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Hydrogenation reactions are industrially important reactions that typically require unfavorably high H2 pressure and temperature for many functional groups. Herein we reveal surprisingly strong size-dependent activity of Pt nanoparticles (PtNPs) in catalyzing this reaction. Based on unambiguous spectral analyses, the size effect has been rationalized by the size-dependent d-band electron structure of the PtNPs. This understanding enables production of a catalyst with size of 1.2 nm, which shows a sixfold increase in turnover frequency and 28-fold increase in mass activity in the regioselective hydrogenation of quinoline, compared with PtNPs of 5.3 nm, allowing the reaction to proceed under ambient conditions with unprecedentedly high reaction rates. The size effect and the synthesis strategy developed herein may provide a general methodology in the design of metal-nanoparticle-based catalysts for a broad range of organic syntheses.

作者:Licheng, Bai;Xin, Wang;Qiang, Chen;Yifan, Ye;Haoquan, Zheng;Jinghua, Guo;Yadong, Yin;Chuanbo, Gao

来源:Angewandte Chemie (International ed. in English) 2016 年 55卷 50期

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作者:
Licheng, Bai;Xin, Wang;Qiang, Chen;Yifan, Ye;Haoquan, Zheng;Jinghua, Guo;Yadong, Yin;Chuanbo, Gao
来源:
Angewandte Chemie (International ed. in English) 2016 年 55卷 50期
标签:
d-band electron structure heterogeneous catalysis hydrogenation reactions platinum nanoparticles size effects
Hydrogenation reactions are industrially important reactions that typically require unfavorably high H2 pressure and temperature for many functional groups. Herein we reveal surprisingly strong size-dependent activity of Pt nanoparticles (PtNPs) in catalyzing this reaction. Based on unambiguous spectral analyses, the size effect has been rationalized by the size-dependent d-band electron structure of the PtNPs. This understanding enables production of a catalyst with size of 1.2 nm, which shows a sixfold increase in turnover frequency and 28-fold increase in mass activity in the regioselective hydrogenation of quinoline, compared with PtNPs of 5.3 nm, allowing the reaction to proceed under ambient conditions with unprecedentedly high reaction rates. The size effect and the synthesis strategy developed herein may provide a general methodology in the design of metal-nanoparticle-based catalysts for a broad range of organic syntheses.