Carbon Dioxide Hydrogenation over a Metal-Free Carbon-Based Catalyst

被引:93
作者
Wu, Jingjie [1 ]
Wen, Cun [2 ]
Zou, Xiaolong [3 ]
Jimenez, Juan [2 ]
Sun, Jing [4 ]
Xia, Yujian [5 ]
Rodrigues, Marco-Tulio Fonseca [1 ]
Vinod, Soumya [1 ]
Zhong, Jun [5 ]
Chopra, Nitin [6 ]
Odeh, Ihab N. [6 ]
Ding, Guqiao [4 ]
Lauterbach, Jochen [2 ]
Ajayan, Pulickel M. [1 ]
机构
[1] Rice Univ, Dept Mat Sci & NanoEngn, Houston, TX 77005 USA
[2] Univ South Carolina, Dept Chem Engn, Columbia, SC 29201 USA
[3] Tsinghua Univ, Tsinghua Berkeley Shenzhen Inst, Shenzhen 518055, Guangdong, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Funct Mat Informat, Shanghai 200050, Peoples R China
[5] Soochow Univ, Inst Funct Nano & Soft Mat Lab FUNSOM, Suzhou 215123, Peoples R China
[6] Saudi Basic Ind Corp SABIC, Sugar Land, TX 77478 USA
关键词
CO2; hydrogenation; graphene quantum dots; N doping; methane; CO2; METHANATION; ADSORPTION; REDUCTION; FORMATE; CHALLENGES; CONVERSION; METHANOL;
D O I
10.1021/acscatal.7b00729
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The hydrogenation of CO2 into useful chemicals provides an industrial-scale pathway for CO2 recycling. The lack of effective thermochemical catalysts currently precludes this process, since it is challenging to identify structures that can simultaneously exhibit high activity and selectivity for this reaction. Here, we report, for the first time, the use of nitrogen doped graphene quantum dots (NGQDs) as metal-free catalysts for CO2 hydrogenation. The nitrogen dopants, located at the edge Sites, play a key role in inducing thermocatalytic activity in carbon nanostructures. Furthermore, the thermocatalytic activity and selectivity of NGQDs are governed by the doped N configurations and their corresponding defect density. The increase of pydinic N concentration at the edge site of NGQDs leads to lower initial reaction temperature for CO2 reduction and also higher CO2 conversion and selectivity toward CH4 over CO.
引用
收藏
页码:4497 / 4503
页数:7
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