材料科学
纳米片
动力学
电化学
硫黄
氧化还原
电催化剂
化学工程
电化学动力学
碳纤维
扩散
无机化学
纳米技术
电极
复合数
化学
物理化学
复合材料
热力学
物理
工程类
量子力学
冶金
作者
Xin Zhang,Xiangyang Li,Yongzheng Zhang,Xiang Li,Qinghua Guan,Jian Wang,Zechao Zhuang,Quan Zhuang,Xiaomin Cheng,Haitao Liu,Jing Zhang,Chunyin Shen,Hongzhen Lin,Yanli Wang,Liang Zhan,Licheng Ling
标识
DOI:10.1002/adfm.202302624
摘要
Abstract Lithium–sulfur (Li–S) batteries are famous for their high energy density and low cost, but prevented by sluggish redox kinetics of sulfur species due to depressive Li ion diffusion kinetics, especially under low‐temperature environment. Herein, a combined strategy of electrocatalysis and pore sieving effect is put forward to dissociate the Li + solvation structure to stimulate the free Li + diffusion, further improving sulfur redox reaction kinetics. As a protocol, an electrocatalytic porous diffusion‐boosted nitrogen‐doped carbon‐grafted‐CoP nanosheet is designed via forming the NCoP active structure to release more free Li + to react with sulfur species, as fully investigated by electrochemical tests, theoretical simulations and in situ/ex situ characterizations. As a result, the cells with diffusion booster achieve desirable lifespan of 800 cycles at 2 C and excellent rate capability (775 mAh g −1 at 3 C). Impressively, in a condition of high mass loading or low‐temperature environment, the cell with 5.7 mg cm −2 stabilizes an areal capacity of 3.2 mAh cm −2 and the charming capacity of 647 mAh g −1 is obtained under 0 °C after 80 cycles, demonstrating a promising route of providing more free Li ions toward practical high‐energy Li–S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI