Maffeis Valentin, Dogan Hakan, Cassette Elsa, Jousselme Bruno, Gustavsson Thomas
LIDYL, CEA, CNRS, Université Paris-Saclay, F-91191 Gif-sur-Yvette, France.
LICSEN, NIMBE, CEA, CNRS, Université Paris-Saclay, CEA Saclay 91191 Gif-sur-Yvette Cedex, France.
J Phys Chem Lett. 2019 Sep 5;10(17):5076-5081. doi: 10.1021/acs.jpclett.9b01947. Epub 2019 Aug 20.
There is a growing consensus that the charge separation taking place in dye-sensitized solar cells is a multiscale process occurring on a times scale from a few to hundreds of picoseconds. We studied the excited-state dynamics of the robust and efficient push-pull dye in solution, on mesoporous films and in complete photovoltaics cells by femtosecond fluorescence upconversion and transient absorption. In a polar environment and cells, the dynamics at early times are dominated by an intramolecular electronic relaxation, while electron injection is predominant on thin films only. In cells, the electron injection process becomes visible at a later stage, from tens to hundreds of picoseconds. Our study shows that it is crucial to record and analyze full time-resolved fluorescence spectra in order to obtain wavelength-independent dynamics and get a correct description of the nature and the population of the excited state.
越来越多的人达成共识,即染料敏化太阳能电池中发生的电荷分离是一个多尺度过程,发生时间尺度从几皮秒到数百皮秒不等。我们通过飞秒荧光上转换和瞬态吸收研究了这种坚固且高效的推拉型染料在溶液中、介孔薄膜上以及完整光伏电池中的激发态动力学。在极性环境和电池中,早期的动力学主要由分子内电子弛豫主导,而电子注入仅在薄膜上占主导。在电池中,电子注入过程在后期(从几十皮秒到数百皮秒)变得明显。我们的研究表明,记录和分析全时间分辨荧光光谱对于获得与波长无关的动力学以及正确描述激发态的性质和数量至关重要。