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在硫化钴纳米薄片上引导氮掺杂五氧化二钒纳米团簇作为稳定的无缝界面阳极,用于高能量密度和耐用的不对称超级电容器。

Guiding nitrogen doped vanadium pentoxide nanoclusters on cobalt sulfide nano-flakiness as stable seamless interface anode toward highly energy density and durable asymmetric supercapacitors.

作者信息

Zhou Weitong, Jiang Junjie, Li Woyuan, Huang Zhiye, Zhang Mingmei, Jin Jiayang, Yu Zhihao, Xie Jimin

机构信息

School of Chemistry and Chemical Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.

School of Chemistry and Chemical Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.

出版信息

J Colloid Interface Sci. 2025 Feb;679(Pt A):531-543. doi: 10.1016/j.jcis.2024.10.001. Epub 2024 Oct 2.

Abstract

Interaction of the interface-heterostructures is crucial to rapid ionic conductivity and highly energy density of electrode materials toward supercapacitors. Herein, a novel anode heterostructure is synthesized using cobalt sulfide (CoS) nanoflowers as a substrate for composite nitrogen doped vanadium pentoxide (denoted as N-VO@CoS) by combination of hydrothermal and calcination method. As expected, the N-VO@CoS electrode possesses superhigh specific surface area that significantly enhances the specific capacitance, and its unique porous interconnected structure not only reduces the volume effect during the cycles, but also greatly enhances the conductivity of electron transfer. The as-prepared N-VO@CoS electrode has a specific capacitance of up to 2413.6F/g at a current density of 1 A/g, and can still maintain 87.51 % of the initial capacitance after 5,000 cycles at a high current density of 10 A/g. More importantly, the partial density of states (PDOS) ares obtained through theoretical calculations reveal that the interaction of heterogeneous interfaces is contributed by the p-orbitals of C, O and S and d-orbitals of V and Co. In addition, asymmetric supercapacitor (ASC) with N-VO@CoS as the positive electrode and activated carbon (AC) as the negative electrode has a high voltage of 1.7 V, which achieves an outstanding energy density of 71.6 W h kg at a power density of 849.8 W kg, showing excellent cycle stability (retain 90.6 % of the initial capacitance after 10,000 charge/discharge cycles). This paper offers novel paradigm for the doping of metal oxides and the development of heterostructures, which provides support for their use as advanced energy storage materials.

摘要

界面异质结构的相互作用对于超级电容器电极材料的快速离子传导性和高能量密度至关重要。在此,通过水热法和煅烧法相结合,以硫化钴(CoS)纳米花为基底合成了一种新型阳极异质结构,用于复合氮掺杂五氧化二钒(记为N-VO@CoS)。正如预期的那样,N-VO@CoS电极具有超高的比表面积,显著提高了比电容,其独特的多孔互连结构不仅减少了循环过程中的体积效应,还大大提高了电子转移的导电性。所制备的N-VO@CoS电极在1 A/g的电流密度下比电容高达2413.6F/g,在10 A/g的高电流密度下经过5000次循环后仍能保持初始电容的87.51%。更重要的是,通过理论计算得到的部分态密度(PDOS)表明,异质界面的相互作用是由C、O和S的p轨道以及V和Co的d轨道贡献的。此外,以N-VO@CoS为正极、活性炭(AC)为负极的不对称超级电容器(ASC)具有1.7 V的高电压,在849.8 W kg的功率密度下实现了71.6 W h kg的出色能量密度,显示出优异的循环稳定性(在10000次充放电循环后保留初始电容的90.6%)。本文为金属氧化物的掺杂和异质结构的开发提供了新的范例,为其作为先进储能材料的应用提供了支持。

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