Noble-Metal-Free CdS Nanoparticle-Coated Graphene Oxide Nanosheets Favoring Electron Transfer for Efficient Photoreduction of CO2

被引:47
作者
Zhu, Lei [1 ]
Liu, Yi [1 ,2 ]
Peng, Xingcui [2 ]
Li, Yibao [1 ]
Men, Yu-Long [2 ]
Liu, Peng [2 ]
Pan, Yun-Xiang [1 ,2 ]
机构
[1] Gannan Normal Univ, Key Lab Organopharmaceut Chem, Ganzhou 341000, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Elect Informat & Elect Engn, Dept Instrument Sci & Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
graphene oxide nanosheets; carbon dioxide; photoreduction; noncovalent functionalization; conductivity; ENERGY-CONVERSION; QUANTUM DOTS; INDIUM-OXIDE; REDUCTION; CARBON; DIANHYDRIDE; FUNCTIONALIZATION; CHALLENGES; CHEMISTRY; CH4;
D O I
10.1021/acsami.0c00163
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Graphene oxide (GO) nanosheets are promising noble-metal-free catalysts. However, the catalytic activity and selectivity of GO are still very low. Herein, GO is first functionalized via noncovalent interactions by an aspartic acid modified anhydride having COOH groups to form A-GO. A-GO is more conductive and hydrophilic than GO and P-GO synthesized via functionalizing GO by a COOH-free anhydride. Then, we load CdS nanoparticles, which are responsible for absorbing light to produce charge carriers, on A-GO to fabricate a CdS/A-GO photocatalyst without noble metals for the photoreduction of CO2 by H2O. CdS/A-GO exhibits a higher photoreduction efficiency than that of CdS/GO and CdS/P-GO. The main carbon-based photoreduction product of CdS/A-GO is CH3OH, whereas that of CdS/GO and CdS/P-GO is CO. The more conductive and hydrophilic A-GO triggers a more efficient electron transfer, CO2 adsorption, and production of hydrogen atoms from H2O dissociation, thus leading to the higher photoreduction efficiency and product change on CdS/A-GO. Besides, the COOH groups of the aspartic acid modified anhydride supply their hydrogen atoms to promote the conversion from CO2 to CH3OH on CdS/A-GO. Therefore, noncovalently functionalizing GO with different active species can efficiently improve the catalytic performance of GO. This opens a new way to design and construct noble-metal-free catalysts with enhanced activity and selectivity.
引用
收藏
页码:12892 / 12900
页数:9
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