ABSTRACT
Fly ash solid waste from a power plant was applied in a solar cell application for the first time. A doctor blade was used to coat FTO-glass with a composite film of mixed fly ash and PEDOT:PSS (FP). XRD, FTIR, SEM, EDX, and BET analyses were used to elucidate the crystal structure, morphology, and functional groups of fly ash in the current research. A significantly high efficiency solar cell was fabricated utilizing fly ash. CV, Tafel, and EIS analyses indicated a decrease in charge transfer resistance and an increased catalytic activity in the counter electrodes. The performance of DSSCs made from FP counter electrodes varied depending on the percentage of fly ash particles present. Fly ash mixed with PEDOT:PSS in a concentration ratio of 2:5 g/mL showed a high efficiency of 4.23%, which is comparable to Pt DSSC's (4.84%). Moreover, FP-2:5 presented a more highly efficient electrode than counter electrodes made from PEDOT:PSS mixed with MoO (3.08%) and CoO (3.65%). This suitability of this low-cost CE material for use in DSSCs has been established.
ABSTRACT
RT ferromagnetism was observed in nanoparticles of Fe-doped CeO2 (i.e., Ce(0.97)Fe(0.03)O2) synthesized by a sol-gel method. The undoped and Fe-doped CeO2 were characterized by XRD, Raman spectroscopy, TEM, and VSM. The undoped samples and Ce(0.97)Fe(0.03)O2 precursor exhibit a diamagnetic behavior. The 673 K-calcined Ce(0.97)Fe(0.03)O2 sample is paramagnetic whereas 773 and 873 K-calcined Ce(0.97)Fe(0.03)O2 samples are ferromagnetism having the magnetizations of 4.65 x 10(-3) emu/g and 6.20 x 10(-3) emu/g at 10 kOe, respectively. Our results indicate that the ferromagnetic property is intrinsic to the Fe-doped CeO2 system and is not a result of any secondary magnetic phase or cluster formation.
ABSTRACT
This paper describes the fabrication of barium strontium titanate (Ba0.6Sr0.4TiO3 or BST) nanofibers by electrospinning method using a solution that contained poly(vinylpyrrolidone) and a sol-gel solution of BST. The as-spun and calcined BST/PVP composite nanofibers were characterized by TG-DTA, X-ray diffraction, FT-IR, SEM and TEM, respectively. After calcination of the as-spun BST/PVP composite nanofibers at above 700 degrees C in air for 2 h, BST nanofibers of 188+/-25 nm in diameter having well-developed cubic-perovskite structure were successfully obtained. The crystal structure and morphology of the nanofibers were influenced by the calcination temperature. Calcination at below 700 degrees C resulted in amorphous phase whereas BST with second phase such as barium titanate were formed at above 700 degrees C. Diameters of the nanofibers decreased from 208+/-35 to 161+/-18 nm with increasing calcination temperature between 600 and 800 degrees C.
