Qingli Xu , Qi Zhang , Zhigen Yu , Mengjuan Zhou , Haoyin Zhong , Yuanyuan Li , Ping Wang , Yan Zhang , Wee Siang Vincent Lee , Kun Zhang
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引用次数: 0
Abstract
Molybdenum disulfide (MoS2) is touted as a highly promising material for fiber-shaped supercapacitors (FSCs) but limited by its low capacitance and unsatisfactory cycling stability. Here, we report a MoS2 deposited stainless steel wire (MoS2@SSW) that can be electrochemically intercalated with dual ions (Na+ and H+). A high capacitance of ∼1632.7 mF cm−2 at 0.4 mA cm−2 and high capacitance retention of 84.25 % after 10,000 cycles under sulfuric acid/sodium sulfate (H2SO4/Na2SO4) aqueous electrolyte is recorded for this system. This is mainly attributed to the pre-intercalation of H+ into MoS2 to form MoS-SH. This process redistributes the local charge regions on MoS2 surface and lowers the energy barrier for Na+ migration in MoS2 to facilitate the adsorption and intercalation of Na+. Notably, MoS2@SSW FSCs are integrated into three-dimensional space textiles as a proof-of-concept. This novel exploration of the nanointerface resulted by electrolyte engineering offers a feasible design paradigm for the development of high-performing FSCs.
二硫化钼(MoS2)被认为是一种非常有前途的光纤型超级电容器(FSCs)材料,但其低电容和不理想的循环稳定性受到限制。在这里,我们报道了一种MoS2沉积的不锈钢丝(MoS2@SSW),可以电化学插入双离子(Na+和H+)。在0.4 mA cm - 2下,该系统的高电容值为1632.7 mF cm - 2,在硫酸/硫酸钠(H2SO4/Na2SO4)水溶液电解质下循环10000次后,高电容保持率为84.25%。这主要是由于H+预嵌入到MoS2中形成了MoS-SH。这一过程重新分配了MoS2表面的局部电荷区,降低了Na+在MoS2中迁移的能垒,有利于Na+的吸附和插层。值得注意的是,MoS2@SSW FSCs作为概念验证被集成到三维空间纺织品中。电解质工程对纳米界面的新探索为高性能FSCs的开发提供了可行的设计范例。
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies