催化作用
材料科学
电化学
电极
过渡金属
Atom(片上系统)
硫黄
金属
电池(电)
纳米技术
化学工程
阴极
物理化学
化学
有机化学
冶金
嵌入式系统
功率(物理)
工程类
物理
量子力学
计算机科学
作者
Zhiyuan Han,Shiyong Zhao,Jiewen Xiao,Xiongwei Zhong,Jinzhi Sheng,Wei Lv,Qianfan Zhang,Guangmin Zhou,Hui‐Ming Cheng
标识
DOI:10.1002/adma.202105947
摘要
Abstract Single‐atom metal catalysts (SACs) are used as sulfur cathode additives to promote battery performance, although the material selection and mechanism that govern the catalytic activity remain unclear. It is shown that d‐p orbital hybridization between the single‐atom metal and the sulfur species can be used as a descriptor for understanding the catalytic activity of SACs in Li–S batteries. Transition metals with a lower atomic number are found, like Ti, to have fewer filled anti‐bonding states, which effectively bind lithium polysulfides (LiPSs) and catalyze their electrochemical reaction. A series of single‐atom metal catalysts (Me = Mn, Cu, Cr, Ti) embedded in three‐dimensional (3D) electrodes are prepared by a controllable nitrogen coordination approach. Among them, the single‐atom Ti‐embedded electrode has the lowest electrochemical barrier to LiPSs reduction/Li 2 S oxidation and the highest catalytic activity, matching well with the theoretical calculations. By virtue of the highly active catalytic center of single‐atom Ti on the conductive transport network, high sulfur utilization is achieved with a low catalyst loading (1 wt.%) and a high area‐sulfur loading (8 mg cm −2 ). With good mechanical stability for bending, these 3D electrodes are suitable for fabricating bendable/foldable Li–S batteries for wearable electronics.
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