氧化还原
纳米团簇
材料科学
电化学
碳纤维
化学工程
多金属氧酸盐
催化作用
硫黄
石墨烯
氧化物
锂(药物)
煅烧
阴极
溶解
无机化学
基质(水族馆)
纳米技术
储能
电极
动力学
多硫化物
半反应
电导率
电催化剂
电化学能量转换
电化学动力学
化学
纳米颗粒
作者
Jin‐Hua Liu,Yuan‐Qing Dong,Ming‐Yue Yu,Hao Liu,Shulin Song,Yanfang Huo,Yanqing Wang,WR Li
摘要
ABSTRACT Lithium–sulfur batteries (LSBs) have emerged as one of the most prospective next‐generation rechargeable energy storage devices because of their exceptional energy densities. However, the dissolution and shuttle behavior of lithium polysulfides (LiPSs) intermediates, coupled with slow redox dynamics, have impeded their practical application. In this respect, polyoxometalates (POMs) represent a class of metal‐oxide nanoclusters capable of reversible multielectron redox and efficient LiPSs capture, which enable them to maintain the reversibility of LiPSs conversion while accelerating the redox kinetics of LiPSs. However, the poor conductivity of POMs restricts their electrochemical performance in LSBs with high sulfur loading. To address this issue, the nano‐porous K 3 PW 12 O 40 ( KPW ) is in situ grown on three‐dimensional (3D) carbon cloth@reduced graphene oxide ( CC@RGO ) conductive substrate to gain a POM‐based host material ( CC@RGO/KPW‐A ) as catalyst via the two‐step calcination strategy. This integrated architecture synergistically accelerates the redox kinetics of LiPSs and promotes rapid charge transfer in LSBs, thus significantly improving the performance. The obtained POM‐based sulfur cathode shows an initial discharge capacity of 9.6 mAh cm −2 even under a high sulfur loading of 10.2 mg cm −2 . This work provides a facile approach to boost the electrochemical properties of LSBs with high sulfur loading.
科研通智能强力驱动
Strongly Powered by AbleSci AI