KOH. Several boride‐based two‐electrode electrolyzers can achieve 10 mA cm^?2 at low voltages of around 1.4 V. Moreover, the facile EP approach is economically viable for flexible and large size electrode production.     

Recent Progress in Electrocatalysts for Acidic Water Oxidation

Hydrogen is a clean and renewable energy carrier for powering future transportation and other applications. Water electrolysis is a promising option for hydrogen production from renewable resources such as wind and solar energy. To date, tremendous efforts have been devoted to the development of electrocatalysts and membranes for water electrolysis technology. In principle, water electrolysis in acidic media has several advantages over that in alkaline media, including favorable reaction kinetics, easy product separation, and low operating pressure. However, acidic water electrolysis poses higher requirements for the catalysts, especially the ones for the oxygen evolution reaction. It is a grand challenge to develop highly active, durable, and cost‐effective catalysts to replace precious metal catalysts for acidic water oxidation. In this article, an overview is presented of the latest developments in design and synthesis of electrocatalysts for acidic water oxidation, emphasizing new strategies for achieving high electrocatalytic activity while maintaining excellent durability at low cost. In particular, the reaction pathways and intermediates are discussed in detail to gain deeper insight into the oxygen evolution reaction mechanism, which is vital to rational design of more efficient electrocatalysts. Further, the remaining scientific challenges and possible strategies to overcome them are outlined, together with perspectives for future‐generation electrocatalysts that exploit nanoscale materials for water electrolysis.     

Ultrafine Metal Nanoparticles/N‐Doped Porous Carbon Hybrids Coated on Carbon Fibers as Flexible and Binder‐Free Water Splitting Catalysts

By employing in situ reduction of metal precursor and metal‐assisted carbon etching process, this study achieves a series of ultrafine transition metal‐based nanoparticles (Ni–Fe, Ni–Mo) embedded in N‐doped carbon, which are found efficient catalysts for electrolytic water splitting. The as‐prepared hybrid materials demonstrate outstanding catalytic activities as non‐noble metal electrodes rendered by the synergistic effect of bimetal elements and N‐dopants, the improved electrical conductivity, and hydrophilism. Ni/Mo₂C@N‐doped porous carbon (NiMo‐polyvinylpyrrolidone (PVP)) and NiFe@N‐doped carbon (NiFe‐PVP) produce low overpotentials of 130 and 297 mV at a current density of 10 mA cm^?2 as catalysts for hydrogen evolution reaction and oxygen evolution reaction, respectively. In addition, these binder‐free electrodes show long‐term stability. Overall water splitting is also demonstrated based on the couple of NiMo‐PVP||NiFe‐PVP catalyzer. This represents a simple and effective synthesis method toward a new type of nanometal–carbon hybrid electrodes.     

Recent Advancement of p‐ and d‐Block Elements,Single Atoms,and Graphene‐Based Photoelectrochemical Electrodes for Water Splitting

Solar‐assisted photoelectrochemical (PEC) water splitting to produce hydrogen energy is considered the most promising solution for clean, green, and renewable sources of energy. For scaled production of hydrogen and oxygen, highly active, robust, and cost‐effective PEC electrodes are required. However, most of the available semiconductors as a PEC electrodes have poor light absorption, material degradation, charge separation, and transportability, which result in very low efficiency for photo‐water splitting. Generally, a promising photoelectrode is obtained when the surface of the semiconductor is modified/decorated with a suitable co‐catalyst because it increases the light absorbance spectrum and prevents electron–hole recombination during photoelectrode reactions. In this regard, numerous p‐ and d‐block elements, single atoms, and graphene‐based PEC electrodes have been widely used as semiconductor/co‐catalyst junctions to boost the performances of PEC overall water splitting. This review enumerates the recent progress and applications of p‐ and d‐block elements, single atoms, and graphene‐based PEC electrodes for water splitting. The focus is placed on fundamental mechanism, efficiency, cells design, and various aspects that contribute to the large‐scale prototype device. Finally, future perspectives, summary, challenges, and outlook for improving the activity of PEC photoelectrodes toward whole‐cell water splitting are addressed.