Journal
CHINESE JOURNAL OF CATALYSIS
Volume 42, Issue 10, Pages 1798-1807Publisher
SCIENCE PRESS
DOI: 10.1016/S1872-2067(21)63808-1
Keywords
Tungsten carbide; Doping; Surficial engineering; Hydrogen evolution reaction; Electrocatalyst
Funding
- National Natural Science Foundation of China [51572301]
- National Key R&D Program of China [2017YFB0306000]
- Hunan Provincial Natural Science Foundation [2016JJ3153]
- Innovation-Driven Project of Central South University [502221802]
- Double First-class Funding Project of Central South University
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The study demonstrates the successful synthesis of active and stable P-mounting W2C (WCP) catalyst for hydrogen evolution reactions (HER) under both acidic and alkaline conditions. By controlling the amount of phosphorus sources, the surface mounting level of phosphorus on W2C nanoislands can be regulated to enhance the catalytic activity per active site. This finding highlights the correlation between surface foreign atom-mounting and catalytic activity, providing insights for optimizing the performance of earth-abundant electrocatalysts.
Controllably mounting foreign atoms on the surfaces of earth-abundant electrocatalysts strongly improve their surface electronic properties for optimizing the catalytic performance of surficial sites to an unusual level, and provides a good platform to gain deep insights into catalytic reactions. The present work describes, employing ultrafine W2C nanoislands (average size: 2.3 nm) monodispersed on the N, P dual-doped carbon frameworks as a model system, how to regulate the atomic phosphorous-mounting effect on the surfaces of W2C to derive an active and stable P-mounting W2C (WCP) catalyst for both acidic and alkaline hydrogen evolution reaction (HER). Since in situ phosphorus substitution into carbon sites of preformed W2C nanoislands gradually proceeds from surfaces to solids, so that using a proper amount of phosphorus sources can readily control the surface mounting level to avoid the mass P-doping into the bulk. By this way, the activity per active site of WCP catalyst with robust stability can be optimized to 0.07 and 0.56 H-2 s(-1) at -200 mV overpotential in acid and base, respectively, which reach up to the several-fold of pure-phase W2C (0.01 and 0.05 H-2 s(-1)). Theoretical investigations suggest that compared with solid P doping, the P mounting on W2C surface can more remarkably enhance its metallicity and decrease the hydrogen release barrier. This finding disclosed a key correlation between surface foreign atom-mounting and catalytic activity, and suggested a logical extension to other earth-abundant catalysts for various catalytic reactions. (C) 2021, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
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