Here, we report incorporation of multiwalled carbon nanotubes (MWNTs) in Poly(3-octylthiophene)/fullerene heterojunction solar cells. Multi-walled carbon nanotubes (MWNTs) were functionalized by oxygen plasma treatment. Photoelectron spectroscopy study of oxygen plasma treated MWNTs shows surface modification with hydroxyl and carboxyl groups. Plasma treated MWNTs were combined with Poly(3-octylthiophene) and solar cell was fabricated with the structure Au/P3OT + MWNTs/C60/FTO. Fabricated device shows short circuit current density (Jsc) open circuit voltage (Voc), fill factor and conversion efficacy as 0.04 mA/cm2, 0.355 V, 21% and 0.003%. Solar cell fabricated with incorporation of MWNTs shows much better device performance, then that of the device without MWNTs. MWNTs in the polymer composite act as exciton dissociation site and provide efficient hole transportation, and thereby improving device performance.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1166/jnn.2010.1974 | DOI Listing |
Langmuir
January 2025
Surface Science Laboratory, Graduate School of Engineering, Toyota Technological Institute, 2-12-1, Hisakata, Tempaku, Nagoya, Aichi 468-8511, Japan.
Hydrogen-substituted graphdiyne (HsGDY) is a two-dimensional material with an sp-sp carbon skeleton featuring a band gap and a porous structure that enhances ion diffusion. In previous reports, HsGDY growth was limited to metal substrates such as Cu, which then required transfer. Here, we developed a sandwich method that allows HsGDY to be grown directly on the target substrate.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan.
The development of hole-collecting materials is indispensable to improving the performance of perovskite solar cells (PSCs). To date, several anchorable molecules have been reported as effective hole-collecting monolayer (HCM) materials for p-i-n PSCs. However, their structures are limited to well-known electron-donating skeletons, such as carbazole, triarylamine, etc.
View Article and Find Full Text PDFScience
January 2025
Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, China.
Emerging wearable devices would benefit from integrating ductile photovoltaic light-harvesting power sources. In this work, we report a small-molecule acceptor (SMA), also known as a non-fullerene acceptor (NFA), designed for stretchable organic solar cell (-OSC) blends with large mechanical compliance and performance. Blends of the organosilane-functionalized SMA BTP-Si4 with the polymer donor PNTB6-Cl achieved a power conversion efficiency (PCE) of >16% and ultimate strain (ε) of >95%.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
College of Physics Science and Technology, Hebei University, Baoding 071002, China.
Developing the Cd-free electron transport layer (ETL) is a crucial subject in the field of antimony selenide (SbSe) solar cells. At present, the power conversion efficiency (PCE) of the Cd-free SbSe solar cell is still substantially lower than that of CdS-based devices. It is significant to reveal the electron transfer features in SbSe/CdS heterojunction and SbSe/Cd-free ETL heterojunction for development of a Cd-free SbSe solar cell with high PCE.
View Article and Find Full Text PDFACS Nano
January 2025
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, LIFM, School of Chemistry, IGCME, Sun Yat-Sen University, Guangzhou 510275, China.
Perovskite solar cells (PSCs) have emerged as low-cost photovoltaic representatives. Constructing three-dimensional (3D)/two-dimensional (2D) perovskite heterostructures has been shown to effectively enhance the efficiency and stability of PSCs. However, further enhancement of device performance is still largely limited by inferior conductivity of the 2D perovskite capping layer and its mismatched energy level with the 3D perovskite layer.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!