| Literature DB >> 29888491 |
Wenxing Chen1,2, Jiajing Pei3, Chun-Ting He4, Jiawei Wan1, Hanlin Ren1, Yu Wang5, Juncai Dong6, Konglin Wu1, Weng-Chon Cheong1, Junjie Mao1, Xusheng Zheng7, Wensheng Yan7, Zhongbin Zhuang3, Chen Chen1, Qing Peng1, Dingsheng Wang1, Yadong Li1.
Abstract
Tungsten-based catalysts are promising candidates to generate hydrogen effectively. In this work, a single-W-atom catalyst supported on metal-organic framework (MOF)-derived N-doped carbon (W-SAC) for efficient electrochemical hydrogen evolution reaction (HER), with high activity and excellent stability is reported. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and X-ray absorption fine structure (XAFS) spectroscopy analysis indicate the atomic dispersion of the W species, and reveal that the W1 N1 C3 moiety may be the favored local structure for the W species. The W-SAC exhibits a low overpotential of 85 mV at a current density of 10 mA cm-2 and a small Tafel slope of 53 mV dec-1 , in 0.1 m KOH solution. The HER activity of the W-SAC is almost equal to that of commercial Pt/C. Density functional theory (DFT) calculation suggests that the unique structure of the W1 N1 C3 moiety plays an important role in enhancing the HER performance. This work gives new insights into the investigation of efficient and practical W-based HER catalysts.Entities:
Keywords: N-doped carbon; electrocatalysts; hydrogen evolution reaction; metal-organic frameworks; single W atoms
Year: 2018 PMID: 29888491 DOI: 10.1002/adma.201800396
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849