4.7 Article

Insights into the unique role of cobalt phosphide for boosting hydrogen evolution activity based on MIL-125-NH2

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 44, Issue 33, Pages 17909-17921

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2019.05.138

Keywords

MIL-125-NH2; Cobalt phosphide; CoP/MIL-125-NH2; Hydrogen evolution; Photocatalysis

Funding

  1. Chinese National Natural Science Foundation [21862002, 41663012]
  2. North Minzu University [ZDZX201803]
  3. Ningxia low-grade resource high value utilization and environmental chemical integration technology innovation team project of North Minzu University
  4. key scientific research projects of North Minzu University [2017KJ16]

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Controllable and efficient photo-catalyst is of particular importance not only for improving photo-catalytic activity of hydrogen evolution, but also for achieving more excellent performance of semiconductors in practical applications. Here two n-type semiconductors (cobalt phosphide (CoP) and MIL-125-NH2) as well as their complex catalysts (CoP/MIL-125NH(2)) are reported and the unique role of cobalt phosphide in CoP/MIL-125-NH2 is systematically investigated for boosting hydrogen evolution activity based on MIL-125-NH2 under visible light-driven. CoP/MIL-125-NH2 can exhibit a 267-fold enhanced catalytic activity compared to the pristine MIL-125-NH2. Moreover, the excellent catalytic property of the as -prepared catalysts has been investigated in detail by several means of characterization. The findings are that the distinctive morphology and relatively ideal S-BET of MIL125-NH2 play particular role in the highly efficient photo-catalytic reaction system, and the highly efficient catalytic property of CoP/MIL-125-NH2 mainly depends on unique role of cobalt phosphide having excellent photo-catalytic performance for hydrogen evolution. Based on the above results, the possible mechanism of photo-catalytic hydrogen evolution is speculated. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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