To maximize light coupling into the active layer, plasmonic nanostructures have been incorporated into both active layers of organic solar cells (OSCs) and perovskite solar cells (PSCs) with the aim of increasing light absorption, but reports have shown controversial results in electrical characteristics. In this work, we introduce a core-bishell concept to build plasmonic nanoparticles (NPs) with metal-inorganic semiconductor-organic semiconductor nanostructure. Specifically, Ag NPs were decorated with a titania/benzoic-acid-fullerene bishell (Ag@TiO@Pa), which enables the NPs to be compatible with fullerene acceptors or a perovskite absorber. Moreover, coating the Ag@TiO NP with a fullerene shell can activate efficient plasmon-exciton coupling and eliminate the charge accumulation, thus facilitating exciton dissociation and reducing the monomolecular recombination. The improved light absorption and enhanced carrier extraction of devices with Ag@TiO@Pa nanoparticles are responsible for the improved short-circuit current and fill factor, respectively. On the basis of the synergistic effects (optical and electrical), a series of plasmonic OSCs exhibited enhancement of 12.3-20.7% with a maximum power conversion efficiency of 13.0%, while the performance of plasmonic PSCs also showed an enhancement by 10.2% from 18.4% to 20.2%. This core-bishell design concept of plasmonic nanostructures demonstrates a general approach to improving the photovoltaic performance with both optical and electrical contributions.
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http://dx.doi.org/10.1021/acsnano.9b00135 | DOI Listing |
Angew Chem Int Ed Engl
March 2025
South China University of Technology, State Key Laboratory of Luminescent Materials and Devices, Wushan Road 381, 510640, Guangzhou, CHINA.
Energy loss (Eloss) between optical energy gap (Eg) and open-circuit voltage (eVoc) sets efficiency upper limits for organic solar cells (OSCs). Nevertheless, further breaking the limit of Eloss in OSCs is challenging, especially via structurally simple materials in binary OSCs. Herein, a structurally simple non-halogenated polymer donor, namely PBDCT, is developed for realizing high-efficiency OSCs with record-breaking Eloss.
View Article and Find Full Text PDFACS Appl Mater Interfaces
March 2025
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, China.
Developing vapor-solid reaction methods to prepare organic-inorganic hybrid perovskite thin films is highly compatible with processes in crystalline silicon solar cells and the thin-film photovoltaic industries, facilitating rapid industrialization. In the vapor-solid reaction, the crystallization quality of perovskite thin films is widely influenced by the crystallinity and microstructure of lead iodide (PbI) precursor films. During the thermal evaporation process of preparing the PbI precursor films, we observed that PbI tends to develop a disordered surface morphology and exhibits high crystallinity, which significantly hinders the uniform diffusion of the organic amine salt vapor during the subsequent vapor-solid reaction.
View Article and Find Full Text PDFWe report the cosolvency effect of formamidinium lead triiodide (FAPbI) in a mixture of γ-butyrolactone (GBL) and 2-methoxyethanol (2ME), a phenomenon where FAPbI shows higher solubility in the solvent blend than in either alone. We found that FAPbI exhibits 10× higher solubility in 30% 2ME in GBL than in 2ME alone and 40% higher solubility than in GBL alone at 90 °C. This enhanced solubility is attributed to the disruption of the hydrogen bonding network within 2ME, allowing its hydroxyl and ether groups to interact more freely with the solute.
View Article and Find Full Text PDFOrg Lett
March 2025
Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-Based Materials, and School of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241002, People's Republic of China.
The Cu(II)-catalyzed -heteroannulation reaction of [60]fullerene (C) with aryl sulfonamides and paraformaldehyde has been disclosed for the synthesis of diverse C-fused imidazolidines, of which one or both of the ArSO moieties could be removed selectively. Further transformations into the unexpected bicyclic 1,2,3,4-adduct and C-fused imidazolidinium iodide salt have also been demonstrated. A plausible reaction mechanism is proposed on the basis of control experiments.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290, United States.
Semiconductor devices often rely on high-purity materials and interfaces achieved through vapor- and vacuum-based fabrication methods, which can enable precise compositional control down to single atomic layers. Compared to groups IV and III-V semiconductors, hybrid perovskites (HPs) are an emergent class of semiconductor materials with remarkable solution processability and compositional variability that have facilitated rapid experimentation to achieve new properties and progress toward efficient devices, particularly for solar cells. Surprisingly, vapor deposition techniques for HPs are substantially less developed, despite the complementary benefits that have secured vapor methods as workhorse tools for semiconductor fabrication.
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