橡胶
钙钛矿(结构)
材料科学
光子上转换
光谱学
三重态
兴奋剂
光电子学
化学物理
光化学
化学
分子
结晶学
物理
有机化学
量子力学
作者
Colette M. Sullivan,Alexander S. Bieber,Hayley K. Drozdick,Gregory Moller,Jason E. Kuszynski,Zachary A. VanOrman,Sarah Wieghold,Geoffrey F. Strouse,Lea Nienhaus
标识
DOI:10.1002/adom.202201921
摘要
Abstract Triplet–triplet annihilation‐based photon upconversion (TTA‐UC) can efficiently generate higher energy photons at low relative fluences. Bulk metal halide perovskites have offered promise in efficiently sensitizing molecular triplet states in the solid state, necessary for the integration of TTA‐UC into device‐based applications. Recent work focused on TTA‐UC from a rubrene triplet annihilator sensitized by perovskite thin films has established relatively efficient charge extraction from the perovskite, forming the triplet exciton in rubrene. Yet, the specifics underpinning charge transfer at the perovskite/rubrene interface are not fully elucidated. To improve device performance and study the properties governing charge transfer at the interface, various organic solvents are explored to treat the perovskite surface. Scanning tunneling microscopy and spectroscopy show a difference in the electronic band structure, where both n‐ and p‐type terminated perovskite surfaces are observed depending on the solvent used. Supported by optical spectroscopy, the impact of the perovskite electronic structure is monitored, indicating that n‐type perovskite sensitizers feature higher TTA‐UC efficiencies due to favorable band bending resulting in efficient hole‐mediated triplet formation. Overall, the tuning of the electronic structure of the perovskite sensitizer through solvent treatment is shown to be a key force in tuning the mechanism of efficient triplet generation.
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