4.7 Article

Synthesis of nickel sulfide-supported on porous carbon from a natural seaweed-derived polysaccharide for high-performance supercapacitors

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 853, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2020.157123

关键词

NiSx@C; Ni-SA; Vulcanization; Supercapacitor

资金

  1. National Natural Science Foundation of China [21676039, 21776026]
  2. Liaoning Revitalization Talents Program [XLYC1902037]
  3. Dalian Leading Talents Project [2018-192]
  4. National Key R&D Program of China [2017YFB0308701]
  5. State Key Laboratory of Bio-Fibers and Eco-Textiles [2017kfkt12]
  6. Opening Project of Guangxi Key Laboratory of Clean Pulp & Papermaking and Pollution Control [2019KF11]
  7. National College Students Innovation and Entrepreneurship Training Program [201910152041]

向作者/读者索取更多资源

Transition metal sulfides, such as NiSx@C hybrids, were successfully synthesized through crosslinking sodium alginate with nickel ions and subsequent high-temperature carbonization and low-temperature vulcanization processes. The comparative electrochemical performances of NiS@C and NiS2@C electrodes were evaluated, with NiS@C showing higher specific capacity and better cycling stability. Additionally, asymmetric supercapacitors composed of the NiSx@C hybrids and active carbon demonstrated excellent energy densities at different power densities.
Transition metal sulfides are regarded as an attractive electrode material because of their excellent metalloid characteristic and good electrical conductivity for supercapacitor applications. Herein, we successfully fabricated a hybrid material of NiSx nanoparticle-supported on porous carbon (NiSx@C) by crosslinking sodium alginate with nickel ions, followed by performing a high-temperature carbonization and low-temperature vulcanization process. The NiS@C and NiS2@C hybrids are obtained through changing the carbonization temperature and adjusting the mass of the S-containing precursor. Both of them are subsequently evaluated for their comparative electrochemical performances. The NiS@C electrode shows an excellent specific capacity of 372.6 mA h g(-1) at 0.5 A g(-1) with a mass loading of 3.5 mg cm(-2), and then retains 216.2 mA h g(-1) even if the current density adds up to 10 A g(-1). In contrast, the NiS2@C electrode delivers a specific capacity of 213.3 mA h g(-1) at 0.5 A g(-1) and an impressive capacity retention rate of 60.7% after 5000 charge-discharge cycles. Besides, the asymmetric supercapacitors composed of the NiSx@C hybrids and active carbon (AC) as the positive and negative electrodes deliver excellent energy densities of 58.7 W h kg(-1) at a power density of 406.4 W kg(-1) (NiS@C//AC device) and 44.4 W h kg(-1) at a power density of 397.6 W kg(-1) (NiS2@C//AC device), respectively. (c) 2020 Elsevier B.V. All rights reserved.

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