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在微米级碳板上原位构建层间距可调的镍钴层状双氢氧化物纳米分支用于高性能超级电容器。

In situ construction of NiCo-layered double hydroxide nanobranches with adjustable layer spacing on micro-sized carbon plate for high-performance supercapacitors.

作者信息

Lu Zhongqi, Zhao Kai, Duan Lejiao, Sun Huiru, Xu Jiangtao, Marquez Kevinilo P, Zhang Jizhen, Liu Jingquan

机构信息

College of Materials Science and Engineering, Institute for Graphene Applied Technology Innovation, Qingdao University, Qingdao 266071, China.

Institute for Frontier Materials, Deakin University, Geelong, Victoria 3216, Australia; Institute of Chemistry, University of the Philippines-Los Baños, Laguna 4031, Philippines.

出版信息

J Colloid Interface Sci. 2025 Jan 15;678(Pt C):482-493. doi: 10.1016/j.jcis.2024.09.148. Epub 2024 Sep 16.

DOI:10.1016/j.jcis.2024.09.148
PMID:39303566
Abstract

Binary layered double hydroxides (LDHs) are an emerging class of materials for supercapacitors owing to their tunable topological structure and excellent theoretical energy storage capacity. However, aggregation and restacking cause a decrease in the interlayer distance of LDHs, resulting in a considerable drop in real specific capacitance. To address this, large-sized anions are intercalated into the interlayer space. Herein, we constructed 3D top-tangled NiCo-LDH nanobranches in situ on a biomass micro-sized carbon plate (CP). By varying the amount of benzene-1,4-dicarboxylic acid (BDC), we prepared a BDC-intercalated CP/NiCo-LDH composite material with adjustable interlayer spacing. Remarkably, the CP/NiCo-LDH-BDC(0.03) composite exhibited excellent electrochemical properties (1530 F g/212.5 mAh/g at 1 A/g). It retained 88.36 % capacity after 5000 charge-discharge cycles. The constructed CP/NiCo-LDH-BDC(0.03)//CP asymmetric supercapacitor showed excellent gravimetric capacitance (123 F g/54.7 mAh/g at 1 A/g) and energy density (43.7 Wh kg at 800 W kg). Furthermore, two asymmetric capacitors connected in series powered a small lightbulb for 2 min, even in a bent state. These findings show that the fabricated CP and CP/NiCo-LDH-BDC(0.03) electrode materials can be applied in flexible and wearable energy storage systems.

摘要

二元层状双氢氧化物(LDHs)因其可调节的拓扑结构和出色的理论储能容量,成为一类新兴的超级电容器材料。然而,聚集和重新堆叠会导致LDHs层间距减小,从而使实际比电容大幅下降。为了解决这一问题,大尺寸阴离子被插入到层间空间。在此,我们在生物质微尺寸碳板(CP)上原位构建了三维顶部缠结的NiCo-LDH纳米分支。通过改变对苯二甲酸(BDC)的用量,我们制备了一种层间距可调的BDC插层CP/NiCo-LDH复合材料。值得注意的是,CP/NiCo-LDH-BDC(0.03)复合材料表现出优异的电化学性能(在1 A/g时为1530 F g/212.5 mAh/g)。在5000次充放电循环后,它仍保留了88.36%的容量。构建的CP/NiCo-LDH-BDC(0.03)//CP不对称超级电容器表现出优异的重量电容(在1 A/g时为123 F g/54.7 mAh/g)和能量密度(在800 W kg时为43.7 Wh kg)。此外,两个串联的不对称电容器即使在弯曲状态下也能为一个小灯泡供电2分钟。这些发现表明,所制备的CP和CP/NiCo-LDH-BDC(0.03)电极材料可应用于柔性和可穿戴储能系统。

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