• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

双面阳极氧化钛纳米管阵列:一种不对称的生长过程。

Double-sided anodic titania nanotube arrays: a lopsided growth process.

机构信息

School of Mechanical and Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Singapore.

出版信息

Langmuir. 2010 Dec 7;26(23):18424-9. doi: 10.1021/la103390s. Epub 2010 Nov 4.

DOI:10.1021/la103390s
PMID:21049918
Abstract

In the past decade, the pore diameter of anodic titania nanotubes was reported to be influenced by a number of factors in organic electrolyte, for example, applied potential, working distance, water content, and temperature. All these were closely related to potential drop in the organic electrolyte. In this work, the essential role of electric field originating from the potential drop was directly revealed for the first time using a simple two-electrode anodizing method. Anodic titania nanotube arrays were grown simultaneously at both sides of a titanium foil, with tube length being longer at the front side than that at the back side. This lopsided growth was attributed to the higher ionic flux induced by electric field at the front side. Accordingly, the nanotube length was further tailored to be comparable at both sides by modulating the electric field. These results are promising to be used in parallel configuration dye-sensitized solar cells, water splitting, and gas sensors, as a result of high surface area produced by the double-sided architecture.

摘要

在过去的十年中,研究人员发现阳极氧化钛纳米管的孔径受有机电解液中多种因素的影响,例如施加的电势、工作距离、含水量和温度。所有这些都与有机电解液中的电势降密切相关。在这项工作中,首次使用简单的两电极阳极氧化法直接揭示了源自电势降的电场的重要作用。钛箔的两侧同时生长阳极氧化钛纳米管阵列,前侧的管长比后侧长。这种不对称生长归因于前侧电场引起的更高离子通量。因此,通过调节电场,将纳米管长度进一步调整为两侧可比。这些结果有望用于平行配置的染料敏化太阳能电池、水分解和气体传感器,因为双面结构产生了高表面积。

相似文献

1
Double-sided anodic titania nanotube arrays: a lopsided growth process.双面阳极氧化钛纳米管阵列:一种不对称的生长过程。
Langmuir. 2010 Dec 7;26(23):18424-9. doi: 10.1021/la103390s. Epub 2010 Nov 4.
2
Hierarchical titania nanotubes with self-branched crystalline nanorods.具有自分支晶状纳米棒的分级二氧化钛纳米管。
ACS Appl Mater Interfaces. 2010 Jun;2(6):1581-7. doi: 10.1021/am100299e.
3
Vertically oriented Ti-Pd mixed oxynitride nanotube arrays for enhanced photoelectrochemical water splitting.垂直取向的 Ti-Pd 混合氮氧化物纳米管阵列用于增强光电化学水分解。
ACS Nano. 2011 Jun 28;5(6):5056-66. doi: 10.1021/nn201136t. Epub 2011 May 13.
4
Selective removal of the outer shells of anodic TiO2 nanotubes.选择性去除阳极 TiO2 纳米管的外壳。
Small. 2013 Jan 14;9(1):37-44. doi: 10.1002/smll.201201874. Epub 2012 Oct 9.
5
Application of highly ordered TiO2 nanotube arrays in flexible dye-sensitized solar cells.高度有序的TiO₂纳米管阵列在柔性染料敏化太阳能电池中的应用
ACS Nano. 2008 Jun;2(6):1113-6. doi: 10.1021/nn800174y.
6
Anodic growth of highly ordered TiO2 nanotube arrays to 134 microm in length.高度有序的TiO₂纳米管阵列的阳极生长至长度为134微米。
J Phys Chem B. 2006 Aug 24;110(33):16179-84. doi: 10.1021/jp064020k.
7
Anodic titania nanotubes grown on titanium tubular electrodes.
Langmuir. 2014 Mar 18;30(10):2835-41. doi: 10.1021/la500050q. Epub 2014 Mar 6.
8
Fabrication of highly ordered TiO2 nanorod/nanotube adjacent arrays for photoelectrochemical applications.用于光电化学应用的高度有序 TiO2 纳米棒/纳米管相邻阵列的制造。
Langmuir. 2010 Jul 6;26(13):11226-32. doi: 10.1021/la1005314.
9
Enhanced photoassisted water electrolysis using vertically oriented anodically fabricated Ti-Nb-Zr-O mixed oxide nanotube arrays.采用阳极制备的垂直取向 Ti-Nb-Zr-O 混合氧化物纳米管阵列增强光电辅助水分解。
ACS Nano. 2010 Oct 26;4(10):5819-26. doi: 10.1021/nn101678n.
10
Transition from anodic titania nanotubes to nanowires: arising from nanotube growth to application in dye-sensitized solar cells.从阳极氧化钛纳米管到纳米线的转变:源于纳米管生长及其在染料敏化太阳能电池中的应用。
Chemphyschem. 2011 Dec 23;12(18):3634-41. doi: 10.1002/cphc.201100450. Epub 2011 Nov 7.