Citation:
ZHOU Liang, ZHANG Xue-Hua, LIN Lin, LI Pan, SHAO Kun-Juan, LI Chun-Zhong, HE Tao. Visible-Light Photocatalytic Reduction of CO2 by CoTe Prepared via a Template-Free Hydrothermal Method[J]. Acta Physico-Chimica Sinica,
;2017, 33(9): 1884-1890.
doi:
10.3866/PKU.WHXB201705084
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A CoTenanocatalyst has been successfully synthesized via a template-free hydrothermal method. Inorganic reactants were used so as not to introduce carbon residue contamination. The as-prepared sample was characterized by many techniques, including X-ray diffraction, scanning electron microscopy, ultraviolet-visible light absorption spectroscopy, and X-ray photoelectron spectroscopy. The obtained sample was found to be sponge-like CoTe with a hexagonal structure, which exhibited visible-light (λ> 420 nm) photocatalytic activity. Photoreduction of CO2 over CoTe is believed to have undergone via the carbene pathway. The CO2 was photocatalytically reduced into CH4 with a low yield when N,N-dimethylacetamide (DMA) or water was used as the solvent. When the sacrificial agent triethanolamine (TEOA) was introduced into the photocatalytic system, however, the product was CO instead. These results indicated that both the solvent and sacrificial agent can influence the photoreduction of CO2 over the CoTenanocatalyst. Usually, the solubility of CO2 in an organic solvent such as DMA is higher than that in the pure water, leading to a larger product yield. The presence of TEOA may change the adsorption characteristics of CO onto the surface of the CoTe catalyst, as well as enhance the separation efficiency of photogenerated charge carriers, resulting in a change in the activity and selectivity of CO2 photoreduction.
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Keywords:
- CoTe,
- CO2,
- Photocatalytic reduction,
- Organic solvent,
- Sacrificial agent
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