材料科学
微型反应器
催化作用
纳米线
多硫化物
阴极
锂(药物)
法拉第效率
镍
锂硫电池
电池(电)
钴
纳米技术
化学工程
电化学
电极
物理化学
电解质
冶金
内分泌学
功率(物理)
工程类
化学
物理
医学
量子力学
生物化学
作者
Zihan Shen,Mengqiu Cao,Zili Zhang,Jun Pu,Chenglin Zhong,Jiachen Li,Haixia Ma,Fujun Li,Jia Zhu,Feng Pan,Huigang Zhang
标识
DOI:10.1002/adfm.201906661
摘要
Abstract High‐loading lithium–sulfur (Li–S) batteries suffer from poor electrochemical properties. Electrocatalysts can accelerate polysulfides conversion and suppress their migration to improve battery cyclability. However, catalysts for Li–S batteries usually lack a rational design. A d‐band tuning strategy is reported by alloying cobalt to metal sites of Ni 2 P to enhance the interaction between polysulfides and catalysts. A molecular or atomic level analysis reveals that Ni 2 Co 4 P 3 is able to weaken the SS bonds and lower the activation energy of polysulfides conversion, which is confirmed with temperature‐dependent experiments. Ni 2 Co 4 P 3 nanowires are further fabricated on a porous nickel scaffold to unfold the catalytic activity by its large surface area. Using a simple ion‐selective filtration shell, a microreactor‐like S cathode (MLSC) is constructed to realize ultrahigh S loading (25 mg cm −2 ). As such, a microreactor design integrates reaction and separation in one cell and can effectively address the polysulfide issues, the MLSC cell demonstrates excellent properties of cyclability and high capacity (1223 mAh g −1 at 0.1 C). More importantly, the catalyst's designs and microreactor strategies provide new approaches for addressing the complicated issues of Li–S batteries.
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