4.8 Article

Photocatalytic H2Evolution from Ammonia Borane: Improvement of Charge Separation and Directional Charge Transmission

Journal

CHEMSUSCHEM
Volume 13, Issue 19, Pages 5264-5272

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202001536

Keywords

cobalt; hydrogen evolution; hydrogen storage; layered double hydroxides; photocatalysis

Funding

  1. Natural Science Foundation Project of CQ [cstc2018jcyjAX0735, cstc2019jcyj-msxmX0641]
  2. National Natural Science Foundation of China [21201184]
  3. Ministry of Education of Chongqing [KJQN201900811]
  4. Chongqing Technology and Business University [950119090]
  5. Chongqing Key Laboratory of Catalysis, New Environmental Materials [KFJJ2019082]
  6. Key Disciplines of Chemical Engineering and Technology in Chongqing Colleges and Universities during the 13th Five Year Plan and Innovation Group of New Technologies for Industrial Pollution Control of Chongqing Education Commission [CXQT19023]

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Co/(MFe)-Fe-II layered double hydroxide (LDH) LDH photocatalysts have been designed from the aspect of employing stable half-filled Fe(3+)to trap photogenerated electrons, adjusting the M-II-O-Fe oxo-bridged structure to optimize the short-range directional charge transmission and intercalating oxometallate anions into the LDH to further improve light absorption along with electron-hole separation and non-noble metal Co NP loading and reduction to form a heterojunction. These LDH-based photocatalysts are employed for photocatalytic H(2)evolution from ammonia borane in aqueous solution under visible light at 298 K. The photocatalytic H(2)evolution activity is greatly improved through adjustment of the M-II-O-Fe oxo-bridged structure and molybdate intercalation into the LDH. Turnover frequencies of up to 113.2 min(-1)are achieved with Co/CoFe-Mo. Alongside the experimental results and materials characterization, capture experiments and in situ DRIFTS analysis are carried out to study the photocatalytic hydrogen production mechanism.

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