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用于锂硫电池的单原子金属嵌入三维电极中的工程d-p轨道杂化

Engineering d-p Orbital Hybridization in Single-Atom Metal-Embedded Three-Dimensional Electrodes for Li-S Batteries.

作者信息

Han Zhiyuan, Zhao Shiyong, Xiao Jiewen, Zhong Xiongwei, Sheng Jinzhi, Lv Wei, Zhang Qianfan, Zhou Guangmin, Cheng Hui-Ming

机构信息

Shenzhen Geim Graphene Center, Tsinghua-Berkeley Shenzhen Institute and Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.

Fuels and Energy Technology Institute and WA School of Mines: Minerals, Energy, and Chemical Engineering, Curtin University, Perth, Western Australia, 6102, Australia.

出版信息

Adv Mater. 2021 Nov;33(44):e2105947. doi: 10.1002/adma.202105947. Epub 2021 Sep 27.

DOI:10.1002/adma.202105947
PMID:34569660
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 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 ). With good mechanical stability for bending, these 3D electrodes are suitable for fabricating bendable/foldable Li-S batteries for wearable electronics.

摘要

单原子金属催化剂(SACs)被用作硫阴极添加剂以提升电池性能,尽管决定催化活性的材料选择和机制仍不明确。研究表明,单原子金属与硫物种之间的d-p轨道杂化可作为理解锂硫电池中SACs催化活性的一个描述符。发现原子序数较低的过渡金属,如Ti,具有较少的满反键态,这能有效结合多硫化锂(LiPSs)并催化其电化学反应。通过可控的氮配位方法制备了一系列嵌入三维(3D)电极的单原子金属催化剂(Me = Mn、Cu、Cr、Ti)。其中,嵌入单原子Ti的电极对LiPSs还原/Li S氧化具有最低的电化学势垒和最高的催化活性,与理论计算结果吻合良好。借助导电传输网络上单原子Ti的高活性催化中心,在低催化剂负载量(1 wt.%)和高面积硫负载量(8 mg cm )的情况下实现了高硫利用率。这些3D电极具有良好的弯曲机械稳定性,适用于制造用于可穿戴电子设备的可弯曲/可折叠锂硫电池。

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