Elucidating the photoluminescence-enhancement mechanism in a push-pull conjugated polymer induced by hot-electron injection from gold nanoparticles

被引:13
|
作者
Lee, Dongki [1 ]
Han, Se Gyo [2 ]
Mun, Jungho [2 ]
Yang, Kihyuk [1 ]
Kim, Sung Hyuk [1 ]
Rho, Junsuk [2 ,3 ]
Cho, Kilwon [2 ]
Oh, Dongyeop X. [4 ]
Jeong, Mun Seok [1 ]
机构
[1] Sungkyunkwan Univ, Dept Energy Sci, Suwon 16419, South Korea
[2] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 37673, South Korea
[3] Pohang Univ Sci & Technol, Dept Mech Engn, Pohang 37673, South Korea
[4] Korea Res Inst Chem Technol KRICT, Res Ctr Biobased Chem, Ulsan 44429, South Korea
基金
新加坡国家研究基金会;
关键词
RESONANCE ENERGY-TRANSFER; SOLAR-CELLS; OPTICAL-PROPERTIES; PLASMON RESONANCE; METAL; EFFICIENCY; DYNAMICS; NANOSTRUCTURES; RELAXATION; NANOFIBERS;
D O I
10.1364/PRJ.409762
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Understanding the photophysical interactions between the components in organic-inorganic nanocomposites is a key factor for their efficient application in optoelectronic devices. In particular, the photophysical study of nanocomposites based on organic conjugated polymers is rare. We investigated the effect of surface plasmon resonance (SPR) of gold nanoparticles (Au NPs) on the photoluminescence (PL) property of a push-pull conjugated polymer (PBDB-T). We prepared the hybrid system by incorporating poly(3-hexylthiophene)-stabilized Au NPs (P3HT-Au NPs) into PBDB-T. The enhanced and blueshifted PL was observed in the hybrid system compared to PL in a neat PBDB-T system, indicating that the P3HT chains attached to the Au NPs suppressed charge-transfer from PBDB-T to the Au NPs and relayed the hot electrons to PBDB-T (the band-filling effect). This photophysical phenomenon limited the auto-dissociation of PBDB-T eadtons. Thus, the radiative recombination of the excitons occurred more in our hybrid system than in the neat system. (C) 2021 Chinese Laser Press
引用
收藏
页码:131 / 141
页数:11
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