4.8 Article

Pyrolytic carbon supported alloying metal dichalcogenides as freestanding electrodes for efficient hydrogen evolution

期刊

CARBON
卷 132, 期 -, 页码 512-519

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2018.02.025

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资金

  1. 973 program of China [2015CB932500, 2014CB932401]
  2. National Natural Science Foundation of China [51722207, 51372131]
  3. Beijing Nova Program [Z161100004916099]
  4. Tsinghua University Initiative Scientific Research Program [20151080367]
  5. National Science Foundation under EFRI 2-DARE [1542707]
  6. DOE [DE-SC0018025]

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Electrochemical reduction of water is a renewable way to produce clean hydrogen energy. In order to overcome the high-cost and shortage of noble metals, transition metal compounds involving earth-abundant elements, such as MoS2 and WS2, have been proposed as novel catalysts for hydrogen evolution reaction (HER). Efforts have been made to increase the intrinsic catalytic activity of transition metal dichalcogenides (TMDCs), while alloying same-group elements has not been vastly investigated. Moreover, besides the catalytic activity, the design of free-standing catalytic electrodes is also critical for HER. In this work, we synthesize pyrolytic carbon film with MoxW1-xS2 nanoflakes embedded as a freestanding flexible electrodes for HER catalysis. The pyrolytic carbon acts as conductive and flexible matrix for TMDC alloys with controlled composition, resulting in remarkably enhanced HER activity. The highest HER activity was observed for Mo0.37W0.63S2/C samples with an overpotential of 0.137 V at geometric current densities of j(geo) = 10 mA cm(-2) and a Tafel slope of 53 mV dec(-1). These results now provide low-cost viable alternatives for the design and construction of catalysts based on alloyed TMDCs. (c) 2018 Elsevier Ltd. All rights reserved.

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