超级电容器
电容
层状结构
化学
位阻效应
电化学
聚合物
极化率
假电容器
储能
化学工程
功率密度
钴
纳米技术
假电容
配位聚合物
双层电容
Crystal(编程语言)
表面能
化学物理
晶体生长
电极
调制(音乐)
作者
Zhao-ting Shang,Yi Xie,Dandan Chen,Wangting Lu,Fan Yu,Xiaolun Peng
标识
DOI:10.1021/acs.inorgchem.5c03384
摘要
Supercapacitors are promising energy storage device due to their rapid charge/discharge, high power density and long cycle life. Two-dimensional (2D) Coordination Polymers (CPs) exhibit significant potential for electrochemical energy storage. However, controlling the morphology of 2D CPs remains challenging. Controlling the morphology of 2D CPs remains challenging. In this study, pseudohalide anions (SeCN–, SCN–) were employed as crystal growth modifiers to achieve precise morphological control, leveraging their distinct coordination capacities and steric hindrance effects. Specifically, the large atomic radius and high polarizability of Se in SeCN– facilitate the lateral growth of CPs, leading to the formation of uniform lamellar structures. Co-CP-Se delivered a specific capacitance of 1483 F g–1 at 1 A g–1 and maintained 93.23% of its initial capacitance after 5000 cycles at 10 A g–1. A hybrid supercapacitor (Co-CP-Se//AC) demonstrated a power density of 750 W kg–1 at an energy density of 42.14 Wh kg–1 while maintaining 90.12% capacitance retention after 5000 cycles (10 A g–1). Mechanistic investigations revealed that partial substitution of −SeCN by OH– during cycling generated Co(OH)2, which synergistically contributed to the capacitance together with Co-CP-Se. The uniform lamellar architecture optimized the electrolyte-electrode interface contact and offered critical insights for the structural design of 2D CPs toward high-performance energy storage applications.
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