Boosting CO2 Conversion with Terminal Alkynes by Molecular Architecture of Graphene Oxide-Supported Ag Nanoparticles

被引:51
|
作者
Zhang, Xiaofei [1 ]
Liu, Haitao [2 ]
Shi, Yanan [1 ,3 ,4 ]
Han, Jianyu [1 ]
Yang, Zhongjie [1 ,3 ]
Zhang, Yin [1 ]
Long, Chang [1 ]
Guo, Jun [1 ]
Zhu, Yanfei [1 ,3 ]
Qiu, Xueying [1 ]
Xue, Guangxin [1 ]
Zhang, Lingjuan [1 ]
Zhang, Binghao [1 ]
Chang, Lin [1 ]
Tang, Zhiyong [1 ,3 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Nanosyst & Hierarch Fabricat, Beijing 100190, Peoples R China
[2] Inst Appl Phys & Computat Math, Lab Computat Phys, Beijing 100088, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Tsinghua Univ, Dept Chem, Key Lab Organ Optoelect & Mol Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; CARBON-DIOXIDE; CATALYZED CARBOXYLATION; CAPTURE; EFFICIENCY; FIXATION; MILD;
D O I
10.1016/j.matt.2020.07.022
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Carboxylation of terminal alkynes with CO2 via direct C-H bond activation is a highly appealing way to capture and convert CO2 but faces great challenges and difficulty. Here, we report an efficient catalyst that is prepared simply through introduction of p-tert-butylaniline into graphite oxide powders followed by localized growth of Ag nanoparticles (NPs). The bulky nature of p-tert-butylaniline facilitates the powder exfoliation, giving rise to mass production of uniform modified graphene oxide (tert-GO) nanosheets of 4 nm in thickness. Notably, Ag/tert-GO shows excellent catalytic activity for converting alkynes regardless of containing electron-donating or electron-withdrawing groups under mild reaction conditions. The synergy of the amide linkages on tert-GO nanosheets and the supported small-sized Ag NPs is recognized as the vital role in promoting adsorption of CO2 and subsequent conversion.
引用
收藏
页码:558 / 570
页数:13
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