学术文献库

Low power photon upconversion (UC) based on sensitized triplet-triplet annihilation (sTTA) is considered as the most promising upwards wavelength-shifting technique to enhance the light harvesting capability of solar devices by recovering the low-energy tail of the solar spectrum. Semiconductor nanocrystals (NCs) with conjugated organic ligands have been proposed as broadband sensitizers for extending the light-harvesting capability of sTTA-UC molecular absorbers. Key to their functioning is efficient energy transfer (ET) from the NC to the triplet state of the ligands that sensitizes the triplet state of free emitters, whose annihilation generates the upconverted emission. To date, the triplet sensitization efficiency in such systems is limited by parasitic processes, such as charge transfer (typically of the photohole) to the organic ligand due to the disadvantageous band alignment of typical NCs and organic moieties. Available strategies only partially mitigate such losses and intrinsically limit the ET yield. Here we demonstrate a new exciton-manipulation approach that enables loss-free ET without detrimental side-effects. Specifically, we use CdSe NCs doped with gold atoms featuring a hole-accepting state in the NC bandgap at a higher energy than the HOMO level of the ligand 9-anthracene acid. Upon photoexcitation, the NC photoholes are routed to the Au-state faster than their transfer to the ligand, producing a long-lived bound exciton in perfect resonance with its triplet state. This hinders hole-transfer losses and results in ~100% efficient ET, over 50-fold higher than in standard NCs. By combining our hybrid sensitizers with an annihilator moiety, we achieved an sTTA-UC efficiency of ~12% (~24% in the normalized definition), which is the highest value for hybrid upconverters based on sTTA reported to date and approaches optimized organic systems.