Poly(4-vinylpyridine) (P4VP) was used as a cathode interface layer in inverted organic solar cells (OSCs) fabricated using poly[2,3-bis(3-octyloxyphenyl)quinoxaline-5,8-diyl-alt-thiophene-2,5-diyl] (TQ1) and PCBM (phenyl C butyric acid methyl ester) as the donor and acceptor materials, respectively. We successfully demonstrate that the work function of underlying indium tin oxide (ITO) electrode can be significantly reduced by ∼0.7 eV, after modification of the surface with a thin film of P4VP. Photoconversion efficiency of 4.7% was achieved from OSCs incorporating P4VP interface layer between the ITO and bulk heterojunction (BHJ). Thin P4VP layer, when used to modify ZnO electron transport layer in inverted OSCs, reduced the ZnO work function from 3.7 to 3.4 eV, which resulted in a noteworthy increase in open-circuit voltage from 840 to 890 mV. On simultaneous modification of ZnO with P4VP and optimization of the BHJ morphology by using solvent additive chloronapthalene, photoconversion efficiency of OSCs was significantly increased from 4.6% to 6.3%. The enhanced device parameters are also attributed to an energetically favorable material stratification, as a result of an enrichment of PCBM toward the P4VP interface.
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http://dx.doi.org/10.1021/acsami.6b12687 | DOI Listing |
Sci Rep
January 2025
Faculty of Physics, Warsaw University of Technology, 75 Koszykowa Str., 00-662, Warszawa, Poland.
Surface relief grating formation in photo-responsive azo polymers under irradiation is a long-ago-found phenomenon, but all the factors governing its efficiency are still not fully recognized. Here, we report on the enormous impact of the polymer thickness on the possibility of fabrication of extremely high-amplitude surface deformations. We performed prolonged holographic recordings on the layers of the same azobenzene poly(ether imide), which had substantially different optical transmittances at the recording wavelength and revealed that the depths of the inscribed relief structures increased with the polymer thickness from a nondetectable value up to almost 2 µm, unaffected by the presence of a polymer-glass substrate interface in either sample.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Multiscale Computational Materials Facility & Materials Genome Institute, School of Materials Science and Engineering, Fuzhou University, Fuzhou 350108, PR China. Electronic address:
Localized high-concentration electrolytes (LHCEs) offer a new methodology to improve the functionality of conventional electrolytes. Understanding the impact of antisolvents on bulk electrolytes is critical to the construction of sophisticated LHCEs. However, the mechanism of how antisolvent modulates the electrochemical reactivity of the solvation structure in LHCEs remains unclear.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Department of Mechanical Engineering, University of Alberta, 9211-116 Street NW., Edmonton, Alberta T6G 1H9, Canada. Electronic address:
Copper hexacyanoferrate (CuHCF) demonstrates high working voltage, convenient synthesis methods, and economic benefits. However, capacity decay of CuHCF//Zn full cells is usually observed in aqueous electrolytes due to the dissolution of Cu and Fe, as indicated by the irreversible insertion of Zn ions and the consequent formation of ZnCuHCF. To address these challenges, a cathode-oriented electrolyte engineering design employing a methyl acetate (MA) co-solvent with zinc triflate (Zn(OTf)) salt electrolyte is implemented.
View Article and Find Full Text PDFNanotechnology
January 2025
MME, Wright State University, 3640 Colonel Glenn Hwy, Lake Campus, 7600 Lake Drive, Lake Campus, Fairborn, Ohio, 45435, UNITED STATES.
Surface induced crystallization/amorphization of a Germanium-antimony-tellurium (GST) nanolayer is investigated using the phase field model. A Ginzburg-Landau (GL) equation introduces an external surface layer (ESL) within which the surface energy and elastic properties are properly distributed. Next, the coupled GL and elasticity equations for the crystallization/amorphization are solved.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Low-temperature proton exchange membrane fuel cells (PEMFCs) reuqire highly pure hydrogen gas due to their extreme sensitivity to carbon monoxide (CO) contamination, which poses a challenge for using cost-effective reformed hydrogen sources. To address this issue, we have developed a surface modification strategy by applying a 0.5-0.
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