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用于电催化氧还原的氧化锰纳米结构的选择性合成。

Selective synthesis of manganese oxide nanostructures for electrocatalytic oxygen reduction.

机构信息

Institute of New Energy Materials Chemistry and Key Laboratory of Energy Materials Chemistry (Tianjin), Chemistry College, Nankai University, Tianjin, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2009 Feb;1(2):460-6. doi: 10.1021/am800131v.

Abstract

This work presents two points with respect to manganese oxide (MnO(x)) nanomaterials: their controllable synthesis with desired phases and shapes together with their applications as catalysts for oxygen reduction and Al/air batteries. Solid MnO(x) with crystalline phases of MnOOH, Mn(2)O(3), and MnO(2) as well as shapes of the sphere, wire, rod, and particle were prepared through a simple one-pot hydrothermal route. Selective preparation was achieved by adjusting the surfactant concentration that controls simultaneously the growth thermodynamic and dynamic parameters of MnO(x) nanocrystals. Electrochemical investigations show that the obtained Mn(2)O(3) nanowires, which possess a large aspect ratio and preferentially exposed (222) crystal surfaces, exhibit remarkable catalytic activity (comparable to Pt/C counterparts) toward the electroreduction of oxygen in alkaline media. The tailored MnO(x) nanostructures may find prospective applications as low-cost catalysts for alkaline fuel cells and metal/air batteries.

摘要

本文主要讨论了氧化锰 (MnO(x)) 纳米材料的两个方面:其可控合成具有所需相和形状,以及作为氧还原和 Al/空气电池催化剂的应用。通过简单的一步水热法制备了具有 MnOOH、Mn(2)O(3)和 MnO(2)晶相以及球形、线状、棒状和颗粒状的固态 MnO(x)。通过调整表面活性剂浓度,可以同时控制 MnO(x)纳米晶体的生长热力学和动力学参数,从而实现选择性制备。电化学研究表明,所获得的具有大纵横比且优先暴露 (222) 晶面的 Mn(2)O(3)纳米线在碱性介质中对氧的还原具有显著的催化活性(可与 Pt/C 相媲美)。经过剪裁的 MnO(x) 纳米结构可用作低成本催化剂,应用于碱性燃料电池和金属/空气电池。

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