Wang Xiaomei, Long Guifa, Liu Bo, Li Zelong, Gao Wensheng, Zhang Pengfei, Zhang Hong, Zhou Xia, Duan Ruizhi, Hu Wei, Li Can
Key Laboratory of advanced catalysis, Gansu Province, State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, 730000, Lanzhou, China.
Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, School of Chemistry and Chemical Engineering, Guangxi Minzu University, 530008, Nanning, China.
Angew Chem Int Ed Engl. 2023 May 2;62(19):e202301562. doi: 10.1002/anie.202301562. Epub 2023 Mar 30.
Identifying electrocatalysts with functions of easy dissociation of water, rapid transformation of hydroxyl and facile hydrogen-hydrogen bond formation are indispensable while challenge for realizing efficient alkaline hydrogen evolution reaction (HER). Herein, we presented the design of Ni Sn -NiSnO nanocomposites towards addressing this challenge. We showed that Ni Sn possessed ideal hydrogen adsorption and low hydroxyl adsorption abilities and NiSnO facilitated water dissociation and hydroxyl transfer process, respectively. Consequently, the fine-tuned interplay of the two functional parts realized the mutual coordination among the multiple functions and led to significantly boosted HER kinetics. Current densities of 10 and 1000 mA cm were obtained at overpotentials of 14 and 165 mV on the optimized catalyst. This work highlights the significance of considering intrinsic interactions between active sites and all pertinent intermediates on obtaining promising electrocatalysts.
识别具有易于水离解、羟基快速转化和易于形成氢-氢键功能的电催化剂对于实现高效碱性析氢反应(HER)而言不可或缺,但同时也具有挑战性。在此,我们展示了用于应对这一挑战的NiSn-NiSnO纳米复合材料的设计。我们表明,NiSn具有理想的氢吸附能力和低羟基吸附能力,而NiSnO分别促进了水离解和羟基转移过程。因此,两个功能部分之间的微调相互作用实现了多种功能之间的相互协调,并显著提高了析氢反应动力学。在优化后的催化剂上,过电位为14和165 mV时分别获得了10和1000 mA cm的电流密度。这项工作突出了在获得有前景的电催化剂时考虑活性位点与所有相关中间体之间内在相互作用的重要性。