水素発生反応における金属および非金属元素ドープ型電極触媒の相乗効果：レビュー

The hydrogen evolution reaction (HER) is a key electrochemical process for sustainable hydrogen production via water splitting. However, its practical implementation is hindered by sluggish reaction kinetics and reliance on noble metal catalysts like platinum, which are costly and scarce. To overcome these limitations, synergistic doping of metallic (e.g., Fe, Co, Ni, Mo, Mn, Cu, Pt) and non-metallic (e.g., P, N, B, O, S) elements has emerged as an effective strategy to enhance catalytic activity. This dual-doping approach enables fine-tuning of the catalyst's electronic environment, increases active site density, and improves hydrogen adsorption/desorption behaviour. Metallic dopants modulate conductivity and the electronic structure of active sites, while non-metallic heteroatoms introduce charge redistribution, surface defects, and chemical polarity - collectively accelerating HER kinetics. This review critically examines recent advances in the synthesis and performance of heteroatom-doped HER electrocatalysts under acidic and alkaline conditions. Emphasis is placed on how compositional tuning, structural design, and interface engineering contribute to improved catalytic performance, including low overpotentials, favourable Tafel slopes, and long-term stability. These developments underscore the potential of heteroatom doping as a versatile platform for designing next-generation HER catalysts for scalable and economically viable hydrogen energy systems.