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敏化卟啉体系用于具有 TOF-SIMS 分析的高性能太阳能电池。

Cosensitized Porphyrin System for High-Performance Solar Cells with TOF-SIMS Analysis.

机构信息

Key Laboratory for Advanced Materials and Institute of Fine Chemicals, Centre for Computational Chemistry, Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology , Shanghai 200237, China.

Key Laboratory of Organic Solids, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.

出版信息

ACS Appl Mater Interfaces. 2017 May 17;9(19):16081-16090. doi: 10.1021/acsami.7b00281. Epub 2017 May 2.

Abstract

To date, development of organic sensitizers has been predominately focused on light harvesting, highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels, and the electron transferring process. In contrast, their adsorption mode as well as the dynamic loading behavior onto nanoporous TiO is rarely considered. Herein, we have employed the time-of-flight secondary ion mass spectrometry (TOF-SIMS) to gain insight into the competitive dye adsorption mode and kinetics in the cosensitized porphyrin system. Using novel porphyrin dye FW-1 and D-A-π-A featured dye WS-5, the different bond-breaking mode in TOF-SIMS and dynamic dye-loading amount during the coadsorption process are well-compared with two different anchoring groups, such as benzoic acid and cyanoacrylic acid. With the bombardment mode in TOF-SIMS spectra, we have speculated that the cyano group grafts onto nanoporous TiO as tridentate binding for the common anchoring unit of cyanoacrylic acid and confirmed it through extensive first-principles density functional theory calculation by anchoring either the carboxyl or cyano group, which shows that the cyano group can efficiently participate in the adsorption of the WS-5 molecule onto the TiO nanocrystal. The grafting reinforcement interaction between the cyano group and TiO in WS-5 can well-explain the rapid adsorption characteristics. A strong coordinate bond between the lone pair of electrons on the nitrogen or oxygen atom and the Lewis acid sites of TiO can increase electron injection efficiencies with respect to those from the bond between the benzoic acid group and the Brønsted acid sites of the TiO surface. Upon optimization of the coadsorption process with dye WS-5, the photoelectric conversion efficiency based on porphyrin dye FW-1 is increased from 6.14 to 9.72%. The study on the adsorption dynamics of organic sensitizers with TOF-SIMS analysis might provide a new venue for improvement of cosensitized solar cells.

摘要

迄今为止,有机敏化剂的发展主要集中在光捕获、最高占据分子轨道和最低未占据分子轨道能级以及电子转移过程上。相比之下,很少考虑它们的吸附模式以及在纳米多孔 TiO 上的动态负载行为。在此,我们采用飞行时间二次离子质谱(TOF-SIMS)来深入了解共敏化卟啉体系中的竞争染料吸附模式和动力学。使用新型卟啉染料 FW-1 和 D-A-π-A 型染料 WS-5,我们比较了两种不同的键断模式和在共吸附过程中动态染料负载量,这两种不同的键断模式涉及两种不同的锚定基团,如苯甲酸和氰基丙烯酸。通过 TOF-SIMS 光谱中的轰击模式,我们推测氰基基团以三齿配位形式接枝到纳米多孔 TiO 上,这是氰基丙烯酸的常见锚定单元,并通过广泛的第一性原理密度泛函理论计算来证实这一点,即通过锚定羧基或氰基基团,氰基基团可以有效地参与 WS-5 分子在 TiO 纳米晶上的吸附。WS-5 中氰基基团与 TiO 之间的接枝增强相互作用可以很好地解释快速吸附特性。氮或氧原子上的孤对电子与 TiO 的路易斯酸位之间的强配位键可以提高电子注入效率,而不是通过苯甲酸基团与 TiO 表面的布朗斯台德酸位之间的键来提高电子注入效率。通过优化 WS-5 的共吸附过程,基于卟啉染料 FW-1 的光电转换效率从 6.14%提高到 9.72%。通过 TOF-SIMS 分析研究有机敏化剂的吸附动力学可能为改进共敏化太阳能电池提供新途径。

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