Efficient light emission from inorganic and organic semiconductor hybrid structures by energy-level tuning
The fundamental limits of inorganic semiconductors for light emitting applications, such as holographic displays, biomedical imaging and ultrafast data processing and communication, might be overcome by hybridization with their organic counterparts, which feature enhanced frequency response and colo...
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Veröffentlicht in: | Nature communications 2015-04, Vol.6 (1), p.6754-6754, Article 6754 |
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Sprache: | eng |
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Zusammenfassung: | The fundamental limits of inorganic semiconductors for light emitting applications, such as holographic displays, biomedical imaging and ultrafast data processing and communication, might be overcome by hybridization with their organic counterparts, which feature enhanced frequency response and colour range. Innovative hybrid inorganic/organic structures exploit efficient electrical injection and high excitation density of inorganic semiconductors and subsequent energy transfer to the organic semiconductor, provided that the radiative emission yield is high. An inherent obstacle to that end is the unfavourable energy level offset at hybrid inorganic/organic structures, which rather facilitates charge transfer that quenches light emission. Here, we introduce a technologically relevant method to optimize the hybrid structure’s energy levels, here comprising ZnO and a tailored ladder-type oligophenylene. The ZnO work function is substantially lowered with an organometallic donor monolayer, aligning the frontier levels of the inorganic and organic semiconductors. This increases the hybrid structure’s radiative emission yield sevenfold, validating the relevance of our approach.
Hybrid inorganic-organic structures can overcome the limits of inorganic semiconductor light emitting devices but the energy level offset is an obstacle. Here, Schlesinger
et al.
lower the ZnO work function with an organometallic donor monolayer and enhance the radiative emission of the hybrid structure. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms7754 |