Lan Wang, Qianqiao Wang, Jianming Li, Xiaoliang Wu, Xiaobin Fan
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Furthermore, the heterostructure between CoNiP and CoNiSe optimizes the electronic structure of the host material, facilitating OH<sup>–</sup> adsorption and desorption, accelerating electron transfer and enhancing the efficiency of redox processes. Benefiting from the structural advantages and synergistic effects, the obtained CoNiP@CoNiSe electrode showcases a high specific capacity of 931 C g<sup>–1</sup>, an ultrafast rate capacity (652 C g<sup>–1</sup> at 30 A g<sup>–1</sup>, 70% retention) and outstanding long-term cycling durability, with a capacity retention of 83% after 10,000 cycles. Beyond that, when configured in an asymmetric supercapacitor setup as CoNiP@CoNiSe//AC, it attains a notable energy density of 47.3 W h kg<sup>–1</sup>, coupled with a robust power density of 266.7 W kg<sup>–1</sup>. Moreover, the configuration maintains an impressive 78% of its capacitance even after enduring 10,000 cycles. 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引用次数: 0
摘要
过渡金属磷化物和硒化物在推进储能技术方面具有巨大的前景。然而,缓慢的反应动力学和有限的速率性能是大规模储能的主要挑战。本文采用高度可调的金属有机框架(MOF)模板,通过纳米结构和异质结构相结合的策略来设计CoNiP@CoNiSe。纳米片结构可以实现快速的电子和离子传输,同时提供丰富的电活性位点,从而提高电导率和比容量。此外,CoNiP和CoNiSe之间的异质结构优化了宿主材料的电子结构,促进了OH -的吸附和解吸,加速了电子转移,提高了氧化还原过程的效率。得益于结构优势和协同效应,获得的CoNiP@CoNiSe电极具有931 C g-1的高比容量,超快的倍率容量(30 a g-1时652 C g-1,保留率70%)和出色的长期循环耐久性,在10,000次循环后容量保留率为83%。除此之外,当配置在不对称超级电容器设置为CoNiP@CoNiSe//AC时,它可以获得47.3 W h kg-1的显著能量密度,以及266.7 W kg-1的强大功率密度。此外,即使在经历10,000次循环后,该配置仍能保持78%的电容。这种异质结构构建的创新方法为提高过渡金属基电极在超级电容器中的电化学性能提供了有价值的蓝图。
Metal Organic Framework Derived Heterogeneous CoNiP@CoNiSe for High Performance Asymmetric Supercapacitor
Transition metal phosphides and selenides hold immense promise for advancing energy storage technologies. However, sluggish reaction kinetics and limited rate performance present major challenges to large-scale energy storage. Herein, a highly tunable metal–organic framework (MOF) template was employed to design CoNiP@CoNiSe through a strategy that integrates both nanostructures and heterostructures. The nanosheet structure enables rapid electron and ion transport while providing abundant electroactive sites, which in turn improves electrical conductivity and specific capacity. Furthermore, the heterostructure between CoNiP and CoNiSe optimizes the electronic structure of the host material, facilitating OH– adsorption and desorption, accelerating electron transfer and enhancing the efficiency of redox processes. Benefiting from the structural advantages and synergistic effects, the obtained CoNiP@CoNiSe electrode showcases a high specific capacity of 931 C g–1, an ultrafast rate capacity (652 C g–1 at 30 A g–1, 70% retention) and outstanding long-term cycling durability, with a capacity retention of 83% after 10,000 cycles. Beyond that, when configured in an asymmetric supercapacitor setup as CoNiP@CoNiSe//AC, it attains a notable energy density of 47.3 W h kg–1, coupled with a robust power density of 266.7 W kg–1. Moreover, the configuration maintains an impressive 78% of its capacitance even after enduring 10,000 cycles. This innovative approach to heterostructure construction offers a valuable blueprint for elevating the electrochemical performance of transition metal-based electrodes in supercapacitor applications.
期刊介绍:
ndustrial & Engineering Chemistry, with variations in title and format, has been published since 1909 by the American Chemical Society. Industrial & Engineering Chemistry Research is a weekly publication that reports industrial and academic research in the broad fields of applied chemistry and chemical engineering with special focus on fundamentals, processes, and products.