共 50 条
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
来源:
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.
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页码:558 / 570
页数:13
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