多硫化物
磷化物
分离器(采油)
材料科学
电解质
化学工程
镁
铜
多收费
膜
吸附
储能
无机化学
电极
化学
冶金
镍
有机化学
电池(电)
物理化学
功率(物理)
工程类
物理
热力学
量子力学
生物化学
作者
Yang Yang,Wenbin Fu,Duo Zhang,Wen Ren,Shuxin Zhang,Xiaowei Yang,Yu Zhang,Sang‐Jun Lee,Jun‐Sik Lee,Zi‐Feng Ma,Jun Yang,Jiulin Wang,Yanna NuLi
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-12-30
卷期号:17 (2): 1255-1267
被引量:23
标识
DOI:10.1021/acsnano.2c09302
摘要
Magnesium–sulfur (Mg-S) batteries are emerging as a promising alternative to lithium-ion batteries, due to their high energy density and low cost. Unfortunately, current Mg-S batteries typically suffer from the shuttle effect that originates from the dissolution of magnesium polysulfide intermediates, leading to several issues such as rapid capacity fading, large overcharge, severe self-discharge, and potential safety concern. To address these issues, here we harness a copper phosphide (Cu3P) modified separator to realize the adsorption of magnesium polysulfides and catalyzation of the conversion reaction of S and Mg2+ toward stable cycling of Mg-S cells. The bifunctional layer with Cu3P confined in a carbon matrix is coated on a commercial polypropylene membrane to form a porous membrane with high electrolyte wettability and good thermal stability. Density functional theory (DFT) calculations, polysulfide permeability tests, and post-mortem analysis reveal that the catalytic layer can adsorb polysulfides, effectively restraining the shuttle effect and facilitating the reversibility of the Mg-S cells. As a result, the Mg-S cells can achieve a high specific capacity, fast rates (449 mAh g–1 at 0.1 C and 249 mAh g–1 at 1.0 C), and a long cycle life (up to 500 cycles at 0.5 C) and operate even at elevated temperatures.
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