异质结
超级电容器
电解质
材料科学
电容
电化学
电极
纳米技术
化学工程
光电子学
化学
物理化学
工程类
作者
Ying Geng,Siyu Bi,Junyi Zhang,Hui Li,Guojun Dai,Yifan Zhang,Zhengqiang Xia,Qi Yang,Gang Xie,Sanping Chen
标识
DOI:10.1021/acsanm.5c00492
摘要
The rational design of a porous core–shell heterostructure with open spaces is an effective strategy to mitigate the aggregation and volume expansion of active nanoelectrodes during charging/discharging processes. Herein, the leaf-like CoNiSe2/NC@Ni3(PO4)2 core–shell heterostructure with hierarchical pores is in situ grown on activated carbon cloth (CC) as a free-standing electrode for flexible supercapacitors. The open spaces collectively formed by both the interspaces among adjacent leaf-like CoNiSe2/NC@Ni3(PO4)2 structures and the channels among vertically crossed Ni3(PO4)2 nanosheets not only significantly enhance the electrode and electrolyte contact areas to promote rapid electrolyte penetration and ion diffusion but also effectively buffer the agglomeration and volume expansion of the active nanoelectrode. Such unique spatial arrangement and structure endow CoNiSe2/NC@Ni3(PO4)2/CC with a high specific capacitance of 2505 F g–1 (1 A g–1) and an extended cycle life with 91.1% capacity retention after 10,000 cycles, surpassing most reported electrodes with similar compositions. A combined experimental and band structure analysis signifies that the integrated CoNiSe2/Ni3(PO4)2 interfaces featuring an optimized electronic structure accelerate the charge transport and improve the redox-reaction kinetics, resulting in a significant enhancement in electrochemical performance compared to the two individual components.
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