| Literature DB >> 34697492 |
Shaoyun Hao1, Hongyuan Sheng2, Min Liu3, Jinzhen Huang2,4, Guokui Zheng1, Fan Zhang1, Xiangnan Liu1, Zhiwei Su1, Jiajun Hu1, Yang Qian1, Lina Zhou1, Yi He1, Bo Song4, Lecheng Lei1,5, Xingwang Zhang6,7, Song Jin8.
Abstract
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.Entities:
Year: 2021 PMID: 34697492 DOI: 10.1038/s41565-021-00986-1
Source DB: PubMed Journal: Nat Nanotechnol ISSN: 1748-3387 Impact factor: 39.213