Ultrafast Energy Transfer in Ultrathin Organic Donor/Acceptor Blend

被引:34
|
作者
Kandada, Ajay Ram Srimath [1 ,2 ]
Grancini, Giulia [2 ]
Petrozza, Annamaria [2 ]
Perissinotto, Stefano [2 ]
Fazzi, Daniele [2 ]
Raavi, Sai Santosh Kumar [2 ]
Lanzani, Guglielmo [1 ,2 ]
机构
[1] Univ Milan, Dipartimento Fis, I-20133 Milan, Italy
[2] Ist Italiano Tecnol, Ctr Nano Sci & Technol PoliMi, I-20133 Milan, Italy
来源
SCIENTIFIC REPORTS | 2013年 / 3卷
关键词
EXCITATION TRANSFER; RATE EXPRESSIONS; CARRIER GENERATION; CHARGE GENERATION; SOLAR-CELLS; MORPHOLOGY; DYNAMICS; FILMS; ELECTRON; DONORS;
D O I
10.1038/srep02073
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is common knowledge that poly(3-hexylthiophene) (P3HT)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) blend, a prototype system for bulk heterojunction (BHJ) solar cells, consists of a network of tens of nanometers-large donor-rich and acceptor-rich phases separated by extended finely intermixed border regions where PCBM diffuse into P3HT. Here we specifically address the photo-induced dynamics in a 10 nm thin P3HT/PCBM blend that consists of the intermixed region only. Using the multi-pass transient absorption technique (TrAMP) that enables us to perform ultra high sensitive measurements, we find that the primary process upon photoexcitation is ultrafast energy transfer from P3HT to PCBM. The expected charge separation due to hole transfer from PCBM to P3HT occurs in the 100 ps timescale. The derived picture is much different from the accepted view of ultra-fast electron transfer at the polymer/PCBM interface and provides new directions for the development of efficient devices.
引用
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页数:7
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