过电位
催化作用
材料科学
电池(电)
分解
石墨烯
氧化物
电化学
化学工程
锂(药物)
储能
纳米技术
电极
化学
冶金
物理化学
有机化学
工程类
医学
功率(物理)
物理
量子力学
内分泌学
作者
Lijiao Zhou,Hui Wang,Kun Zhang,Yaqin Qi,Chao Shen,Ting Jin,Keyu Xie
标识
DOI:10.1007/s40843-020-1638-6
摘要
Lithium carbon dioxide (Li-CO2) batteries deliver a theoretical energy density of 1876 W h kg−1 in terms of effective utilization of greenhouse gases. This battery system is considered to be an encouraging electrochemical energy storage device and a promising alternative to Li-ion batteries. However, the main drawback of Li-CO2 batteries is their accumulative discharge product of Li2CO3/C, which leads to large overpotential and poor cycling performance. Thus, specific and efficient catalysts must be explored to enhance the decomposition of Li2CO3/C. Single-atom catalysts (SACs) are regarded as promising heterogeneous catalysts owing to their maximized utilization of metal atoms and strong interfacial electronic interactions. Herein, single-metal atoms of Fe, Co, and Ni uniformly anchored on N-doped reduced graphene oxide (rGO), designated as Fe1/N-rGO, Co1/N-rGO, and Ni1/N-rGO, respectively, are designed and fabricated to investigate their catalytic activity toward the decomposition of Li2CO3/C. Among them, Fe1/N-rGO delivers a high discharge capacity of 16,835 mA h g−1 at 100 mA g−1 and maintains stability for more than 170 cycles with a discharge voltage of 2.30 V at 400 mA g−1. Therefore, this catalysts are overwhelmingly superior to other types. This work reveals the advances of SACs in Li-CO2 batteries and offers an effective method for realizing high-performance Li-CO2 batteries.
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