4.8 Article

B-O Bonds in Ultrathin Boron Nitride Nanosheets to Promote Photocatalytic Carbon Dioxide Conversion

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 12, Issue 8, Pages 9935-9943

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.9b21157

Keywords

B-O bond; h-BN; oxygen modification; electron-delivery channel; photocatalytic CO2 conversion

Funding

  1. National Natural Science Foundation of China [U1862111]
  2. Sichuan Provincial International Cooperation Project [2017HH0030, 2019YFH0164]
  3. Innovative Research Team of Sichuan Province [2016TD0011]
  4. Graduate Scientific Research Innovation Foundation of SWPU [2019cxyb013]

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Limited by the chemical inertness of CO2 and the high dissociation energy of the C=O bond, photocatalytic CO2 conversion is highly challenging. Herein, we prepare ultrathin oxygen-modified h-BN (O/BN) nanosheets containing B-O bonds. On the O/BN surface, CO2 can be chemically captured and is bonded with the B-O bond, leading to the formation of an O-B-O bond. This new chemical bond acting as an electron-delivery channel strengthens the interaction between CO2 and the surface. Thus, the reactants can continuously obtain electrons from the surface through this channel. Therefore, the majority of gaseous CO2 directly converts into carbon active species that are detected by in situ DRIFTS over O/BN. Moreover, the activated energies of CO2 conversion are significantly reduced with the introduction of the B-O bond evidenced by DFT calculations. As a result, O/BN nanosheets present an enhanced photocatalytic CO2 conversion performance with the H-2 and CO generation rates of 3.3 and 12.5 mu mol g(-1) h(-1), respectively. This work could help in realizing the effects of nonmetal chemical bonds in the CO2 photoreduction reaction for designing efficient photocatalysts.

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