Molecular photon upconversion using organic-inorganic hybrid interfaces

    公开(公告)号:US10991517B2

    公开(公告)日:2021-04-27

    申请号:US15502448

    申请日:2015-08-25

    Abstract: Transmission of low energy light is one of the primary loss mechanisms of a single junction solar cell. Molecular photon upconversion via triplet-triplet annihilation (TTA-UC)—combining two or more low energy photons to generate a higher energy excited state—is an intriguing strategy to surpass this limit. The present disclosure is directed to self-assembled multilayers, e.g., bi- or trilayers, on metal oxide surfaces as a strategy to facilitate TTA-UC emission and demonstrate direct charge separation of the upconverted state. A three-fold enhancement in transient photocurrent is achieved at light intensities as low as two equivalent suns. The multilayer structure comprises a substrate comprising a metal oxide surface and a bulk region, and a self-assembled bilayer film, the bilayer film comprising: (a) an acceptor molecule covalently bonded to the metal oxide surface; (b) a linking metal ion bonded to the acceptor molecule; and (c) one or more sensitizer molecule(s) bonded to the linking coordinating metal ion.

    Modulating electron transfer dynamics at hybrid interfaces via self-assembled multilayers

    公开(公告)号:US10916381B2

    公开(公告)日:2021-02-09

    申请号:US15325788

    申请日:2015-07-14

    Abstract: Forward and back electron transfer at molecule oxide interfaces are pivotal events in dye-sensitized solar cells, dye-sensitized photoelectrosynthesis cells and other applications. Disclosed herein are self-assembled multilayers as a strategy for manipulating electron transfer dynamics at these interfaces. The multilayer films are achieved by stepwise layering of bridging molecules, linking ions, and active molecule on an oxide surface. The formation of the proposed architecture is supported by ATR-IR and UV-Vis spectroscopy. Time-resolved emission and transient absorption establishes that the films exhibit an exponential decrease in electron transfer rate with increasing bridge length. The findings indicate that self-assembled multilayers offer a simple, straight forward and modular method for manipulating electron transfer dynamics at dye-oxide interfaces.

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