假电容
层状双氢氧化物
超级电容器
结晶度
化学工程
镍
材料科学
试剂
电容
电极
碳纤维
无机化学
化学
复合数
冶金
复合材料
有机化学
氢氧化物
物理化学
工程类
作者
Wen Zhang,Hefei Fan,Qianfeng Liu,Na Ta,Yuguang Pu,Xize Chen,Yanwei Sui,Erdong Wang,Peng Cao
标识
DOI:10.1016/j.electacta.2021.139167
摘要
Hydrangea-like hollow carbon shell-supported NiCo LDHs ([email protected] LDHs) have been readily synthesized via a chemical co-precipitation process without extra alkaline reagent added. Different molar ratios of Ni/Co (1:4, 2:3, 3:2 and 4:1) in the initial reactants were applied to explore its effect on a series of as-synthesized electrode materials. The optimized [email protected] LDHs with an actual Ni/Co molar ratio of ∼4.8:1 (reactant ratio of 4:1) exhibited the highest specific capacity of 758 C g−1 at 2 A g−1 and displayed excellent rate performance with 79% capacity retention at 20 A g−1. The much improved supercapacitive performance results from the high Ni concentration, which has induced the uniform growth and intimate contact of NiCo LDHs with weak crystallinity on hollow carbon shells to form a hydrangea-like structure. This unique structure and crystalline phase exposes more active sites and facilitates faster ion diffusion. Meanwhile, the Ni-rich NiCo LDHs increases divalent metal cations to achieve high pseudocapacitance. In addition, the assembled [email protected] LDHs//AC asymmetrical supercapacitor maintains 70% capacitance after 4000 cycles and possesses rapid electrokinetics.
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