Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 17, Issue 45, Pages 30712-30720Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cp05557a
Keywords
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Funding
- Fundamental Research Funds for the Central Universities [2015YJS176]
- National Natural Science Foundation of China [61377029]
- Beijing Natural Science Foundation [2122050]
- National Science Foundation [CMM-1265834]
- one hundred talents project of Beijing Jiaotong University
- Div Of Civil, Mechanical, & Manufact Inn
- Directorate For Engineering [1265834] Funding Source: National Science Foundation
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We report polymer photodetectors (PPDs) with an evident photomultiplication (PM) phenomenon, based on a sandwich structure ITO/PEDOT: PSS/P3HT:PC71BM(100:1)/Al. A similar device structure has been reported in our previous work, showing great potential as a new type of high performance PPD. However, we found more interesting new phenomena from these PPDs. Solid evidence is provided to prove the existence of photogenerated electron transport in the almost hole-only active layer under an applied bias. The transport of photogenerated electrons leads to electron accumulation near the Al electrode and the electron redistribution, which strongly affect the EQE spectral shape and the transient response of the PPDs. Our conclusion is further confirmed by confirmatory devices with a structure of Al(1)/P3HT:PC71BM(100:1)/Al(2). EQE spectra and transient J(ph) curves of the confirmatory devices accord well with our speculation. This discovery may provide a new insight to increase the response speed of PM type PPDs by adjusting the photogenerated electron distribution in the active layer. Considering that the PM type PPDs have much higher EQE than the traditional organic photodetectors, the improvement may further extend its potential applications with low cost.
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