中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Very highly efficient reduction of CO2 to CH4 using metal-free N-doped carbon electrodes

文献类型:期刊论文

作者Sun, Xiaofu; Kang, Xinchen; Zhu, Qinggong; Ma, Jun; Yang, Guanying; Liu, Zhimin; Han, Buxing
刊名CHEMICAL SCIENCE
出版日期2016
卷号7期号:4页码:2883-2887
英文摘要The electrocatalytic reduction of CO2 to energy-rich chemicals is a promising pathway for energy storage and utilization. Herein we report the first work on the electrocatalytic reduction of CO2 to CH4 using metal-free electrodes. It was found that N-doped carbon (graphene-like) material/carbon paper electrodes were very efficient for the electrochemical reaction when using ionic liquids (ILs) as the electrolytes. The faradaic efficiency of CH4 could be as high as 93.5%, which is the highest to date. The current density was about 6 times higher than that of a Cu electrode under similar conditions, which is the well-known effective electrode for the electrocatalytic reduction of CO2 to CH4. Additionally, a trace amount of water in the IL could improve the current density effectively without reducing CH4 selectivity considerably. Our results highlight a new class of low-cost and designable electrocatalysts for synthetic fuel production from CO2.
收录类别SCI
语种英语
源URL[http://ir.iccas.ac.cn/handle/121111/35923]  
专题化学研究所_胶体、界面与化学热力学实验室
作者单位Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Key Lab Colloid & Interface & Thermodynam, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Sun, Xiaofu,Kang, Xinchen,Zhu, Qinggong,et al. Very highly efficient reduction of CO2 to CH4 using metal-free N-doped carbon electrodes[J]. CHEMICAL SCIENCE,2016,7(4):2883-2887.
APA Sun, Xiaofu.,Kang, Xinchen.,Zhu, Qinggong.,Ma, Jun.,Yang, Guanying.,...&Han, Buxing.(2016).Very highly efficient reduction of CO2 to CH4 using metal-free N-doped carbon electrodes.CHEMICAL SCIENCE,7(4),2883-2887.
MLA Sun, Xiaofu,et al."Very highly efficient reduction of CO2 to CH4 using metal-free N-doped carbon electrodes".CHEMICAL SCIENCE 7.4(2016):2883-2887.

入库方式: OAI收割

来源:化学研究所

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