A Derivative of ZnIn2S4 Nanosheet Supported Pd Boosts Selective CO2 Hydrogenation

被引:6
|
作者
Wang, Kuncan [1 ,2 ]
Zhu, Yuanmin [3 ,4 ,5 ]
Gu, Meng [5 ]
Hu, Zhiwei [6 ]
Chang, Yu-Chung [7 ]
Pao, Chih-Wen [7 ]
Xu, Yong [1 ]
Huang, Xiaoqing [2 ]
机构
[1] Guangdong Univ Technol, Sch Mat & Energy, Collaborat Innovat Ctr Adv Energy Mat, Guangzhou Key Lab Low Dimens Mat & Energy Storage, Guangzhou 510006, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[3] Dongguan Univ Technol, Res Inst Interdisciplinary Sci, Dongguan 523808, Peoples R China
[4] Dongguan Univ Technol, Sch Mat Sci & Engn, Dongguan 523808, Peoples R China
[5] Southern Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen 518055, Peoples R China
[6] Max Planck Inst Chem Phys Solids, Nothnitzer Str 40, D-01187 Dresden, Germany
[7] Natl Synchrotron Radiat Res Ctr, 101 Hsin Ann Rd, Hsinchu 30076, Taiwan
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
anti-sintering; CO2; hydrogenation; In2O3; S doped support; ZnIn2S4; nanosheets; METHANOL SYNTHESIS; CATALYSTS; CARBON; SITE;
D O I
10.1002/adfm.202215148
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO2 hydrogenation to value-added chemicals has been considered as a promising way to reduce CO2 emission and alleviate energy crisis. However, the high-efficiency CO2 hydrogenation process is driven by the current drawbacks of low activity and/or selectivity. Herein, it is demonstrated that 2D S-doped ZnInOx, which evolves from the calcination of ZnIn2S4 nanosheets (ZIS NSs), can serve as a functional support for Pd nanoparticles (NPs) to promote the selective CO2 hydrogenation to CH3OH. Detailed investigations show that ZnIn2S4 will evolve into In2O3 and amorphous S-doped ZnO, on which Pd NPs are preferentially located due to the strong electrophilicity of S. Consequently, the strong interaction between Pd NPs and amorphous S-doped ZnO prevents Pd NPs from sintering and facilitates the selective CO2 hydrogenation to produce CH3OH. The optimal catalyst shows a CO2 conversion of 12.7% with a CH3OH selectivity of 87.4% at 280 degrees C. This study provides a facile route to regulate catalytic supports and controllably load active species, which may attract great research interests in the fields of heterogeneous catalysis.
引用
收藏
页数:8
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