Xie Xiaoyin, Liu Zhi-Hai, Bai Fu-Quan, Zhang Hong-Xing
International Joint Research Laboratory of Nano-Micro Architecture Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun, China.
Department of Chemical Technology, Jilin Institute of Chemical Technology, Jilin, China.
Front Chem. 2019 Jan 29;6:676. doi: 10.3389/fchem.2018.00676. eCollection 2018.
Dye-sensitized solar cells (DSSCs) have been widely investigated; however, the development of promising dye sensitizers is still appealing. In this work, we perform a detailed theoretical search for high-efficiency D-π-A organic dyes using density functional theory and time-dependent density functional theory calculations. Specifically, we perform geometric optimization, and electronic structure and absorption spectra calculations for isolated dyes for two thieno[3,2-b]benzothiophene π-spacer-based D-π-A organic dyes SGT129 and SGT130, which show significant efficiency difference, before and after binding to a TiO semiconductor. The calculation results reveal that the coplanar configuration between the electron donor and the π-spacer can enhance electronic communication efficiently, thus facilitating intra-molecular charge transfer from the electron donor to the acceptor groups in SGT130. The absorption spectrum of SGT130 broadens and is red-shifted owing to the decreased bandgap. The higher light-harvesting efficiency, favorable intra-molecular charge transfer, larger shift of the conduction band edge in the TiO semiconductor, and slower charge recombination between the injected electrons in the TiO conduction band and the electrolyte explain the superior efficiency of SGT130 over that of SGT129. Using SGT130 as the reference dye, we further design four novel dyes - by modifying the π-spacer with electron-rich and electron-withdrawing moieties. Judging from the theoretical parameters influencing the short-circuit current and open-circuit voltage, we found that all dyes would perform better than SGT130 in terms of the favorable interfacial charge transfer (ICT) and light-harvesting efficiency, as well as the larger shift of the TiO conduction band edge. Our theoretical research is expected to provide valuable insights into the molecular modification of TBT-based D-π-A organic dyes for DSSC applications.
染料敏化太阳能电池(DSSC)已得到广泛研究;然而,开发有前景的染料敏化剂仍然具有吸引力。在这项工作中,我们使用密度泛函理论和含时密度泛函理论计算对高效D-π-A有机染料进行了详细的理论搜索。具体而言,我们对两种基于噻吩并[3,2-b]苯并噻吩π-间隔基的D-π-A有机染料SGT129和SGT130进行了几何优化、电子结构和吸收光谱计算,这两种染料在与TiO半导体结合前后表现出显著的效率差异。计算结果表明,电子供体与π-间隔基之间的共面构型可以有效地增强电子通信,从而促进SGT130中分子内电荷从电子供体向受体基团的转移。由于带隙减小,SGT130的吸收光谱变宽并发生红移。更高的光捕获效率、有利的分子内电荷转移、TiO半导体中导带边缘的更大位移以及TiO导带中注入电子与电解质之间较慢的电荷复合,解释了SGT130比SGT129具有更高的效率。以SGT130作为参考染料,我们进一步设计了四种新型染料——通过用富电子和吸电子基团修饰π-间隔基。从影响短路电流和开路电压的理论参数来看,我们发现所有染料在有利的界面电荷转移(ICT)和光捕获效率以及TiO导带边缘的更大位移方面都将比SGT130表现更好。我们的理论研究有望为用于DSSC应用的基于TBT的D-π-A有机染料的分子修饰提供有价值的见解。