The insertion of a DNA nanolayer into polymer based solar cells, between the electron transport layer (ETL) and the active material, is proposed to improve the charge separation efficiency. Complete bulk heterojunction donor–acceptor solar cells of the layered type glass/electrode (indium tin oxide)/ETL/P3HT:PC 70 BM/hole transport layer/electrode (Ag) are investigated using femtosecond transient absorption spectroscopy both in the NIR and the UV–vis regions of the spectrum. The transient spectral changes indicate that when the DNA is deposited on the ZnO nanoparticles (ZnO-NPs) it can imprint a different long range order on the poly(3-hexylthiophene) (P3HT) polymer with respect to the non-ZnO-NPs/DNA containing cells. This leads to a larger delocalization of the initially formed exciton and its faster quenching which is attributed to more efficient exciton dissociation. Finally, the temporal response of the NIR absorption shows that the DNA promotes more efficient production of charge transfer states and free polarons in the P3HT cation indicating that the increased exciton dissociation correlates with increased charge separation.
Toschi, F., Catone, D., O'Keeffe, P., Paladini, A., Turchini, S., Dagar, J., et al. (2018). Enhanced Charge Separation Efficiency in DNA Templated Polymer Solar Cells. ADVANCED FUNCTIONAL MATERIALS, 28(26), 1707126 [10.1002/adfm.201707126].
Enhanced Charge Separation Efficiency in DNA Templated Polymer Solar Cells
Toschi, Francesco;Dagar, Janardan;Brown, Thomas M.
2018-01-01
Abstract
The insertion of a DNA nanolayer into polymer based solar cells, between the electron transport layer (ETL) and the active material, is proposed to improve the charge separation efficiency. Complete bulk heterojunction donor–acceptor solar cells of the layered type glass/electrode (indium tin oxide)/ETL/P3HT:PC 70 BM/hole transport layer/electrode (Ag) are investigated using femtosecond transient absorption spectroscopy both in the NIR and the UV–vis regions of the spectrum. The transient spectral changes indicate that when the DNA is deposited on the ZnO nanoparticles (ZnO-NPs) it can imprint a different long range order on the poly(3-hexylthiophene) (P3HT) polymer with respect to the non-ZnO-NPs/DNA containing cells. This leads to a larger delocalization of the initially formed exciton and its faster quenching which is attributed to more efficient exciton dissociation. Finally, the temporal response of the NIR absorption shows that the DNA promotes more efficient production of charge transfer states and free polarons in the P3HT cation indicating that the increased exciton dissociation correlates with increased charge separation.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
