Targeted Synergy between Adjacent Co Atoms on Graphene Oxide as an Efficient New Electrocatalyst for Li-CO2 Batteries

被引:104
作者
Zhang, Bin-Wei [1 ,2 ]
Jiao, Yan [1 ]
Chao, Dong-Liang [1 ]
Ye, Chao [1 ]
Wang, Yun-Xiao [2 ]
Davey, Kenneth [1 ]
Liu, Hua-Kun [2 ]
Dou, Shi-Xue [2 ]
Qiao, Shi-Zhang [1 ,3 ]
机构
[1] Univ Adelaide, Sch Chem Engn & Adv Mat, Ctr Mat Energy & Catalysis, Adelaide, SA 5005, Australia
[2] Univ Wollongong, Australian Inst Innovat Mat, Inst Superconducting & Elect Mat, Innovat Campus, North Wollongong, NSW 2500, Australia
[3] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
基金
澳大利亚研究理事会; 中国国家自然科学基金;
关键词
carbon dioxide; cobalt; electrocatalysts; graphene oxide; Li-CO2; batteries; REDUCTION; CATALYSIS; OXIDATION; STRATEGY; CLUSTERS;
D O I
10.1002/adfm.201904206
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Li-CO2 batteries are an attractive technology for converting CO2 into energy. However, the decomposition of insulating Li2CO3 on the cathode during discharge is a barrier to practical application. Here, it is demonstrated that a high loading of single Co atoms (approximate to 5.3%) anchored on graphene oxide (adjacent Co/GO) acts as an efficient and durable electrocatalyst for Li-CO2 batteries. This targeted dispersion of atomic Co provides catalytically adjacent active sites to decompose Li2CO3. The adjacent Co/GO exhibits a highly significant sustained discharge capacity of 17 358 mA h g(-1) at 100 mA g(-1) for >100 cycles. Density functional theory simulations confirm that the adjacent Co electrocatalyst possesses the best performance toward the decomposition of Li2CO3 and maintains metallic-like nature after the adsorption of Li2CO3.
引用
收藏
页数:7
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