材料科学
阴极
储能
稳健性(进化)
纳米尺度
电容
电导率
电极
光电子学
化学工程
纳米技术
复合材料
功率(物理)
电气工程
生物化学
量子力学
基因
物理
工程类
物理化学
化学
作者
Lanxin Xue,Li Zeng,Wenbin Kang,Haiyan Chen,Yin Hu,Yaoyao Li,Wei Chen,Tianyu Lei,Yichao Yan,Chengtao Yang,Anjun Hu,Xianfu Wang,Jie Xiong,Chuhong Zhang
标识
DOI:10.1002/aenm.202100420
摘要
Abstract Holding manifold advantages including environmental benignity, enhanced structural robustness, and high capacity, Li 2 S as a competitive substitute of sulfur in Li–S batteries is receiving escalating attention. However, serious issues rooted in its intrinsic poor conductivity and sluggish mass transport present the significant challenge of achieving high active material use with appealing kinetics for effective scaling in areal capacitance under elevated loading densities. This renders current Li 2 S cathodes incapable of securing energy availability that responds to power‐hungry modern electronics. Here for the first time, an interfacial engineering approach is devised by in situ decorating a 3D printed carbonaceous scaffold with uniform surface‐deposited Li 2 S and by healing the printed adjacent interface to eliminate the interfacial resistance. As a result, facile mass transport throughout the whole printed matrix is enabled. 3D printed electrodes with high active material use and loading‐insensitive performance delivering outstanding areal capacity and fast kinetics of 6.29 mAh cm −2 at 6 mA cm −2 under an impressive loading density of 10 mg cm −2 are realized, which are among the best results reported for Li 2 S‐based batteries. The thrilling performance points to a highly effective approach that advances the performance of Li 2 S cathodes closer toward real‐world applications.
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