Suppr超能文献

亚硝酸盐增强的单根聚苯胺纳米管的电荷转移

Nitrite-Enhanced Charge Transfer to and from Single Polyaniline Nanotubes.

作者信息

Liu Jianyun, Li Xiuting, Batchelor-McAuley Christopher, Zhu Guodong, Compton Richard G

机构信息

State Environmental Protection Engineering Center for Pollution Treatment and Control in the Textile Industry, College of Environmental Science and Engineering, Donghua University, Shanghai, 201620, China.

Department of Chemistry, Physical and Theoretical Chemistry Laboratory, University of Oxford, Oxford, OX1 3QZ, UK.

出版信息

Chemistry. 2017 Dec 14;23(70):17823-17828. doi: 10.1002/chem.201704055. Epub 2017 Nov 16.

Abstract

As Liu et al. reported previously (Appl. Mater. Today 2017, 7, 239-245), the charge transfer to partially oxidized polyaniline (PANI) nanotubes in electrochemical reactions is heavily limited due to the non-conductivity of the reduction/oxidation products. In this paper, the doping level of individual PANI nanotubes was substantially enhanced using nitrite as an electron acceptor in sulfuric acid aqueous solution as recorded by the nano-impact method. The charge transferred to one single tube during reduction process is close to the theoretical value of 170±112 pC per tube (assuming 2-electron reduction for the PANI tubes studied), while the charge during PANI oxidation is dramatically decreased. Reaction processes are proposed based on the oxidative properties of nitrite in acid solution. UV-visible spectroscopy analysis further confirms an oxidation-reduction reaction between PANI and nitrite. In contrast the electrochemical reaction of ensembles (21 μg cm ) of PANI tubes on glassy carbon electrodes simply show limited electrocatalytic activity.

摘要

正如刘等人之前所报道的(《应用材料今日》,2017年,第7期,239 - 245页),由于还原/氧化产物的非导电性,在电化学反应中电荷向部分氧化的聚苯胺(PANI)纳米管的转移受到严重限制。在本文中,通过纳米冲击法记录,在硫酸水溶液中使用亚硝酸盐作为电子受体,单个PANI纳米管的掺杂水平得到了显著提高。在还原过程中转移到单个管子的电荷接近每管170±112 pC的理论值(假设所研究的PANI管为2电子还原),而在PANI氧化过程中的电荷则显著降低。基于亚硝酸盐在酸性溶液中的氧化性质提出了反应过程。紫外 - 可见光谱分析进一步证实了PANI与亚硝酸盐之间的氧化还原反应。相比之下,玻碳电极上PANI管集合体(21 μg cm)的电化学反应仅显示出有限的电催化活性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验