过电位
催化作用
贵金属
析氧
分解水
晶界
材料科学
吸附
铱
膜
质子交换膜燃料电池
氧气
化学
无机化学
氧化物
电化学
化学工程
物理化学
光催化
冶金
电极
有机化学
工程类
微观结构
生物化学
作者
Shaoyun Hao,Hongyuan Sheng,Min Liu,Jinzhen Huang,Guokui Zheng,Fan Zhang,Xiangnan Liu,Zhiwei Su,Jiajun Hu,Yang Qian,Lina Zhou,Yi He,Bo Song,Lecheng Lei,Xingwang Zhang,Song Jin
标识
DOI:10.1038/s41565-021-00986-1
摘要
Acidic oxygen evolution reaction is crucial for practical proton exchange membrane water splitting electrolysers, which have been hindered by the high catalytic overpotential and high loading of noble metal catalysts. Here we present a torsion-strained Ta0.1Tm0.1Ir0.8O2-δ nanocatalyst with numerous grain boundaries that exhibit a low overpotential of 198 mV at 10 mA cm-2 towards oxygen evolution reaction in 0.5 M H2SO4. Microstructural analyses, X-ray absorption spectroscopy and theoretical calculations reveal that the synergistic effects between grain boundaries that result in torsion-strained Ir-O bonds and the doping induced ligand effect collectively tune the adsorption energy of oxygen intermediates, thus enhancing the catalytic activity. A proton exchange membrane electrolyser using a Ta0.1Tm0.1Ir0.8O2-δ nanocatalyst with a low mass loading of 0.2 mg cm-2 can operate stably at 1.5 A cm-2 for 500 hours with an estimated cost of US$1 per kilogram of H2, which is much lower than the target (US$2 per kg of H2) set by the US Department of Energy.
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