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- W4229364549 abstract "Due to the large distance or weak electronic conjugation between adjacent Bi-I octahedrons, the charge transport in the low-dimensional bismuth-based hybrid perovskites is impeded and thus hinders their future developments. In this work, A-site cation engineering by monoamine BZA (benzylamine) and diamine 3-AMP (3-(aminomethyl)pyridine) has been demonstrated as an efficient strategy to regulate the corresponding activation energy of ionic migration and carrier transport capacity. Given the higher polarity of 3-AMP than BZA, producing a more efficient dielectric screening effect, it gives rise to obtaining the small exciton binding energy (50 meV) and low defect states (3.53×109 cm-3 ). The reduced distance of adjacent Bi-I octahedrons by the bilateral anchoring of the 3-AMP2+ diamine cation enhances both electronic conjugation and charge transport performance. Therefore, the photodetector for (3-AMP)BiI5 SC shows a 243-fold increase in on/off ratio compared with the (BZA)3 BiI6 SC." @default.
- W4229364549 created "2022-05-10" @default.
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- W4229364549 date "2022-05-23" @default.
- W4229364549 modified "2023-10-01" @default.
- W4229364549 title "A‐Site Diamine Cation Anchoring Enables Efficient Charge Transfer and Suppressed Ion Migration in Bi‐Based Hybrid Perovskite Single Crystals" @default.
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- W4229364549 doi "https://doi.org/10.1002/anie.202204663" @default.
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