4.8 Article

Transition metal doping BiOBr nanosheets with oxygen vacancy and exposed {102} facets for visible light nitrogen fixation

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 281, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2020.119516

Keywords

BiOBr nanosheets; Transitional metal-doped; Oxygen vacancies; N-2 photofixation

Funding

  1. NSFC [U1463204, 21872029, 21173045]
  2. 1st Program of Fujian Province for Top Creative Young Talents
  3. Program for Leading Talents of Fujian Universities
  4. Award Program for Minjiang Scholar Professorship
  5. NSF of Fujian Province [2017J07002, 2019J0106]

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Artificial photocatalytic N-2 reduction to NH3 under ambient conditions is a promising alternative to industrial N-2 fixation. This study demonstrated the engineering of BiOBr nanosheets with transition metal doping and oxygen vacancies to enhance visible light N-2 fixation efficiency. The synergy of transition metal doping and oxygen vacancies improved charge carrier separation and electron transfer, leading to enhanced N-2 adsorption and activation ability over modified BiOBr nanosheets.
Artificial photocatalytic N-2 reduction to NH3 under ambient conditions represents a promising alternative way for the industrial N-2 fixation by Haber - Bosch process. This work reports the simultaneous engineering of BiOBr nanosheets with exposed {102} facets by means of transition metal (Fe, Mo, Ni) doping and oxygen vacancies (OVs) that aid to expose internal metal dopants toward efficient visible light N-2 fixation. The synergy of transition metal doping and OVs results in the modulated band structures, improved charge carrier separation as well as electron transfer to N-2, thereby leading to enhanced N-2 adsorption and activation ability over modified BiOBr nanosheets. In particular, the Fe-doped BiOBr with OVs possesses the optimal photocatalytic activity of NH3 yield of 46.1 mu mol g(-1) h(-1) without any sacrificial agent, which is 6-fold that of pristine BiOBr. The findings will shed new light on rational engineering of adsorption, activation sites and charge carrier separation for designing efficient N-2 fixation photocatalysts.

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