期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 115, 期 45, 页码 22587-22597出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp204856c
关键词
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资金
- National Science Council of Taiwan [98-2221-E-006-110-MY3, 99-2622-E-006-010-CC2, 100-3113-E-006-001, 100-3113-E-006-012, 100-3113-E-007-008, 98-2221-E-006-112-MY2]
- Bureau of Energy, Ministry of Economic Affairs, Taiwan [100-D0204-2]
Graphite oxide (GO) photocatalysts derived from graphite oxidation can have varied electronic properties by varying the oxidation level. Absorption spectroscopy shows the increasing band gap of GO with the oxygen content. Electrochemical analysis along with the Mott-Schottky equation show that the conduction and valence band edge levels of GO from appropriate oxidation are suitable for both the reduction and the oxidation of water. The conduction band edge shows little variation with the oxidation level, and the valence band edge governs the bandgap width of GO. The photocatalytic activity of GO specimens with various oxygenated levels was measured in methanol and AgNO3 solutions for evolution of H-2 and O-2, respectively. The H-2 evolution was strong and stable over time, whereas the O-2 evolution was negligibly small due to mutual photocatalytic reduction of the GO with upward shift of the valence band edge under illumination. The conduction band edge of GO showed a negligible change with the illumination. When NaIO3 was used as a sacrificial reagent to suppress the mutual reduction mechanism under illumination, strong O-2 evolution was observed over the GO specimens. The present study demonstrates that chemical modification can easily modify the electronic properties of GO for specific photosynthetic applications.
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