Mehdipour Hamid, Kratzer Peter, Tafreshi Saeedeh S, Prezhdo Oleg
Faculty of Physics, University of Duisburg-Essen, 47057 Duisburg, Germany.
Department of Chemistry, Amirkabir University of Technology, 350 Hafez Avenue, Valiasr Square, 1591634311 Tehran, Iran.
J Phys Chem Lett. 2024 Aug 8;15(31):7878-7884. doi: 10.1021/acs.jpclett.4c01774. Epub 2024 Jul 26.
Organic light-absorbing materials with two-dimensional semiconductor layers as contact electrodes are promising for efficient and flexible low-cost solar cells. Considering anthracene as an absorber and a MoSSe Janus monolayer, we use non-adiabatic molecular dynamics to show that electron transfer from anthracene to MoSSe is faster on the Se side than the S side. The transfer from anthracene to MoS and MoSe monolayers takes intermediate times. As a rule, we find that a shorter adsorption distance produces a stronger donor-acceptor coupling. The smaller distance on the Se side is rationalized by the attractive force between the intrinsic dipole moment of the Janus structure and that of the molecule induced due to adsorption. Quantum coherence also affects the transfer time. The study provides detailed insights into adsorption of molecules on Janus structures and the resulting electronic and electron vibrational interactions. The results suggest that the dipole interaction plays an important role in the thermodynamic stability, alignment of electronic levels, and electron vibrational dynamics.
以二维半导体层作为接触电极的有机光吸收材料,对于高效、柔性且低成本的太阳能电池而言颇具前景。以蒽作为吸收体以及MoSSe Janus单层,我们运用非绝热分子动力学表明,从蒽到MoSSe的电子转移在Se侧比在S侧更快。从蒽到MoS和MoSe单层的转移耗时居中。通常,我们发现较短的吸附距离会产生更强的供体 - 受体耦合。Se侧较小的距离可通过Janus结构的固有偶极矩与因吸附而诱导的分子偶极矩之间的吸引力来解释。量子相干也会影响转移时间。该研究为分子在Janus结构上的吸附以及由此产生的电子和电子振动相互作用提供了详细的见解。结果表明,偶极相互作用在热力学稳定性、电子能级排列以及电子振动动力学中起着重要作用。