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Hydroxide ion dependent α-MnO2 enhanced via oxygen vacancies as the negative electrode for high-performance supercapacitors

Manganese dioxide with low-cost and high theoretical capacity plays an essential role in the development of high-performance supercapacitors. However, most of the research on the application of pure MnO2 in supercapacitors is mainly focused on positive electrode materials. In this work, we aim at st...

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Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-02, Vol.9 (5), p.2872-2887
Main Authors: Chen, Yucheng, Zhou, Chengbao, Liu, Gang, Kang, Chenxia, Lin, Ma, Liu, Qiming
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Zhou, Chengbao
Liu, Gang
Kang, Chenxia
Lin, Ma
Liu, Qiming
description Manganese dioxide with low-cost and high theoretical capacity plays an essential role in the development of high-performance supercapacitors. However, most of the research on the application of pure MnO2 in supercapacitors is mainly focused on positive electrode materials. In this work, we aim at studying the applicability and energy storage mechanism of MnO2 as a negative electrode material for supercapacitors, and compared three different crystalline MnO2 (δ-, β-, and α-MnO2). Additionally, the electrochemical performance of α-MnO2 was further improved by introducing oxygen vacancies generated at high temperature. Electrochemical studies show that M-300 (α-MnO2 heat-treated at 300 °C) electrode materials have a high specific capacitance of 736.3 F g−1 at 1 A g−1, and exhibit remarkable cycling stability. Impressively, hydroxide ion dependence experiments and research of the electron transfer mechanism during charge and discharge indicate that the charge storage process of MnO2 as a negative electrode is realized by the participation of OH− and the mutual conversion of Mn(ii), Mn(iii) and Mn(iv), absolutely different from the MnO2 positive electrode. We also theoretically quantified the contribution of the diffusion-controlled process and surface capacitance effects to investigate its energy storage mechanism. The assembled M-300//H-NiCo2O4 asymmetric supercapacitor exhibits excellent energy density (34.9 W h kg−1) and cycling stability (80.6% after 10 000 cycles). This work provides a promising negative electrode material for supercapacitor device fabrication, and helps to theoretically understand the energy storage process of negative electrode materials under alkaline conditions.
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However, most of the research on the application of pure MnO2 in supercapacitors is mainly focused on positive electrode materials. In this work, we aim at studying the applicability and energy storage mechanism of MnO2 as a negative electrode material for supercapacitors, and compared three different crystalline MnO2 (δ-, β-, and α-MnO2). Additionally, the electrochemical performance of α-MnO2 was further improved by introducing oxygen vacancies generated at high temperature. Electrochemical studies show that M-300 (α-MnO2 heat-treated at 300 °C) electrode materials have a high specific capacitance of 736.3 F g−1 at 1 A g−1, and exhibit remarkable cycling stability. Impressively, hydroxide ion dependence experiments and research of the electron transfer mechanism during charge and discharge indicate that the charge storage process of MnO2 as a negative electrode is realized by the participation of OH− and the mutual conversion of Mn(ii), Mn(iii) and Mn(iv), absolutely different from the MnO2 positive electrode. We also theoretically quantified the contribution of the diffusion-controlled process and surface capacitance effects to investigate its energy storage mechanism. The assembled M-300//H-NiCo2O4 asymmetric supercapacitor exhibits excellent energy density (34.9 W h kg−1) and cycling stability (80.6% after 10 000 cycles). 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Impressively, hydroxide ion dependence experiments and research of the electron transfer mechanism during charge and discharge indicate that the charge storage process of MnO2 as a negative electrode is realized by the participation of OH− and the mutual conversion of Mn(ii), Mn(iii) and Mn(iv), absolutely different from the MnO2 positive electrode. We also theoretically quantified the contribution of the diffusion-controlled process and surface capacitance effects to investigate its energy storage mechanism. The assembled M-300//H-NiCo2O4 asymmetric supercapacitor exhibits excellent energy density (34.9 W h kg−1) and cycling stability (80.6% after 10 000 cycles). 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Impressively, hydroxide ion dependence experiments and research of the electron transfer mechanism during charge and discharge indicate that the charge storage process of MnO2 as a negative electrode is realized by the participation of OH− and the mutual conversion of Mn(ii), Mn(iii) and Mn(iv), absolutely different from the MnO2 positive electrode. We also theoretically quantified the contribution of the diffusion-controlled process and surface capacitance effects to investigate its energy storage mechanism. The assembled M-300//H-NiCo2O4 asymmetric supercapacitor exhibits excellent energy density (34.9 W h kg−1) and cycling stability (80.6% after 10 000 cycles). 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subjects Capacitance
Charge transfer
Cycles
Electrochemical analysis
Electrochemistry
Electrode materials
Electrodes
Electron transfer
Energy storage
Fabrication
Flux density
Heat treatment
High temperature
Ions
Lithium
Manganese
Manganese dioxide
Oxygen
Stability
Supercapacitors
Vacancies
title Hydroxide ion dependent α-MnO2 enhanced via oxygen vacancies as the negative electrode for high-performance supercapacitors
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