海水
过电位
氢
催化作用
摄动(天文学)
电流密度
材料科学
耐久性
制氢
化学物理
化学
化学工程
无机化学
电化学
物理化学
物理
电极
有机化学
地质学
复合材料
工程类
量子力学
海洋学
作者
Nanzhu Nie,Dan Zhang,Zuochao Wang,Shijie Ge,Yanli Gu,Bo Yang,Jianping Lai,Lei Wang
标识
DOI:10.1016/j.apcatb.2022.122100
摘要
Achieving acidic seawater hydrogen production under commercial current densities remains a challenge. We present here a novel strategy through strong metal-support interaction (SMSI) and Pt-p-block alloys ([email protected], M = Ga, In, Pb, and Bi) to construct a stable electronic perturbation and achieve acidic seawater hydrogen evolution performance at commercial current densities for the first time. SMSI stabilizes electronic perturbation and promotes durability up to 360 h. The optimized Pt61Ga39 @CNT exhibits an overpotential of 18 mV at 10 mA cm−2 in 0.5 M H2SO4 and maintains 360 h stability at 500 mA cm−2 in acidic seawater. Density functional theory (DFT) calculation reveals that the optimized d-band center of Pt and ΔGH* increase the catalytic activity, and the higher vacancy formation energy enhances the durability. Overall, this discovery not only first achieves stable acidic seawater hydrogen production under commercial current densities, but also opens a new opportunity to explore catalytic applications of p-block alloys and SMSI stabilized electronic perturbation.
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