4.7 Article

In-situ hydrothermal synthesis of MnO2/NiO@Ni hetero structure electrode for hydrogen evolution reaction and high energy asymmetric supercapacitor applications

期刊

JOURNAL OF ENERGY STORAGE
卷 6, 期 -, 页码 22-31

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.est.2016.02.007

关键词

Multi-metal oxide; Binder free electrode; Hydrogen evalution reaction; Thermaly reduced graphene oxide; Asymmetric device; Energy density

资金

  1. Department of Science and Technology, New Delhi, India from DST-INSPIRE Faculty Scheme-INSPIRE Programme [IFA12CH-47]
  2. Council of Scientific and Industrial Research, New Delhi, India [ESC0112/RP-II]
  3. R&D Convergence Program of MSIP (Ministry of Science, ICT and Future Planning) of Republic of Korea [CAP-13-2-ETRI]
  4. KIST Institutional Program

向作者/读者索取更多资源

In-situ deposition of MnO2/NiO hetero structure on Ni-foam has been carried out through simple one-step hydrothermal reaction. The in-situ deposited multi-metal oxide shows extraordinary electrocatalytic activity in hydrogen evolution reaction with a small Tafel slope of 38 mV per decade and very low onset potential of 0.17 V. An electrolyser has been fabricated with MnO2/NiO deposited Ni-foam which effectively achieves a current density of similar to 24 mA cm(-2) at an applied voltage of similar to 1.57 V. Furthermore, the metal oxide deposited on Ni-foam is directly used as the supercapacitor electrode which shows good rate capability as positive electrode materials. An asymmetric capacitor (ASC) has been assembled by using the MnO2/NiO deposited Ni-foam as positive electrode and thermally reduced graphene oxide as negative electrode. The assembled ASC has a large specific capacitance of 218 F g(-1) at a current density of 3 A g(-1) and can deliver high energy and power density of 59.5 Wh kg(-1) and 25,350 W kg(-1), respectively. The ASC shows very good electrochemical stability throughout 10,000 charge-discharge cycles along with the capability to work in the high frequency range. (C) 2016 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据