4.6 Article

Controlled sulfurization of MnCO3 microcubes architectured MnS2 nanoparticles with 1.7 fold capacitance increment for high energy density supercapacitor

Journal

ELECTROCHIMICA ACTA
Volume 301, Issue -, Pages 366-376

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2019.01.185

Keywords

MnCO3 microcubes; MnS2 nanoparticles; Sulfurization; Supercapacitor; Thin film

Funding

  1. Department of Science and Technology-Science and Engineering Research Board (DST-SERB), New Delhi India [SERB/F/7448/2016-17]
  2. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2017R1E1A1A01074550]
  3. National Research Foundation of Korea [2017R1E1A1A01074550] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Recently, sulfurization and phosphorylation protocols are employed in porous nano-materials preparation beneficial to improve energy density and power density of pseudocapacitors. Due to well-defined redox activity and higher theoretical capacitance, manganese sulfide electrode is used in super-capacitor application. In present work, MnCO3 microcubes are converted into MnS2 nanoparticles using cost-effective high diffusion rate sulfurization method. Reducing size of material from microcubes to nanoparticles has facilitated rate capability in the material along with improved capacitance. MnS2 nanoparticles exhibit 713 Fg(-1) specific capacitance at 5 mVs(-1) scan rate compared with 407 Fg(-1) obtained for MnCO3 microcubes. The impedance study analyzes improvement in interfacial conductivity for MnS2 nanoparticles observed form 1.83 Omega cm(-2) equivalent series resistance in comparison with 2.35 cm(-2) for MnCO3 microcubes. Fabricated solid state MnS2//MoS2 asymmetric supercapacitor exhibits 41.7 Whkg(-1) energy density, and 450 Wkg(-1) power density with the respectable 88 % capacitance retention for the continuous 2000 CV cycles charging and discharging at 100 mVs(-1) scan rate. (C) 2019 Elsevier Ltd. All rights reserved.

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