Suchergebnisse

Voltage losses in singlet material-based organic photovoltaic devices (OPVs) have been intensively studied, whereas, only a few investigations on triplet material-based OPVs (T-OPVs) are reported. To investigate the voltage loss in T-OPVs, two homoleptic iridium(iii) complexes based on extended pi-conjugated benzo[g]phthalazine ligands, Ir(Ftbpa)(3) and Ir(FOtbpa)(3), are synthesized as sole electron donors. T-OPVs are fabricated by mixing two donors with phenyl-C-71-butyric acid methyl ester (PC71BM) as an electron acceptor. Insertion of oxygen-bridges as flexible inert delta-spacers in Ir(FOtbpa)(3) has slightly elevated both the lowest unoccupied molecular orbital and the highest occupied molecular orbital levels compared to those of Ir(Ftbpa)(3), which results in a lower charge transfer (CT) state energy (E-CT) for Ir(FOtbpa)(3)-based devices. However, a higher V-oc (0.88 V) is observed for Ir(FOtbpa)(3)-based devices than those of Ir(Ftbpa)(3) (0.80 V). To understand the above result, the morphologies of the two blend films are studied, which excludes the influence of morphology. Furthermore, radiative and non-radiative recombination in two devices is quantitatively investigated, which suggests that a higher V-oc can be attributed to reduced radiative and non-radiative recombination loss for the Ir(FOtbpa)(3)-based devices. ; Funding Agencies|Swedish Foundation for International Cooperation in Research and Higher Education (STINT); Knut and Alice Wallenberg foundationKnut & Alice Wallenberg Foundation [2016.0059]; Swedish Government Research Area in Materials Science on Functional Materials at Linkoping University [200900971]; China Scholarship Council (CSC)China Scholarship Council; NSFC of ChinaNational Natural Science Foundation of China [51711530040, 51473086]; National Postdoctoral Program for Innovative Talents [BX20180159]

Organic photovoltaic cells (OPVs) have attracted broad attention and become a very energetic field after the emergence of nonfullerene acceptors. Long-lifetime triplet excitons are expected to be good candidates for efficiently harvesting a photocurrent. Parallel with the development of OPVs based on singlet materials (S-OPVs), the potential of triplet materials as photoactive layers has been explored. However, so far, OPVs employing triplet materials in a bulk heterojunction have not exhibited better performance than S-OPVs. Here, the recent progress of representative OPVs based on triplet materials (T-OPVs) is briefly summarized. Based on that, the performance limitations of T-OPVs are analyzed. The shortage of desired triplet materials with favorable optoelectronic properties for OPVs, the tradeoff between long lifetime and high binding energy of triplet excitons, as well as the low charge mobility in most triplet materials are crucial issues restraining the efficiencies of T-OPVs. To overcome these limitations, first, novel materials with desired optoelectronic properties are urgently demanded; second, systematic investigation on the contribution and dynamics of triplet excitons in T-OPVs is necessary; third, close multidisciplinary collaboration is required, as proved by the development of S-OPVs. ; Funding Agencies|Knut and Alice Wallenberg foundation [2016.0059]; STINT funds for the Joint China-Sweden Mobility programme; Swedish Government Research Area in Materials Science on Functional Materials at Linkoping University Faculty Grant SFO-Mat-LiU [200900971]; China Scholarship Council (CSC); NSFC of China [51711530040, 51473086, 51773207, 91633301]; MOST [2017YFA0204702, 2018YFA0208504]