Fort Madeleine J, Click Sophia M, Robinson Evan H, He Felix M C, Bernhardt Paul V, Rosenthal Sandra J, Macdonald Janet E
Department of Chemistry, Vanderbilt Institute of Nanoscale Science and Engineering, Vanderbilt University, Nashville, TN 37235, USA.
School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Queensland, 4072, Australia.
Angew Chem Int Ed Engl. 2022 Jul 4;61(27):e202202322. doi: 10.1002/anie.202202322. Epub 2022 May 12.
Light-induced charge separation is at the very heart of many solar harvesting technologies. The reduction of energetic barriers to charge separation and transfer increases the rate of separation and the overall efficiency of these technologies. Here we report that the internal reorganization energy of the redox acceptor, the movement of the atoms with changing charge, has a profound effect on the charge transfer rates from donor quantum dots. We experimentally studied and modelled with Marcus Theory charge transfer to cobalt complexes that have similar redox potentials covering 350 mV, but vastly different reorganization energies spanning 2 eV. While the driving force does influence the electron transfer rates, the reorganization energies had a far more profound effect, increasing charge transfer rates by several orders of magnitude. Our studies suggest that careful design of redox mediators to minimize reorganization energy is an untapped route to drastically increase the efficiency of quantum dot applications that feature charge transfer.
光诱导电荷分离是许多太阳能收集技术的核心所在。降低电荷分离和转移的能量势垒可提高这些技术的分离速率和整体效率。在此,我们报告氧化还原受体的内部重组能,即随着电荷变化的原子运动,对来自供体量子点的电荷转移速率有深远影响。我们通过实验研究并运用马库斯理论对钴配合物的电荷转移进行建模,这些钴配合物具有相似的氧化还原电位,范围为350毫伏,但重组能差异极大,跨度达2电子伏特。虽然驱动力确实会影响电子转移速率,但重组能的影响更为深远,可将电荷转移速率提高几个数量级。我们的研究表明,精心设计氧化还原介质以最小化重组能是大幅提高以电荷转移为特征的量子点应用效率的一条尚未开发的途径。