Affiliation:
1. College of Chemistry and Molecular Sciences Hubei Key Laboratory of Electrochemical Power Sources Wuhan University Wuhan 430072 P. R. China
2. Center for Alloy Innovation and Design (CAID) State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi An Shi, Xi'an 710049 P. R. China
3. State Key Laboratory of Marine Resource Utilization in South China Sea Hainan University Haikou 570228 P. R. China
Abstract
AbstractTo be successfully implemented, an efficient conversion, affordable operation and high values of CO2‐derived products by electrochemical conversion of CO2 are yet to be addressed. Inspired by the natural CaO‐CaCO3 cycle, we herein introduce CaO into electrolysis of SnO2 in affordable molten CaCl2‐NaCl to establish an in situ capture and conversion of CO2. In situ capture of anodic CO2 from graphite anode by the added CaO generates CaCO3. The consequent co‐electrolysis of SnO2 and CaCO3 confines Sn in carbon nanotube (Sn@CNT) in cathode and increases current efficiency of O2 evolution in graphite anode to 71.9 %. The intermediated CaC2 is verified as the nuclei to direct a self‐template generation of CNT, ensuring a CO2‐CNT current efficiency and energy efficiency of 85.1 % and 44.8 %, respectively. The Sn@CNT integrates confined responses of Sn cores to external electrochemical or thermal stimuli with robust CNT sheaths, resulting in excellent Li storage performance and intriguing application as nanothermometer. The versatility of the molten salt electrolysis of CO2 in Ca‐based molten salts for template‐free generation of advanced carbon materials is evidenced by the successful generation of pure CNT, Zn@CNT and Fe@CNT.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Subject
General Chemistry,Catalysis
Cited by
13 articles.
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