Liu Di, Lv Qingqing, Lu Siqi, Fang Jinjie, Zhang Yufeng, Wang Xingdong, Xue Yanrong, Zhu Wei, Zhuang Zhongbin
State Key Lab of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, China.
Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
Nano Lett. 2021 Apr 14;21(7):2809-2816. doi: 10.1021/acs.nanolett.0c04878. Epub 2021 Mar 18.
Proton exchange membrane water electrolyzer can sustainably and environmentally friendly produce hydrogen. However, it is hindered by the lack of high-performance anode catalysts for oxygen evolution reaction (OER) in acid electrolyte. Herein, IrCuNi deeply concave nanocubes (IrCuNi DCNCs) are successfully synthesized from the selective etching of the facet of cubic nanoparticles, and they significantly boost the OER. The obtained IrCuNi DCNCs show high activity toward OER in the acidic electrolyte, which only requires an overpotential of 273 mV to achieve the OER current density of 10 mA cm at a low Ir loading of 6.0 μg cm. The precious metal based mass activity is 6.6 A mg at 1.53 V, which is 19 times as high as that of pristine Ir. It demonstrates that the outstanding catalytic performance is beneficial from the well-defined multimetal concave nanostructures, which may shed light on the fabrication of efficient water electrolyzers.
质子交换膜水电解槽能够可持续且环保地生产氢气。然而,酸性电解质中用于析氧反应(OER)的高性能阳极催化剂的缺乏阻碍了其发展。在此,通过对立方纳米颗粒晶面的选择性蚀刻成功合成了IrCuNi深凹纳米立方体(IrCuNi DCNCs),它们显著提高了析氧反应性能。所制备的IrCuNi DCNCs在酸性电解质中对析氧反应表现出高活性,在低Ir负载量为6.0 μg cm²时,仅需273 mV的过电位就能实现10 mA cm²的析氧反应电流密度。在1.53 V时,基于贵金属的质量活性为6.6 A mg⁻¹,是原始Ir的19倍。这表明优异的催化性能得益于明确的多金属凹面纳米结构,这可能为高效水电解槽的制造提供启示。