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用于高性能混合超级电容器的硫化镍的配位剂主导相控制

Coordination agent-dominated phase control of nickel sulfide for high-performance hybrid supercapacitor.

作者信息

Hu Qin, Zhang Shengtao, Zou Xuefeng, Hao Jiangyu, Bai Youcun, Yan Lijin, Li Wenpo

机构信息

Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China.

Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044, China.

出版信息

J Colloid Interface Sci. 2022 Feb;607(Pt 1):45-52. doi: 10.1016/j.jcis.2021.08.185. Epub 2021 Aug 31.

Abstract

The property of an active material is not only influenced by its morphology and size, but also by its crystal phase. The present phase regulation of nickel sulfide is mainly achieved by controlling the participation of sulfur source in reaction. Thus, new perspectives direct at phase control need to be explored and supplemented. Herein, we proposed a novel coordination agent-dominated phase modulation strategy assisted by a hydrothermal process. It is found that increasing the amount of coordination agent can drove the phase transformation from the initial composite of β-NiS/α-NiS/NiS to β-NiS/α-NiS, and then to pure β-NiS. The mechanism of phase regulation has been proposed, and the general application of this method has been demonstrated. By employing coordination agent, the size of resulted products is reduced, and the morphology is optimized. As a result, all of the pure β-NiS electrodes indicate significantly enhanced specific capacity than the pristine β-NiS/α-NiS/NiS composite. Notably, the sample synthesized with 3 mmol of urea (S11) shows uniform morphology and smallest size, and it gives a highest specific capacity of 223.8 mAh g at 1 A g, almost 1.5 times of the original sample. The fabricated S11//rGO device delivers a high energy density of 56.6 Wh·kg at a power density of 407.5 W·kg, and keeps an impressive capacity retention of 84% after 20,000 cycles. This work put forwards a new prospect for controlling the phase and composition of nickel sulfide based on coordination chemistry.

摘要

活性材料的性能不仅受其形态和尺寸的影响,还受其晶相的影响。目前硫化镍的相调控主要通过控制硫源在反应中的参与来实现。因此,需要探索和补充针对相控制的新视角。在此,我们提出了一种由新型配位剂主导的相调制策略,并辅以水热过程。研究发现,增加配位剂的用量可促使相从初始的β-NiS/α-NiS/NiS复合物转变为β-NiS/α-NiS,进而转变为纯β-NiS。提出了相调控的机制,并证明了该方法的普遍适用性。通过使用配位剂,所得产物的尺寸减小,形态得到优化。结果,所有纯β-NiS电极的比容量均比原始的β-NiS/α-NiS/NiS复合物显著提高。值得注意的是,用3 mmol尿素合成的样品(S11)具有均匀的形态和最小的尺寸,在1 A g下具有223.8 mAh g的最高比容量,几乎是原始样品的1.5倍。制备的S11//rGO器件在407.5 W·kg的功率密度下具有56.6 Wh·kg的高能量密度,并且在20,000次循环后保持令人印象深刻的84%的容量保持率。这项工作基于配位化学为控制硫化镍的相和组成提出了新的前景。

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