材料科学
亥姆霍兹自由能
氢
氢键
平面(几何)
化学物理
工程物理
热力学
分子
有机化学
几何学
物理
数学
化学
作者
Xinyu Chen,Bianjing Sun,Qunliang Song,Zengbin Wang,Chenchen Qin,Muhammad Amjad Majeed,Chuntao Chen,Dongping Sun,Kai Zhang,Ming Zhao
标识
DOI:10.1002/adfm.202503701
摘要
Abstract The role of the hydrogen bond network (HBN) within the Helmholtz plane (HP) in regulating the hydrogen evolution kinetics for catalyst development remains ambiguous owing to the lack of fundamental understanding. Herein, leveraging ab initio molecular dynamics simulations, it is discovered that introducing weak metal bonds in Ru/RuO 2 remarkably reshapes the HBN. Subsequently, Ru/RuO 2 nanosheets loaded with single Ga atoms (Ga SA ‐Ru/RuO 2 ) are successfully synthesized using a one‐step annealing strategy. In situ characterizations and theoretical calculations demonstrate that the atomic electric field generated by the weak Ru─Ga bonds can further improve the proportion of 4‐coordinated hydrogen‐bonded water and free water, thus ensuring the sufficient supply of reactants under high current density. Especially, the Ga SA ‐Ru/RuO 2 ‐based anion exchange membrane water electrolyzers (AEMWEs) require only 1.69 and 1.84 V to reach an industrial current density of 1,000 mA cm⁻ 2 in alkaline water and seawater conditions, respectively, and operate stably for 200 h. This study offers an atomic‐level perspective for designing highly efficient catalysts for alkaline hydrogen production.
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