材料科学
阳极
锂(药物)
复合数
量子点
锡
纳米复合材料
硒化物
退火(玻璃)
化学工程
电化学
纳米结构
纳米颗粒
热分解
电流密度
纳米技术
复合材料
电极
冶金
物理
物理化学
量子力学
有机化学
化学
医学
硒
内分泌学
工程类
作者
Zhi Xiang Huang,Bo Liu,Dezhi Kong,Ye Wang,Hui Ying Yang
标识
DOI:10.1016/j.ensm.2017.08.008
摘要
Abstract There have been limited applications in Tin Selenide based anode materials for lithium ion batteries due to low capacities from the alloying process (SnSe: 596 mAh g−1, SnSe2: 426 mAh g−1). This is mainly due to the significant loss of capacity during initial conversion process with the formation of Li2Se; a process that is considered irreversible in Tin based (SnXn, X = O, S, Se, n = 1 or 2) anode materials. Herein, ultra-fine Quantum Dots (QDs) of SnSe2 were designed to be embedded in a 3D matrix of rGO to release Sn nanoparticles that are able to catalyze the decomposition Li2Se and drive the conversion of Sn to SnSe2. In this manner, both conversion and alloying reactions can be utilized that greatly increases the effective capacity of SnSe2 anode. Through facile solvothermal synthesis followed by freeze-drying and thermal annealing, the rationally designed SnSe2 QDs/rGO effectively promoted reversible conversion of Sn to SnSe2. As a result, the nanocomposite exhibited enhanced capacities (778.5 mAh g−1 at current density of 50 mA g−1) that are beyond its theoretical values. The designed nanostructure also endowed the nanocomposite with high rate capabilities (324.5 mAh g−1 at current density of 5000 mA g−1) and ultra-long cycle life (92.2% capacity retention after 3000 cycles at 2000 mA g−1). Post cycling analysis through ex situ TEM and XRD, coupled with electrochemical studies, were carried out to verify the reversible conversion reactions in SnSe2 QDs/rGO. The successful utilization of both conversion and alloying reactions in SnSe2 enables Tin Selenides to be on par with its oxide and sulfide analogues and hence a potential anode towards high energy density lithium ion batteries.
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