Kou Zongkui, Wang Tingting, Wu Haijun, Zheng Lirong, Mu Shichun, Pan Zhenghui, Lyu Zhiyang, Zang Wenjie, Pennycook Stephen J, Wang John
Department of Materials Science and Engineering, National University of Singapore, Singapore, 117574, Singapore.
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, China.
Small. 2019 May;15(19):e1900248. doi: 10.1002/smll.201900248. Epub 2019 Apr 4.
Synergistic integration of two active metal-based compounds can lead to much higher electrocatalytic activity than either of the two individually, due to the interfacial effects. Herein, a proof-of-concept strategy is creatively developed for the successful fabrication of twinned tungsten carbonitride (WCN) nanocrystals, where W C and WN are chemically bonded at the molecule level. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and X-ray absorption fine structure (XAFS) spectroscopy analyses demonstrate that the intergrowth of W C and WN in the WCN nanocrystals produces abundant N-W-C interfaces, leading to a significant enhancement in catalytic activity and stability for hydrogen evolution reaction (HER). Indeed, it shows 14.2 times higher and 140 mV lower in the respective turn-over frequency (TOF) and overpotential at 10 mA cm compared to W C alone. To complement the experimental observation, the theoretical calculations demonstrate that the WCN endows more favorable hydrogen evolution reaction than the single W C or WN crystals due to abundant interfaces, beneficial electronic states, lower work function, and more active W sites at the N-W-C interfaces.
由于界面效应,两种活性金属基化合物的协同整合可导致比单独的两种化合物更高的电催化活性。在此,创造性地开发了一种概念验证策略,用于成功制备孪晶碳氮化钨(WCN)纳米晶体,其中WC和WN在分子水平上化学键合。高角度环形暗场扫描透射电子显微镜(HAADF-STEM)和X射线吸收精细结构(XAFS)光谱分析表明,WCN纳米晶体中WC和WN的共生产生了丰富的N-W-C界面,从而显著提高了析氢反应(HER)的催化活性和稳定性。实际上,与单独的WC相比,它在10 mA cm下的周转频率(TOF)高14.2倍,过电位低140 mV。为补充实验观察结果,理论计算表明,由于丰富的界面、有利的电子态、较低的功函数以及N-W-C界面处更活跃的W位点,WCN赋予了比单一WC或WN晶体更有利的析氢反应。