Green hydrogen is being considered as a next-generation sustainable energy source. It is created electrochemically by water splitting with renewable electricity such as wind, geothermal, solar, and hydropower. The development of electrocatalysts is crucial for the practical production of green hydrogen in order to achieve highly efficient water-splitting systems. Due to its advantages of being environmentally friendly, economically advantageous, and scalable for practical application, electrodeposition is widely used to prepare electrocatalysts. There are still some restrictions on the ability to create highly effective electrocatalysts using electrodeposition owing to the extremely complicated variables required to deposit uniform and large numbers of catalytic active sites. In this review article, we focus on recent advancements in the field of electrodeposition for water splitting, as well as a number of strategies to address current issues. The highly catalytic electrodeposited catalyst systems, including nanostructured layered double hydroxides (LDHs), single-atom catalysts (SACs), high-entropy alloys (HEAs), and core-shell structures, are intensively discussed. Lastly, we offer solutions to current problems and the potential of electrodeposition in upcoming water-splitting electrocatalysts.

Silicon has been considered as a promising anode material due to its high theoretical capacity (3579 mAh g⁻¹), however, it suffers from capacity degradation owing to the series of multiscale fractures in the electrode caused by the volume variation (≈300%) during phase transitions. The molecular/structural design of polymeric binders has been pivotal in overcoming the challenges to improve the integrity of Si anode via strong interactions between active materials and binders. In this respect, the covalently crosslinked polyacrylamide (PAM) network, which effectively maintains its mechanical strength and shape, is introduced as a novel binder system for Si active materials. Unlike the thermal crosslinking, the abundant polar‐functional groups, related to the strong interactions between Si and polymer, are not sacrificed in their network by virtue of the in situ polymerization. Through the PAM gel, the Si‐based electrode exhibits a superior capacity of ≈1526 mAh g⁻¹ at an optimized crosslinker concentration after 500 cycles. In addition, the effect of the chemical/mechanical properties of PAM gel on the electrochemical properties of Si is adequately elucidated. The results will provide meaningful insight regarding the design of novel binders, especially in the application of the covalently crosslinked structure to Si‐based electrodes.