多硫化物
锡
阴极
氮化钛
X射线光电子能谱
电解质
材料科学
氮化物
电池(电)
溶解
化学工程
锂硫电池
电极
锂(药物)
钛
无机化学
化学
纳米技术
冶金
图层(电子)
医学
功率(物理)
物理
物理化学
量子力学
内分泌学
工程类
作者
Negar Mosavati,Venkateswara Rao Chitturi,Steven O. Salley,K. Y. Simon Ng
标识
DOI:10.1016/j.jpowsour.2016.04.099
摘要
Lithium–sulfur (LiS) batteries could potentially revolutionize the rechargeable battery market due to their high energy density and low cost. However, low active material utilization, electrode volumetric expansion and a high rate of capacity fade due to the dissolution of lithium polysulfide intermediates in the liquid electrolyte are the main challenges facing further LiS battery development. Here, we enhanced LiS batteries active material utilization and decreased the volumetric expansion by using the lithium/dissolved polysulfide configuration. Moreover, a novel class of cathode materials, Titanium Nitride (TiN), was developed for polysulfide conversion reactions. The surface chemical environment of the TiN has been investigated by X-ray photoelectron spectroscopy (XPS) analysis. The existence of STiN bonding at the cathode electrode surface was observed, which indicates the strong interactions between TiN and polysulfides. Therefore, the TiN electrode retains the sulfur species on the cathode surface, minimizing the active material and surface area loss and consequently, improves the capacity retention. The resultant cells demonstrated a high initial capacity of 1524 mAh g−1 and a good capacity retention for 100 cycles at a C/10 current rate.
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