Influence of Water on the Electronic: and Molecular Surface Structures of Ru-Dyes at Nanostructured TiO2

被引:28
作者
Hahlin, Maria [1 ]
Johansson, Erik M. J. [2 ]
Scholin, Rebecka [1 ]
Siegbabn, Hans [1 ]
Rensmo, Hakan [1 ]
机构
[1] Uppsala Univ, Dept Phys & Astron, S-75120 Uppsala, Sweden
[2] Uppsala Univ, Dept Phys & Analyt Chem, S-75105 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
SENSITIZED SOLAR-CELLS; INTERFACIAL PROPERTIES; PHOTOELECTRON-SPECTROSCOPY; CHARGE-TRANSFER; ADSORPTION; EFFICIENCY; CONVERSION; COMPLEXES; LIGHT; PHOTOSENSITIZERS;
D O I
10.1021/jp1076609
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The influence of water on the surface electronic and molecular properties of three Ru-dyes adsorbed at nanostructured TiO2 was investigated using photoelectron spectroscopy (PES). The dyes investigated were the Ru(dcbpy)(2)(NCS)(2) in its acid (N3) and in its 2-fold deprotonated form (N719) as well as a similar dye (Z-907) containing the hydrophobic ligand 4,4'-dinonyl-2,2'-bipyridine. Trends in surface structures depending on water exposure were followed for the three dyes. The results showed that the hydrophobic chains of the Z-907 dye effectively inhibit surface reorganization while large changes in surface electronic and molecular structure were observed for the N3 and N719 molecular layers. Specifically, large effects involving the thiocyanate ligands were detected, and the S2p and N Is core level spectra indicate that the changes involve mixing of only two dominating surface configurations. Moreover, the PES results also showed water-induced changes in the energy level matching between the dye and the TiO2, and water induced desorption of the TBA(+) counterion. Basic photoelectrochemical trends depending on water exposure to dye-sensitized solar cell systems were also verified.
引用
收藏
页码:11996 / 12004
页数:9
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