单独一对
电负性
量子点
电化学
吡啶
硫化物
结构稳定性
氧化还原
化学
过渡金属
电子亲和性(数据页)
纳米技术
储能
材料科学
化学物理
电极
分子
无机化学
物理化学
有机化学
工程类
物理
催化作用
功率(物理)
结构工程
量子力学
作者
Wenyong Chen,Xuemei Zhang,Zhaoqian Li,Zhenzhen Feng,Shuanghong Chen,Xianxi Zhang,Yongsheng Zhang,Linhua Hu
标识
DOI:10.1016/j.cej.2019.121981
摘要
The structural collapse of transition metal sulfides in repeated charge and discharge process restricts their cyclic performance. How to effectively remedy stability without sacrifice of capacity still remains a daunting challenge. Herein, ultra-small NiS2 quantum dots (QDs) are assembled with pyridine ligands containing heterocyclic nitrogen atoms of high electronegativity. The induction of electron cloud of heterocyclic nitrogen shortens the NiS bond with stronger structural stability. Besides, the localized lone pair of electrons near nickel atoms reduces the repulsive force to the diffused OH− ions, thus increasing affinity of the redox reaction. Benefiting from the tailor-made of ligands and size effect of QDs, a great promotion in both specific capacity of 651.8 C∙g−1 at 1 A∙g−1 and stability of 94.7% retention at 5 A∙g−1 over 8000 cycles is achieved as compared to ordinary bulk materials. These results demonstrate that ligands induced QDs is a promising strategy for precisely regulating metal sulfide electrode materials of advanced energy storage devices.
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