4.6 Article

CO2 capture, storage, and conversion using a praseodymium-modified Ga2O3 photocatalyst

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 5, Issue 36, Pages 19351-19357

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ta04918h

Keywords

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Funding

  1. Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan [2406]
  2. Precursory Research for Embryonic Science and Technology (PRESTO)
  3. Japan Science and Technology Agency (JST)
  4. Program for Elements Strategy Initiative for Catalysts & Batteries (ESICB)
  5. China Scholarship Council
  6. Grants-in-Aid for Scientific Research [15H04187] Funding Source: KAKEN

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Praseodymium-modified gallium oxide (Pr/Ga2O3) was found to show enhanced activity and selectivity toward CO evolution in the photocatalytic conversion of CO2 using H2O as an electron donor in an aqueous solution of NaHCO3 as compared to those of bare Ga2O3. The as-prepared Pr species, including Pr(OH)(3) and Pr2O2CO3, on the surface of Ga2O3 were transformed into Pr hydroxycarbonates (Pr-2(OH)(2(3-x))(CO3)(x)) and Pr carbonate hydrates (Pr-2(CO3)(3)center dot 8H(2)O) in an aqueous solution of NaHCO3, and then the Pr-2(OH)(2(3-x))(CO3)(x) was further transformed into Pr-2(CO3)(3)center dot 8H(2)O by CO2 bubbling under photoirradiation. This indicates that CO2 molecules dissolved in water can be captured and stored using Pr species in an aqueous solution of NaHCO3 under CO2 bubbling. More importantly, Pr-2(OH)(2(3-x))(CO3)(x) and Pr-2(CO3)(3)center dot 8H(2)O accumulated on the surface were decomposed to CO over the Ga2O3 photocatalyst with a Ag cocatalyst. Consequently, Ag/Pr/Ga2O3 exhibits much higher activity (249 mu mol h(-1) of CO) than the pristine Ag-loaded Ga2O3 (136 mu mol h(-1) of CO).

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