The implementation of positive alternative electron transporting layers (ETLs) with excellent electronic properties is a most promising method to up-scale low-cost highly efficient perovskite solar cell (PSC) technology. The present work demonstrates the preparation of tin oxide (SnO2) nanofibers (NF) and nanobelts (NB) as an electron transporting layer (ETL) for PSCs. The smooth and uniform nanofibers and nanobelts have been prepared using an electrospinning technique followed by calcination at 600 °C. Thermogravimetric analysis (TGA) analysis performed on the as-spun polyvinylpyrrolidone-tin oxide (PVP-SnO2) composite suggests that a calcination temperature of 600 °C is required to obtain pure SnO2 and to ensure complete removal of PVP along with other organic solvents. The structural analysis confirmed the presence of the pure tetragonal rutile phase of SnO2 nanofibers and nanobelts. The prepared nanofibers and nanobelts were further used as ETLs for PSCs. Our optimized experimental parameters yielded a JSC of 22.46 mA cm-2, a VOC of 1.081 V and FF of 66%, leading to >16% power conversion efficiency (PCE) for SnO2 nanobelts using an (FAPbI3)0.85(MAPbI3)0.15 perovskite absorber layer with good stability. The obtained PCE is much higher than that of the SnO2 NF (12.893%) morphology. Nevertheless, the synthesis of SnO2 NF/NB ETLs provides a simple, low-cost and large-scale method for PSCs.
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http://dx.doi.org/10.1039/c8nr00695d | DOI Listing |
RSC Adv
October 2024
Chemical Engineering Department, Faculty of Engineering, Minia University Minia 61516 Egypt +20862364420 +20862348005.
Sensors (Basel)
September 2024
Faculty of Electronics, Photonics and Microsystems, Wrocław University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50-370 Wroclaw, Poland.
Metal oxide core-shell fibrous nanostructures are promising gas-sensitive materials for the detection of a wide variety of both reducing and oxidizing gases. In these structures, two dissimilar materials with different work functions are brought into contact to form a coaxial heterojunction. The influence of the shell material on the transportation of the electric charge carriers along these structures is still not very well understood.
View Article and Find Full Text PDFAdv Sci (Weinh)
April 2024
State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, Jiangsu Engineering Laboratory of Novel Functional Polymeric Materials, Suzhou Key Laboratory of Macromolecular Design and Precision Synthesis, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, China.
New insights are raised to interpret pathway complexity in the supramolecular assembly of chiral triarylamine tris-amide (TATA) monomer. In cosolvent systems, the monomer undergoes entirely different assembly processes depending on the chemical feature of the two solvents. Specifically, 1,2-dichloroethane (DCE) and methylcyclohexane (MCH) cosolvent trigger the cooperative growth of monomers with M helical arrangement, and hierarchical thin nanobelts are further formed.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2023
Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou 450052, China.
The fabrication of chiral thin films with tunable circularly polarized luminescence (CPL) colors is important in developing chiroptical materials but remains challenging due to the lack of assembly-initiated chiral film formation methodology. Here, by adopting a combined solution aggregation and interfacial assembly strategy, we report the fabrication of chiral film materials with full-color and white-light CPL. A biquinoline glutamic acid ester (abbreviated as BQGE) shows a typical aggregation-induced emission property with blue CPL after solution aggregation.
View Article and Find Full Text PDFSci Rep
May 2023
Department of Physics, Faculty of Science, University of Guilan, Namjoo Avenue, P.O. Box 4193833697, Rasht, Iran.
Ni-incorporated MgFeO (MgNiFeO) porous nanofibers were synthesized using the sol-gel electrospinning method. The optical bandgap, magnetic parameters, and electrochemical capacitive behaviors of the prepared sample were compared with pristine electrospun MgFeO and NiFeO based on structural and morphological properties. XRD analysis affirmed the cubic spinel structure of samples and their crystallite size is evaluated to be less than 25 nm using the Williamson-Hall equation.
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