By using a facile one-pot nucleophilic addition reaction, we synthesized a novel imidazole (IMZ)-functionalized fullerene (C-IMZ), and applied it as a third component of inverted ternary polymer solar cells (PSCs), leading to dramatic efficiency enhancement. According to FT-IR, XPS spectroscopic characterizations, and elemental analysis, the chemical structure of C-IMZ was determined with the average IMZ addition number estimated to be six. The lowest unoccupied molecular orbital (LUMO) level of C-IMZ measured by cyclic voltammetry was -3.63 eV, which is up-shifted relative to that of 6,6-phenyl C-butyric acid methyl ester (PCBM). Upon doping C-IMZ as a third component into an active layer blend of poly(3-hexylthiophene) (P3HT) and PCBM, the power conversion efficiency (PCE) of the inverted ternary PSCs was 3.4% under the optimized doping ratio of 10 wt %, dramatically higher than that of the control device ITO/P3HT:PCBM/MoO/Ag based on the binary P3HT:PCBM blend (1.3%). The incorporation of C-IMZ results in enhancement of the absorption of P3HT:PCBM blend film, increase of the electron mobility of the device, and rougher film surface of the P3HT:PCBM active layer beneficial for interfacial contact with the Ag anode. Furthermore, C-IMZ doped in P3HT:PCBM blend may migrate to the surface of ITO cathode via vertical phase separation as revealed by XPS depth analysis, consequently forming a cathode interfacial layer (CIL), which can lower the work function (WF) of ITO cathode. Thus, the interfacial contact between the active layer and ITO cathode is improved, facilitating electron transport from the active layer to ITO cathode. The effectiveness of C-IMZ as a vertically phase-separated CIL on efficiency enhancement of inverted ternary PSCs is further verified by doping it into another active layer system comprised of a low-bandgap conjugated polymer, poly(thieno[3,4-b]-thiophene/benzodithiophene) (PTB7), blended with [6,6]-phenyl C-butyric acid methyl ester (PCBM). Under the optimized C-IMZ doping ratio of 10 wt %, the PCE of the PTB7:PCBM-based inverted ternary PSC device reaches 5.3%, which is about 2 times higher than that of the control binary device (2.6%).
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http://dx.doi.org/10.1021/acsami.6b13461 | DOI Listing |
Nanoscale
January 2025
School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Circularly polarized luminescence (CPL) materials with precisely controlled emission colors and handedness are highly desirable for their promising applications in advanced optical technologies, but it is rather challenging to obtain them primarily due to the lack of convenient, powerful, and universal preparation strategies. Herein, we report a simple yet versatile solution route for constructing multicolor CPL materials with controllable handedness from nonchiral luminescent charge-transfer (CT) complexes through co-assembly with chiral N-terminal aromatic amino acids. The resulting ternary co-assemblies exhibit obvious CPL signals from 489 to 601 nm, covering from blue green and yellow to orange-red.
View Article and Find Full Text PDFAdv Mater
December 2024
School of Physics, State Key Laboratory of Crystal Materials, Shandong University, Jinan, Shandong, 250100, P. R. China.
Developing stable and highly efficient thick-film organic solar cells (OSCs) is crucial for the large-scale commercial application of organic photovoltaics. A novel synergistic dilution strategy to address this issue, using Polymethyl Methacrylate (PMMA) -modified zinc oxide (ZnO) as the interfacial layer, is introduced. This strategy effectively mitigates oxygen defects in ZnO while also regulating the self-assembly process of the active layer to achieve an ordered distribution of donors and acceptors.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2024
School of Physics and Electronic Information, Yantai University, Yantai 264005, China.
In this study, we developed a flexible cathode for fabricating high-performance ternary organic solar cells (OSCs). With solvent engineering and acid treatment, the conductivity of the poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) electrode was significantly enhanced with the sheet resistance reduced from 1081 to 83 Ω sq. After being coated with polyethylenimine, work function of the PEDOT:PSS electrode was tuned from -5.
View Article and Find Full Text PDFSmall
October 2024
State Key Laboratory of Luminescent Materials and Devices, Institute of Polymer Optoelectronic Materials and Devices, Guangdong Basic Research Center of Excellence for Energy & Information Polymer Materials, South China University of Technology, 381 Wushan Road, Guangzhou, 510640, China.
Inverted organic solar cells (OSCs) have garnered significant interest due to their remarkable stability. In this study, the efficiency and stability of inverted OSCs are enhanced via the in situ self-organization (SO) of an interfacial modification material Phen-NaDPO onto tin oxide (SnO). During the device fabrication, Phen-NaDPO is spin-coated with the active materials all together on SnO.
View Article and Find Full Text PDFNanoscale
May 2024
School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Handedness inversion of supramolecular chirality and circularly polarized luminescence (CPL) in assembled systems containing more than two components with higher complexity is of prominent importance to simulate biological multicomponent species and design advanced chiral materials, but it remains a considerable challenge. Herein, we have successfully developed ternary co-assembly systems based on aromatic amino acids, vinylnaphthalene derivatives and 1,2,4,5-tetracyanobenzene with effective chirality transfer. Notably, the handedness of supramolecular chirality and CPL can be readily inverted by changing the residues of amino acids, the substituents of achiral vinylnaphthalene derivatives, or by adjusting the stoichiometric ratio.
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