Instituto de Física , Benemérita Universidad Autónoma de Puebla , Apdo. Postal J-48 , Puebla , Puebla 72570 , Mexico.
Advanced Light Source , Lawrence Berkeley National Laboratory , 1 Cyclotron Road , Berkeley , California 94720 , United States.
ACS Appl Mater Interfaces. 2018 Sep 19;10(37):31374-31383. doi: 10.1021/acsami.8b10063. Epub 2018 Sep 7.
The incorporation of plasmonic nanostructures in active electrodes has become one of the most attractive ways to enhance the photoconversion efficiency (PCE) of dye-sensitized solar cells (DSSCs). Although an enhancement of PCE because of the incorporation of plasmonic nanostructures of different sizes, either bare or coated, has been demonstrated, the fundamental mechanisms associated to such enhancement are still unclear. Besides, the photocurrent enhancement of plasmonic DSSCs is frequently associated to the strong surface plasmon resonance (SPR) absorption of metal nanoparticles. In this work, through oxygen K-edge soft X-ray absorption and emission spectroscopies of plasmonic electrodes and electrodynamical characterization of the fabricated cells, we demonstrate a band gap narrowing and photocharging effect on the plasmonic electrodes that definitely contribute to the PCE enhancement in plasmonic DSSCs. The incorporation of bare metal nanoparticles in active metal-oxide semiconductor electrodes such as TiO in optimum concentration causes an upward shift of its valence band edge, reducing its effective band gap energy and enhancing the short-circuit current of DSSCs. On the other hand, small perturbation-based stepped light-induced transient measurements of photovoltage and photocurrent of the operating DSSCs revealed an upward shift of quasi-Fermi level of photoelectrodes because of the photocharging effect induced by the incorporated metal nanoparticles. The upward shift of the quasi-Fermi level causes an increase in open-circuit voltage ( V), nullifying the effect of band gap reduction. The short-circuit photocurrent enhancement was controlled by the band gap narrowing, screening the SPR contribution. The results presented in this work not only clarify the contribution of SPR absorption in plasmonic DSSCs, but also highlight the importance of considering the corrections in the effective base voltage because of the quasi-Fermi level band shift during the estimation of the transport and recombination parameters of an assembled DSSC.
将等离子体纳米结构纳入活性电极已成为提高染料敏化太阳能电池(DSSC)光电转换效率(PCE)的最吸引人的方法之一。尽管已经证明了由于不同尺寸的裸或涂覆的等离子体纳米结构的掺入而导致 PCE 的提高,但与这种提高相关的基本机制仍不清楚。此外,等离子体 DSSC 的光电流增强通常与金属纳米粒子的强表面等离子体共振(SPR)吸收有关。在这项工作中,通过等离子体电极的氧 K 边软 X 射线吸收和发射光谱以及所制造电池的电动力学特性,我们证明了等离子体电极的带隙变窄和光电荷效应,这绝对有助于提高等离子体 DSSC 的 PCE。在最佳浓度下将裸金属纳米粒子掺入活性金属氧化物半导体电极(如 TiO)中会导致其价带边缘上移,从而降低其有效带隙能量并提高 DSSC 的短路电流。另一方面,基于小扰动的阶跃光诱导瞬态光电压和光电流测量揭示了由于掺入的金属纳米粒子引起的光电荷效应,工作中的 DSSC 光电极的准费米能级向上移动。由于光电荷效应引起的准费米能级的上移导致开路电压(V)增加,抵消了带隙减小的影响。短路光电流增强受带隙变窄控制,屏蔽了 SPR 贡献。本工作中的结果不仅阐明了 SPR 吸收在等离子体 DSSC 中的贡献,而且强调了在估计组装 DSSC 的传输和复合参数时,由于准费米能级带的移位,考虑有效基电压校正的重要性。