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Transient Photocurrent Response of Plasmon-Enhanced Polymer Solar Cells with Gold Nanoparticles

In this work, the transient photocurrent of the plasmon-enhanced polymer bulk heterojunction solar cells based on poly(3-hexylthiophene) (P3HT) and [6,6]-Phenyl C(61) butyric acid methyl ester (PCBM) is investigated. Two kinds of localized surface plasmon resonance (LSPR) enhanced devices were fabri...

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Detalles Bibliográficos
Autores principales: Fang, Yi, Hou, Yanbing, Hu, Yufeng, Teng, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455668/
https://www.ncbi.nlm.nih.gov/pubmed/28793424
http://dx.doi.org/10.3390/ma8074050
Descripción
Sumario:In this work, the transient photocurrent of the plasmon-enhanced polymer bulk heterojunction solar cells based on poly(3-hexylthiophene) (P3HT) and [6,6]-Phenyl C(61) butyric acid methyl ester (PCBM) is investigated. Two kinds of localized surface plasmon resonance (LSPR) enhanced devices were fabricated by doping the gold nanoparticles (Au NPs) into the anode buffer layer and inserting Au NPs between the anode buffer layer and the active layer. We probed the dynamics of the turn-on and turn-off responses to 400 μs square-pulse optical excitation from the 380 nm and 520 nm light-emitting diodes (LED) driven by an electric pulse generator. The transient photocurrent curves of devices with Au NPs at different positions and under different excitation wavelength are compared and analyzed. The charge trapping/detrapping processes that occurred at the interface of Au NPs and the active layer were observed; these exhibit an overshoot in the initial fast rise of photocurrent response. Our results show that the incorporating position of Au NPs is an important key factor to influence the transient photocurrent behaviors.