Three-Phase Photocatalysis for the Enhanced Selectivity and Activity of CO2 Reduction on a Hydrophobic Surface

被引:334
作者
Li, Ang [1 ,2 ]
Cao, Qian [2 ]
Zhou, Guangye [3 ]
Schmidt, Bernhard V. K. J. [2 ]
Zhu, Wenjin [3 ]
Yuan, Xintong [3 ]
Huo, Hailing [4 ]
Gong, Jinlong [3 ]
Antonietti, Markus [2 ]
机构
[1] Nanjing Univ Sci & Technol, Dept Appl Phys, Xiaolingwei St 200, Nanjing 210094, Jiangsu, Peoples R China
[2] Max Planck Inst Colloids & Interfaces, D-14476 Potsdam, Germany
[3] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Sch Chem Engn & Technol, Key Lab Green Chem Technol,Minist Educ, Weijin Rd 92, Tianjin 300072, Peoples R China
[4] Shanxi Datong Univ, Sch Chem & Environm Engn, Xingyun St 405, Datong 037009, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon nitride; CO2; reduction; hydrophobic material; photocatalysis; three-phase catalysis; YOLK-SHELL NANOSTRUCTURES; VISIBLE-LIGHT; CARBON NITRIDE; HYDROGEN EVOLUTION; EFFICIENT; NANOPARTICLES; POLYMERS; DRIVEN; G-C3N4; DEHYDROGENATION;
D O I
10.1002/anie.201908058
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The photocatalytic CO2 reduction reaction (CRR) represents a promising route for the clean utilization of stranded renewable resources, but poor selectivity resulting from the competing hydrogen evolution reaction (HER) in aqueous solution limits its practical applicability. In the present contribution a photocatalyst with hydrophobic surfaces was fabricated. It facilitates an efficient three-phase contact of CO2 (gas), H2O (liquid), and catalyst (solid). Thus, concentrated CO2 molecules in the gas phase contact the catalyst surface directly, and can overcome the mass-transfer limitations of CO2, inhibit the HER because of lowering proton contacts, and overall enhance the CRR. Even when loaded with platinum nanoparticles, one of the most efficient HER promotion cocatalysts, the three-phase photocatalyst maintains a selectivity of 87.9 %. Overall, three-phase photocatalysis provides a general and reliable method to enhance the competitiveness of the CRR.
引用
收藏
页码:14549 / 14555
页数:7
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