过电位
碲
阴极
电池(电)
氧化还原
锌
电化学
掺杂剂
电解质
化学工程
储能
材料科学
化学
纳米技术
冶金
电极
光电子学
兴奋剂
物理
功率(物理)
量子力学
物理化学
工程类
作者
Yue Zhang,Amardeep Amardeep,Zhenrui Wu,Li Tao,Jia Xu,Donald J. Freschi,Jian Liu
标识
DOI:10.1002/advs.202308580
摘要
Abstract Aqueous rechargeable zinc‐sulfur (Zn‐S) batteries are a promising, cost‐effective, and high‐capacity energy storage technology. Still, they are challenged by the poor reversibility of S cathodes, sluggish redox kinetics, low S utilization, and unsatisfactory areal capacity. This work develops a facile strategy to achieve an appealing high‐areal‐capacity (above 5 mAh cm −2 ) Zn‐S battery by molecular‐level regulation between S and high‐electrical‐conductivity tellurium (Te). The incorporation of Te as a dopant allows for manipulation of the Zn‐S electrochemistry, resulting in accelerated redox conversion, and enhanced S utilization. Meanwhile, accompanied by the S‐ZnS conversion, Te is converted to zinc telluride during the discharge process, as revealed by ex‐situ characterizations. This additional redox reaction contributes to the S cathode's total excellent discharge capacity. With this unique cathode structure design, the carbon‐confined TeS cathode (denoted as Te 1 S 7 /C) delivers a high reversible capacity of 1335.0 mAh g −1 at 0.1 A g −1 with a mass loading of 4.22 mg cm −2 , corresponding to a remarkable areal capacity of 5.64 mAh cm −2 . Notably, a hybrid electrolyte design uplifts discharge plateau, reduces overpotential, suppresses Zn dendrites growth, and extends the calendar life of Zn‐Te 1 S 7 batteries. This study provides a rational S cathode structure to realize high‐capacity Zn‐S batteries for practical applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI