One-pot synthesis of nanostructured carbon materials from carbon dioxide via electrolysis in molten carbonate salts

被引:98
|
作者
Wu, Hongjun [1 ]
Li, Zhida [1 ]
Ji, Deqiang [1 ]
Liu, Yue [1 ]
Li, Lili [1 ]
Yuan, Dandan [1 ]
Zhang, Zhonghai [2 ]
Ren, Jiawen [3 ]
Lefler, Matthew [3 ]
Wang, Baohui [1 ]
Licht, Stuart [3 ]
机构
[1] Northeast Petr Univ, Coll Chem & Chem Engn, Prov Key Lab Oil & Gas Chem Technol, Daqing 163318, Peoples R China
[2] E China Normal Univ, Dept Chem, 500 Dongchuan Rd, Shanghai 200241, Peoples R China
[3] George Washington Univ, Dept Chem, Washington, DC 20052 USA
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金; 中国博士后科学基金; 美国国家科学基金会;
关键词
PHOTOCATALYTIC CO2 REDUCTION; THERMAL ELECTROCHEMICAL PRODUCTION; COMPLEXES; CAPTURE; ELECTRODEPOSITION; TEMPERATURE; SOLUBILITY; CONVERSION; BINUCLEAR; FORMATE;
D O I
10.1016/j.carbon.2016.05.031
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
As the primary culprit of greenhouse effect, carbon dioxide has garnered global attention, and the technologies currently being developed to reduce the emission of CO2 vary widely. In this study, CO2 was electrochemically reduced in various molten mixtures of Li-Na-K carbonates to carbon nanomaterials. By regulating the electrolysis current density, electrolyte, and electrolytic temperature, the carbon products had different morphologies of honeycomb-like and nanotubular structures. A transition from a honeycomb/platelet to nanomaterial carbon morphology was observed to occur at similar to 600 degrees C with increase in temperature. The observation of nanostructures is consistent with a higher diversity of structures possible with enhanced rearrangement kinetics that can occur at higher temperature. A high yield of a carbon nanotube (CNT) was not observed from a Li-Na-K electrolyte, no CNTs are formed from a Na-K carbonate electrolyte, but a high yield is observed from pure Li, or mixed Li-Na or mixed Li-Ba carbonate electrolytes, and the carbon nanotube product diameter is observed to increase with increasing electrolysis time. (C) 2016 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:208 / 217
页数:10
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