硫化
多硫化物
材料科学
化学工程
催化作用
阴极
锂(药物)
异质结
纳米颗粒
纳米技术
硫黄
电极
化学
物理化学
有机化学
光电子学
电解质
冶金
工程类
医学
内分泌学
作者
Fengxing Liang,Qiao Deng,Shunyan Ning,Huibing He,Nannan Wang,Yanqiu Zhu,Jinliang Zhu
标识
DOI:10.1002/advs.202403391
摘要
Abstract The development of lithium–sulfur (Li─S) batteries has been hampered by the shuttling effect of lithium polysulfides (LiPSs). An effective method to address this issue is to use an electrocatalyst to accelerate the catalytic conversion of LiPSs. In this study, heterogeneous MnP‐MnO 2 nanoparticles are uniformly synthesized and embedded in porous carbon (MnP‐MnO 2 /C) as core catalysts to improve the reaction kinetics of LiPSs. In situ characterization and density functional theory (DFT) calculations confirm that the MnP‐MnO 2 heterostructure undergo surface sulfidation during the charge/discharge process, forming the MnS 2 phase. Surface sulfidation of the MnP‐MnO 2 heterostructure catalyst significantly accelerated the SRR and Li 2 S activation, effectively inhibiting the LiPSs shuttling effect. Consequently, the MnP‐MnO 2 /C@S cathode achieves outstanding rate performance (10 C, 500 mAh g −1 ) and ultrahigh cycling stability (0.017% decay rate per cycle for 2000 cycles at 5 C). A pouch cell with MnP‐MnO 2 /C@S cathode delivers a high energy density of 429 Wh kg −1 . This study may provide a new approach to investigating the surface sulfidation of electrocatalysts, which is valuable for advancing high‐energy‐density Li−S batteries.
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