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通过水溶液中的阴离子交换碲化策略形成用于电催化应用的半金属碲化钴纳米管膜。

Formation of Semimetallic Cobalt Telluride Nanotube Film via Anion Exchange Tellurization Strategy in Aqueous Solution for Electrocatalytic Applications.

机构信息

Department of Chemistry, Hanyang University , Seongdong-gu, Haengdang-dong 17, Seoul 133-791, Republic of Korea.

Sungshin Women's University, School of Biological Science and Chemistry , 55 Dobong-ro 76 ga-gil, Gangbuk-gu, Seoul 142-732, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2015 Nov 25;7(46):25914-22. doi: 10.1021/acsami.5b08501. Epub 2015 Nov 11.

Abstract

Metal telluride nanostructures have demonstrated several potential applications particularly in harvesting and storing green energy. Metal tellurides are synthesized by tellurization process performed basically at high temperature in reducing gas atmosphere, which makes the process expensive and complicated. The development of a facile and economical process for desirable metal telluride nanostructures without complicated manipulation is still a challenge. In an effort to develop an alternative strategy of tellurization, herein we report a thin film formation of self-standing cobalt telluride nanotubes on various conducting and nonconducting substrates using a simple binder-free synthetic strategy based on anion exchange transformation from a thin film of cobalt hydroxycarbonate nanostructures in aqueous solution at room temperature. The nanostructured films before and after ion exchange transformation reaction are characterized using field emission scanning electron microscope, energy dispersive X-ray analyzer, X-ray photoelectron spectroscopy, thin film X-ray diffraction technique, high resolution transmission electron microscope, and selected area electron diffraction analysis technique. After the ion exchange transformation of nanostructures, the film shows conversion from insulator to highly electrical conductive semimetallic characteristic. When used as a counter electrode in I3(-)/I(-) redox electrolyte based dye-sensitized solar cells, the telluride film exhibits an electrocatalytic reduction activity for I3(-) with a demonstration of solar-light to electrical power conversion efficiency of 8.10%, which is highly competitive to the efficiency of 8.20% exhibited by a benchmarked Pt-film counter electrode. On the other hand, the telluride film electrode also demonstrates electrocatalytic activity for oxygen evolution reaction from oxidation of water.

摘要

金属碲化物纳米结构具有多种潜在应用,特别是在绿色能源的收集和存储方面。金属碲化物是通过在还原气体气氛中基本在高温下进行的碲化过程合成的,这使得该过程昂贵且复杂。开发一种简单且经济的方法来制备所需的金属碲化物纳米结构,而无需复杂的操作,仍然是一个挑战。为了开发一种替代的碲化策略,本文报道了一种在各种导电和非导电衬底上自支撑的钴碲化物纳米管的薄膜形成方法,该方法使用基于阴离子交换的简单无粘合剂合成策略,在室温下从水溶液中的钴羟基碳酸盐纳米结构薄膜中进行。使用场发射扫描电子显微镜、能谱分析仪、X 射线光电子能谱、薄膜 X 射线衍射技术、高分辨率透射电子显微镜和选区电子衍射分析技术对离子交换前后的纳米结构薄膜进行了表征。在离子交换反应后,薄膜的特征从绝缘体转变为高度电导率的半金属。当用作基于 I3(-)/I(-)氧化还原电解质的染料敏化太阳能电池的对电极时,碲化物薄膜表现出对 I3(-)的电催化还原活性,其展示的太阳能到电能的转换效率为 8.10%,与基准 Pt 薄膜对电极的 8.20%的效率相当。另一方面,碲化物薄膜电极还表现出对水氧化反应的析氧反应的电催化活性。

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