The photoelectrocatalytic CO2 reduction on TiO2@ZnO heterojunction by tuning the conduction band potential
The photoelectrocatalytic CO2 reduction is an attracting research field in chemistry, materials, environment and energy science. In this paper, a heterojunction TiO2@ZnO was in-situ fabricated onto the FTO glass. The multi-functionalized heterojunctions of M-TiO2@ZnO/FTO (M = Pd, Pt, Ni and Au) were...
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Published in: | Electrochimica acta Vol. 285; pp. 23 - 29 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier Ltd
20-09-2018
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Subjects: | |
Online Access: | Get full text |
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Summary: | The photoelectrocatalytic CO2 reduction is an attracting research field in chemistry, materials, environment and energy science. In this paper, a heterojunction TiO2@ZnO was in-situ fabricated onto the FTO glass. The multi-functionalized heterojunctions of M-TiO2@ZnO/FTO (M = Pd, Pt, Ni and Au) were used as photocathodes in the photoelectrocatalytic cell of dye/M-TiO2@ZnO/FTO|KHCO3|BiVO4. The working electrodes of dye/M-TiO2@ZnO/FTO were characterized by SEM, TEM, XRD, EPR, UV–vis, and FT-IR spectra. These photoelectrocatalytic cells convert efficiently CO2 to hydrocarbons at voltage of −0.6 ∼ − 1.0 V under simulated sunlight irradiation. The conduction band potential of heterojunction TiO2@ZnO/FTO was adjusted by metal deposition, including Pd, Pt, Ni and Au, which can basically affect the process of CO2 reduction and give different selectivity for hydrocarbons, such as, methanol, ethanol, formic acid and acetic acid. The M-TiO2@ZnO/FTO photocathodes, possessing lower conduction band (CB) than − 0.38 V of standard reduction for methanol, can produce hydrocarbons due to the action of photons. On the other hand, the high electron charge transfer and active Ti3+ cations of TiO2@ZnO/FTO heterojunction could augment the activity of photoelectrocatalytic reduction of carbon dioxide, yielding total hydrocarbons in a formation rate of 62.4 μM cm−2 h−1. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2018.07.216 |