Journal
SOLAR ENERGY MATERIALS AND SOLAR CELLS
Volume 248, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.solmat.2022.112002
Keywords
ZnO/g-C3N4 binary heterostructure; N3 dye; Dye sensitized solar cell; Blocking layer; Suppression of electron reverse recombination
Funding
- Department of Science and Technology (DST, Nano-Mission Program)
- Council of Scientific and Industrial Research (CSIR), Government of India
- Department of Science and Technology (DST), Government of India
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A simple low-temperature hydrothermal route was used to prepare binary ZnO/g-C3N4 heterostructures, which showed improved performance in DSSC application. The growth of g-C3N4 layer on ZnO nanorods surface delayed electron recombination and increased electron concentration in the photoelectrode.
A simple low-temperature hydrothermal route was adopted to prepare the binary ZnO/g-C3N4 heterostructures, which were thoroughly characterized by various spectroscopic and microscopic probes. The clearly visible interfaces between the ZnO NRs and g-C3N4 in the HRTEM micrograph verify the formation of ZnO/g-C3N4 heterojunction structures, which, combined with N3 dye, deliver increased optical absorption extending from UV to the visible range. The binary ZnO/g-C3N4 heterostructures are used as the photoanode in the DSSC application. Improvement in the DSSC performance arises because of the growth of the g-C3N4 layer on the ZnO nanorods surface, which efficiently delays the reverse recombination of electrons from ZnO to the electrolyte. The g-C3N4 layer also increases the electron concentration in the photoelectrode and, thereby, directly contributes to the improved performance of the DSSC device. The optimal DSSC based on the ZnO/g-v photoanode delivers its characteristic J(SC) similar to 14.18 mA/cm(2), V-OC similar to 544 mV, FF similar to 0.586 and. similar to 4.52%, which is about 2.3 times greater than the DSSC efficiency based on pure ZnO nanorod photoelectrode and retains the spirit of generating the green energy following the photovoltaic endeavor.
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