Suppr超能文献

界面处 Ti-H 物种的形成对基于 TiO 的染料敏化器件的效率有致命影响。

The Formation of Ti-H Species at Interface Is Lethal to the Efficiency of TiO-Based Dye-Sensitized Devices.

机构信息

Key Laboratory of Photochemistry and State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences , Beijing, P. R. China 100190.

School of Chemistry and Chemical Engineering, Jiangsu University , No. 301, Xuefu Road, Zhenjiang, P. R. China 212013.

出版信息

J Am Chem Soc. 2017 Feb 8;139(5):2083-2089. doi: 10.1021/jacs.6b12324. Epub 2017 Jan 24.

Abstract

TiO-based dye-sensitization cycle is one of the basic strategies for the development of solar energy applications. Although the power conversion efficiency (PCE) of dye-sensitized devices has been improved through constant attempts, the intrinsically fatal factor that leads to the complete failure of the PCE of TiO-mediated dye-sensitized devices has not yet been determined. Here, by using isotopically labeled MAS-H NMR, ATR-FTIR spectroscopy (separate H/D and Ti/Ti experiments), and ESR, we revealed that the accumulative formation of Ti-H species on the TiO surface is the intrinsic cause of the PCE failure of TiO-based dye-sensitization devices. Such a Ti-H species is generated from the reduction of hydrogen ions (mostly released from dye carboxyl groups or organic electrolyte) accompanied by electron injection on the surface of TiO, which deteriorates the PCE mainly by reducing the electrical conductivity of the TiO (by a maximum of ∼80%) and the hydrophilic nature of the TiO surface (contact angle increased).

摘要

基于 TiO 的染料敏化循环是开发太阳能应用的基本策略之一。尽管通过不断尝试已经提高了染料敏化器件的功率转换效率(PCE),但导致 TiO 介导的染料敏化器件 PCE 完全失效的内在致命因素尚未确定。在这里,我们通过使用同位素标记的 MAS-H NMR、ATR-FTIR 光谱(单独的 H/D 和 Ti/Ti 实验)和 ESR,揭示了 TiO 表面上 Ti-H 物种的累积形成是 TiO 基染料敏化器件 PCE 失效的内在原因。这种 Ti-H 物种是由 TiO 表面上电子注入伴随的氢离子(主要来自染料羧酸基团或有机电解质)还原产生的,主要通过降低 TiO 的电导率(最大降低约 80%)和 TiO 表面的亲水性(接触角增大)来降低 PCE。

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