Hasniah Aliah, Ryan N. Iman, Sriwidati Sriwidati, Asti Sawitri, Andhy Setiawan, Assa P. D. Putri, Fera Kurniawati
This work aimed to study the natural dye extracted from Indonesian wild plants (Rivina humilis L.) using different solvents. The natural dye was extracted using the maceration method. Three different solvents, namely, aquades, acetone, and ethanol 96%, were used to extract natural dye from Rivina humilis L fruit. The absorbance spectra of the extracted dye were recorded using Ultraviolet-Visible (UV-Vis) spectroscopy. The different spectra of betalain pigment revealed the dye extract’s dependence on the solvent. The functional groups of the extracted dye were analyzed using Fourier transform infrared (FTIR) spectroscopy. The adherence of carbonyl and hydroxyl groups from FTIR spectra indicated that this dye could anchor to a semiconducting material, e.g., TiO2, which was commonly used in dye-sensitized solar cells (DSSC). The electrochemical properties of the extracted pigments were studied through higher occupied molecular orbital (HOMO) and lower unoccupied molecular orbital (LUMO) energy levels. Based on the results, the best performance to construct DSSC was achieved by natural dye adsorption with aquades solvent. © License CC-BY 4.0
Department of Physics, Faculty of Science and Technology, UIN Sunan Gunung Djati Bandung, Jl. A.H Nasution No. 105, Cibiru, 40614, Indonesia; Department of Physics, College of Engineering and Physics, King Fahd University of Petroleum and Minerals, Academic Belt Road, Dhahran, 31261, Saudi Arabia; Study Program of Physics, Faculty of Mathematics and Science, Universitas Halim Sanusi, Jl. Garut No.2, Jawa Barat, Bandung, 40271, Indonesia; Study Program of Physics, Faculty of Science and Mathematics, Universitas Pendidikan Indonesia, Jl. Dr. Setiabudhi No. 229, Bandung, 40154, Indonesia
Research at a Glance
Register to unlockTopics & SDG Alignment
Register to unlockCollaboration
Register to unlockAuthor Profile (Selected)
Register to unlockReferences Overview
Register to unlockJournal & Source
Register to unlockMetadata & Integrity
Register to unlock