Karim, Kaykobad Md Rezaul and Ong, Huei Ruey and Hamidah, Abdullah and Yousuf, Abu and Cheng, C. K. and Khan, Maksudur R. (2018) Photoelectrochemical reduction of carbon dioxide to methanol on p-type CuFe2O4 under visible light irradiation. International Journal of Hydrogen Energy, 43 (39). pp. 18185-18193. ISSN 0360-3199. (Published)
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Abstract
Artificial photosynthesis has the potential to produce solar fuels from CO2 and H2O using an efficient photocatalyst. Semiconductor with low band gap and high stability is always the right candidate to be used as photocatalyst. Photocatalytic (PC) reduction of CO2 suffers from slow reaction kinetics and poor yield of product. Photocatalytic reaction in assistance with judicious bias potential is a solution to increase the catalytic activity and reduce the electron/hole (e−/h+) recombination rate. In the present work, a p-type CuFe2O4 was synthesized and used for photoelectrochemical (PEC) CO2 reduction. The catalyst was characterized by UV-visible spectroscopy (UV-vis), Mott-Schottky (MS), chronoamperometry, X-Ray powder diffraction (XRD), X-Ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). Methanol was found as only product in liquid phase produced by photoelectrochemical reduction of CO2 at a bias potential of −0.5 V (vs NHE) under light irradiation (at 470 nm). The quantum efficiency and incident photon to current efficiency(IPCE) were found as 14.4% and 5.1% respectively revealed that, CuFe2O4 is a potential photocathode for PEC of CO2 reduction.
Item Type: | Article |
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Additional Information: | Indexed by Scopus |
Uncontrolled Keywords: | CuFe2O4; CO2 reduction; Photoelectrochemical reduction; IPCE; Quantum efficiency |
Subjects: | T Technology > TP Chemical technology |
Faculty/Division: | Centre of Excellence: Centre of Excellence for Advanced Research in Fluid Flow Faculty of Chemical & Natural Resources Engineering |
Depositing User: | Mrs. Neng Sury Sulaiman |
Date Deposited: | 21 Nov 2018 03:36 |
Last Modified: | 21 Nov 2018 03:36 |
URI: | http://umpir.ump.edu.my/id/eprint/22399 |
Download Statistic: | View Download Statistics |
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