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The sustainable and scalable production of hydrogen through hydrogen evolution reaction (HER) and oxygen through oxygen evolution reaction (OER) in water splitting demands efficient and robust electrocatalysts. Currently, state‐of‐the‐art electrocatalysts of Pt and IrO2/RuO2 exhibit the benchmark catalytic activity toward HER and OER, respectively. However, expanding their practical application is hindered by their exorbitant price and scarcity. Therefore, the development of alternative effective electrocatalysts for water splitting is crucial. In the last few decades, substantial effort has been devoted to the development of alternative HER/OER and water splitting catalysts based on various transition metals (including Fe, Co, Ni, Mo, and atomic Pt) which show promising catalytic activities and durability. In this review, after a brief introduction and basic mechanism of HER/OER, the authors systematically discuss the recent progress in design, synthesis, and application of single atom and cluster‐based HER/OER and water splitting catalysts. Moreover, the crucial factors that can tune the activity of catalysts toward HER/OER and water splitting such as morphology, crystal defects, hybridization of metals with nonmetals, heteroatom doping, alloying, and formation of metals inside graphitic layered materials are discussed. Finally, the existing challenges and future perspectives for improving the performance of electrocatalysts for water splitting are addressed.

Noble nanoparticle(NP)-sized electrocatalysts have been exploited for diverse electrochemical reactions, in particular, for eco-friendly hydrogen economy such as water splitting. Recently, minimal amounts of single atoms (SAs) are exploited to...

The most efficient electrocatalyst for the hydrogen evolution reaction (HER) is a Pt‐based catalyst, but its high cost and nonperfect efficiency hinder wide‐ranging industrial/technological applications. Here, an electrocatalyst of both ruthenium (Ru) single atoms (SAs) and N‐doped‐graphitic(GN)‐shell‐covered nitrided‐Ru nanoparticles (NPs) (having a Ru‐Nx shell) embedded on melamine‐derived GN matrix {1: [Ru(SA)+Ru(NP)@RuNx@GN]/GN}, which exhibits superior HER activity in both acidic and basic media, is presented. In 0.5 m H2SO4/1 m KOH solutions, 1 shows diminutive “negative overpotentials” (−η = |η| = 10/7 mV at 10 mA cm−2, lowest ever) and high exchange current densities (4.70/1.96 mA cm−2). The remarkable HER performance is attributed to the near‐zero free energies for hydrogen adsorption/desorption on Ru(SAs) and the increased conductivity of melamine‐derived GN sheets by the presence of nitrided‐Ru(NPs). The nitridation process forming nitrided‐Ru(NPs), which are imperfectly covered by a GN shell, allows superb long‐term operation durability. The catalyst splits water into molecular oxygen and hydrogen at 1.50/1.40 V (in 0.1 m HClO4/1 m KOH), demonstrating its potential as a ready‐to‐use, highly effective energy device for industrial applications.

A simple and effective strategy for fabricating high-stability alkaline anion exchange membrane water electrolyzers for large-scale hydrogen production.

Designing a facile strategy to access active and atomically dispersed metallic catalysts are highly challenging for single atom catalysts (SACs). Herein, a simple and fast approach is demonstrated to construct Pt catalysts with single atoms in large quantity via ball milling Pt precursor and N‐doped carbon support (K2PtCl4@NC‐M; M denotes ball‐milling). The as‐prepared K2PtCl4@NC‐M only requires a low overpotential of 11 mV and exhibits 17‐fold enhanced mass activity for the electrochemical hydrogen evolution compared to commercial 20 wt% Pt/C. The superior hydrogen evolution reaction (HER) catalytic activity of K2PtCl4@NC‐M can be attributed to the generation of Pt single atoms, which improves the utilization efficiency of Pt atoms and the introduction of Pt‐N2C2 active sites with near‐zero hydrogen adsorption energy. This viable ball milling method is found to be universally applicable to the fabrication of other single metal atoms, for example, rhodium and ruthenium (such as Mt‐N2C2, where Mt denotes single metal atom). This strategy also provides a promising and practical avenue toward large‐scale energy storage and conversion application.

For efficient water splitting, it is essential to develop inexpensive and super-efficient electrocatalysts for the oxygen evolution reaction (OER). Herein, we report a phosphate-based electrocatalyst [Fe3Co(PO4)4@reduced-graphene-oxide(rGO)] showing outstanding OER performance (much higher than state-of-the-art Ir/C catalysts), the design of which was aided by first-principles calculations. This electrocatalyst displays low overpotential (237 mV at high current density 100 mA cm−2 in 1 M KOH), high turnover frequency (TOF: 0.54 s−1), high Faradaic efficiency (98%), and long-term durability. Its remarkable performance is ascribed to the optimal free energy for OER at Fe sites and efficient mass/charge transfer. When a Fe3Co(PO4)4@rGO anodic electrode is integrated with a Pt/C cathodic electrode, the electrolyzer requires only 1.45 V to achieve 10 mA cm−2 for whole water splitting in 1 M KOH (1.39 V in 6 M KOH), which is much smaller than commercial Ir-C//Pt-C electrocatalysts. This cost-effective powerful oxygen production material with carbon-supporting substrates offers great promise for water splitting.

Carbon-based transition metal (TM) single-atom catalysts (SACs) have shown a great potential toward electrochemical water splitting and H2 production. Given that two-dimensional (2D) materials are widely exploited for sustainable energy...