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层状介孔 NiO/MnO@PANI 核壳微球,高效稳定的氧析出和还原反应双功能电催化剂。

Hierarchical Mesoporous NiO/MnO@PANI Core-Shell Microspheres, Highly Efficient and Stable Bifunctional Electrocatalysts for Oxygen Evolution and Reduction Reactions.

机构信息

Institute of Materials Science, University of Connecticut , Storrs, Connecticut 06269-3136, United States.

Key Lab of Advanced Ceramics and Machining Technology of Ministry of Education, Tianjin University , Tianjin 300072, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2017 Dec 13;9(49):42676-42687. doi: 10.1021/acsami.7b07383. Epub 2017 Dec 4.

Abstract

We report on the new facile synthesis of mesoporous NiO/MnO in one step by modifying inverse micelle templated UCT (University of Connecticut) methods. The catalyst shows excellent electrocatalytic activity and stability for both the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR) in alkaline media after further coating with polyaniline (PANI). For electrochemical performance, the optimized catalyst exhibits a potential gap, ΔE, of 0.75 V to achieve a current of 10 mA cm for the OER and -3 mA cm for the ORR in 0.1 M KOH solution. Extensive characterization methods were applied to investigate the structure-property of the catalyst for correlations with activity (e.g., XRD, BET, SEM, HRTEM, FIB-TEM, XPS, TGA, and Raman). The high electrocatalytic activity of the catalyst closely relates to the good electrical conductivity of PANI, accessible mesoporous structure, high surface area, as well as the synergistic effect of the specific core-shell structure. This work opens a new avenue for the rational design of core-shell structure catalysts for energy conversion and storage applications.

摘要

我们报告了一种新的简便合成介孔 NiO/MnO 的方法,该方法通过修饰反胶束模板 UCT(康涅狄格大学)方法一步合成。进一步用聚苯胺(PANI)涂覆后,催化剂在碱性介质中对析氧反应(OER)和氧还原反应(ORR)均表现出优异的电催化活性和稳定性。对于电化学性能,优化后的催化剂在 0.1 M KOH 溶液中表现出 0.75 V 的电位差,达到 10 mA cm 的 OER 电流和-3 mA cm 的 ORR 电流。广泛的表征方法被应用于研究催化剂的结构-性能与活性的相关性(例如,XRD、BET、SEM、HRTEM、FIB-TEM、XPS、TGA 和 Raman)。催化剂的高电催化活性与 PANI 的良好导电性、可及的介孔结构、高比表面积以及特定核壳结构的协同效应密切相关。这项工作为用于能量转换和存储应用的核壳结构催化剂的合理设计开辟了新途径。

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