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新型基于 MOFs 的钴和多孔石墨碳硫主体材料用于高性能锂硫电池。

Novel Sulfur Host Composed of Cobalt and Porous Graphitic Carbon Derived from MOFs for the High-Performance Li-S Battery.

机构信息

College of Chemistry and Materials Science , Anhui Normal University , Wuhu 241000 , P. R. China.

PSL Research University, Chimie ParisTech-CNRS , Institut de Recherche de Chimie Paris (IRCP) , 11 rue Pierre et Marie Curie , Paris 75005 , France.

出版信息

ACS Appl Mater Interfaces. 2018 Apr 25;10(16):13499-13508. doi: 10.1021/acsami.8b00915. Epub 2018 Apr 11.

Abstract

A composite consisting of cobalt and graphitic porous carbon (Co@GC-PC) is synthesized from bimetallic metal-organic frameworks and employed as the sulfur host for high-performance Li-S batteries. Because of the presence of a large surface area (724 m g) and an abundance of macro-/mesopores, the Co@GC-PC electrode is able to alleviate the debilitating effect originating from the volume expansion/contraction of sulfur species during the cycling process. Our in situ UV/vis analysis indicates that the existence of Co@GC-PC promotes the adsorption of polysulfides during the discharge process. Density functional theory calculations show a strong interaction between Co and LiS and a low decomposition barrier of LiS on Co(111), which is beneficial to the following LiS oxidation in the charge process. As a result, at 0.2C, the discharge capacity of the S/Co@GC-PC cathode is stabilized at 790 mAh g after 220 cycles, much higher than that of a carbon-based cathode, which delivers a discharge capacity of 188 mAh g.

摘要

一种由钴和石墨多孔碳(Co@GC-PC)组成的复合材料是由双金属金属有机骨架合成的,并被用作高性能 Li-S 电池的硫主体。由于具有大的表面积(724 m g)和丰富的大/介孔,Co@GC-PC 电极能够缓解在循环过程中硫物种的体积膨胀/收缩引起的有害影响。我们的原位 UV/vis 分析表明,Co@GC-PC 的存在促进了多硫化物在放电过程中的吸附。密度泛函理论计算表明,Co 和 LiS 之间存在强烈的相互作用,LiS 在 Co(111)上的分解势垒较低,这有利于在充电过程中随后的 LiS 氧化。结果,在 0.2C 下,S/Co@GC-PC 正极在 220 次循环后稳定在 790 mAh g 的放电容量,远高于基于碳的正极的 188 mAh g 的放电容量。

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