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

被引:97
作者
Cao, Yuehan [1 ,2 ]
Zhang, Ruiyang [2 ]
Zhou, Tianli [2 ]
Jin, Shengming [3 ]
Huang, Jindi [4 ]
Ye, Liqun [5 ]
Huang, Zeai [2 ]
Wang, Fang [2 ]
Zhou, Ying [1 ,2 ]
机构
[1] Southwest Petr Univ, Sch Mat Sci & Engn, State Key Lab Oil & Gas Reservoir Geol & Exploita, Chengdu 610500, Peoples R China
[2] Southwest Petr Univ, Ctr New Energy Mat & Technol, Sch Mat Sci & Engn, Chengdu 610500, Peoples R China
[3] Cent South Univ, Key Lab Mineral Mat & Applicat Hunan Prov, Changsha 410083, Peoples R China
[4] Nanyang Normal Univ, Coll Chem & Pharmaceut Engn, Engn Technol Res Ctr Henan Prov Solar Catalysis, Nanyang 473061, Peoples R China
[5] China Three Gorges Univ, Coll Mat & Chem Engn, Key Lab Inorgan Nonmetall Crystalline & Energy Co, Yichang 443002, Peoples R China
基金
中国国家自然科学基金;
关键词
B-O bond; h-BN; oxygen modification; electron-delivery channel; photocatalytic CO2 conversion; CO2; REDUCTION; SURFACE; FUNCTIONALIZATION; SPECTROSCOPY; MONOLAYER; CHEMICALS; CATALYST; CAPTURE; TIO2;
D O I
10.1021/acsami.9b21157
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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.
引用
收藏
页码:9935 / 9943
页数:9
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