阴极
水溶液
材料科学
化学工程
锌
储能
电导率
氧化还原
聚合物
纳米技术
无机化学
化学
复合材料
有机化学
冶金
物理化学
工程类
功率(物理)
物理
量子力学
作者
Mingchang Zhu,Qiuying Gao,Mengxian Zheng,Lei Wang,Ya‐Guang Sun,Jingwei Liu,Shuangyan Wu
标识
DOI:10.1021/acssuschemeng.4c06725
摘要
Aqueous zinc-ion batteries (AZIBs) as a new generation of environmentally friendly, high-security, and low-cost energy storage devices have received extensive attention from researchers. Coordination polymers (CPs) show great potential as cathode materials for AZIBs due to their tunable composition, diverse functional groups, highly ordered porous channels, and easily controllable structure. Nevertheless, the inherent limitations of CPs including poor electrical conductivity and low chemical stability severely constrain the cycling stability and rate property of AZIBs. Herein, a highly crystalline calcium-based CP (Ca-ddmb/Ca2L(H2O)2) with a 2D-layered structure was directly successfully grown on nanocarbon black via a simple solvothermal method. The resulting Ca-ddmb@C composite with high electrical conductivity was designed as a cathode to construct high-performance AZIBs. Profiting from the synergistic effect of abundant active sites of Ca-ddmb and conductive nanocarbon, Ca-ddmb@C exhibited a high reversible capacity of 346.75 mAh g–1 at 100 mA g–1 and demonstrated a superb rate performance of 53.34 mAh g–1 at 2000 mA g–1. An in-depth study of the zinc storage mechanism through a series of characterization techniques revealed the redox-active sites of Ca-ddmb. This study provides new insights into the design of a desirable-performance CP-based cathode for AZIBs.
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