Design of Fe-MOF-bpdc deposited with cobalt oxide (CoOx) nanoparticles for enhanced visible-light-promoted water oxidation reaction

This work spotlights the facile method to deposit cobalt oxide (CoO x ) nanoparticles as a cocatalyst on Fe-MOF-bpdc to enhance its photocatalytic activity for water oxidation reaction (WOR) under visible light irradiation to evolve gaseous O 2 . Due to the soft conditions needed for the process dev...

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Veröffentlicht in:Research on chemical intermediates 2020-03, Vol.46 (3), p.2003-2015
Hauptverfasser: Mine, Shinya, Lionet, Zakary, Shigemitsu, Haruka, Toyao, Takashi, Kim, Tae-Ho, Horiuchi, Yu, Lee, Soo Wohn, Matsuoka, Masaya
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Sprache:eng
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Zusammenfassung:This work spotlights the facile method to deposit cobalt oxide (CoO x ) nanoparticles as a cocatalyst on Fe-MOF-bpdc to enhance its photocatalytic activity for water oxidation reaction (WOR) under visible light irradiation to evolve gaseous O 2 . Due to the soft conditions needed for the process developed, the framework structure of Fe-MOF-bpdc was maintained even after the deposition of CoO x . The optimized CoO x @Fe-MOF-bpdc composite showed enhanced activity towards visible-light-driven WOR as compared to pristine Fe-MOF-bpdc, the amount of evolved O 2 being increased by about 2 times at the maximum with CoO x loading of 2 wt% as Co metal. Investigations on the wavelength dependence of visible-light-driven WOR on CoO x @Fe-MOF-bpdc revealed that the direct photo-excitation of Fe-oxo clusters within Fe-MOF-bpdc plays an important role to initiate the reaction. Furthermore, it was found that the rate of 2-propanol oxidation reaction, which is a typical two-electron oxidation reaction, was hardly affected by CoO x deposition, suggesting that CoO x acts as a unique hole trapping site and more preferentially catalyse the four-electron oxidation reactions like WOR than the two-electron oxidation reaction.
ISSN:0922-6168
1568-5675
DOI:10.1007/s11164-019-04077-8