Post-Deposition Activation of Latent Hydrogen-Bonding: A New Paradigm for Enhancing the Performances of Bulk Heterojunction Solar Cells

被引:29
|
作者
Bruni, Francesco [1 ]
Sassi, Mauro [1 ]
Campione, Marcello [2 ]
Giovanella, Umberto [3 ]
Ruffo, Riccardo [1 ]
Luzzati, Silvia [3 ]
Meinardi, Francesco [1 ]
Beverina, Luca [1 ]
Brovelli, Sergio [1 ]
机构
[1] Univ Milano Bicocca, Dipartimento Sci Mat, I-20125 Milan, Italy
[2] Univ Milano Bicocca, Dipartimento Sci Ambiente & Terr Sci Terra, I-20125 Milan, Italy
[3] Consiglio Nazl Ric ISMac CNR, Ist Studio Macromol, I-20133 Milan, Italy
关键词
FIELD-EFFECT TRANSISTORS; ORGANIC PHOTOVOLTAICS; CHARGE-TRANSPORT; CONJUGATED POLYMERS; IMPROVED EFFICIENCY; THIN-FILMS; DIKETOPYRROLOPYRROLE; MORPHOLOGY; PIGMENTS; MOBILITY;
D O I
10.1002/adfm.201400896
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Small conjugated molecules (SM) are gaining momentum as an alternative to semiconducting polymers for the production of solution-processed bulk heterojunction (BHJ) solar cells. The major issue with SM-BHJs is the low carrier mobility due to the scarce control on the phase-segregation process and consequent lack of preferential percolative pathways for electrons and holes to the extraction electrodes. Here, a new paradigm for fine tuning the phase-segregation in SM-BHJs, based on the post-deposition exploitation of latent hydrogen bonding in binary mixtures of PCBM with suitably functionalized electron donor molecules, is demonstrated. The strategy consist in the chemical protection of the H-bond forming sites of the donor species with a thermo-labile functionality whose controlled thermal cleavage leads to the formation of stable, crystalline, phase-separated molecular aggregates. This approach allows the fine tuning of the nanoscale film connectivity and thereby to simultaneously optimize the generation of geminate carriers at the donor-acceptor interfaces and the extraction of free charges via ordered phase-separated domains. As a result, the PV efficiency undergoes an over twenty-fold increase with respect to control devices. This strategy, demonstrated here with mixtures of diketopyrrolopyrrole derivatives with PCBM can be extended to other molecular systems for achieving highly efficient SM-BHJ solar cells.
引用
收藏
页码:7410 / 7419
页数:10
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