4.6 Article

Enhanced photocatalytic CO2 reduction to CH4 over separated dual co-catalysts Au and RuO2

Journal

NANOTECHNOLOGY
Volume 29, Issue 15, Pages -

Publisher

IOP PUBLISHING LTD
DOI: 10.1088/1361-6528/aaad44

Keywords

co-catalyst; charge separation; photocatalytic; CO2 reduction

Funding

  1. 'Chenguang Program' from Shanghai Education Development Foundation [14CG30]
  2. Shanghai Municipal Education Commission [14CG30]
  3. Shanghai Pujiang Program [17PJD011]
  4. National Natural Science Foundation of China [21773062, 21577036, 5171101651, 21677048]
  5. Science and Technology Commission of Shanghai Municipality [16JC1401400, 17520711500]
  6. State Key Research Development Program of China [2016YFA0204200]

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A spatially separated, dual co-catalyst photocatalytic system was constructed by the stepwise introduction of RuO2 and Au nanoparticles (NPs) at the internal and external surfaces of a three dimensional, hierarchically ordered TiO2-SiO2 (HTSO) framework (the final photocatalyst was denoted as Au/HRTSO). Characterization by HR-TEM, EDS-mapping, XRD and XPS confirmed the existence and spatially separated locations of Au and RuO2. In CO2 photocatalytic reduction (CO2PR), Au/HRTSO (0.8%) shows the optimal performance in both the activity and selectivity towards CH4; the CH4 yield is almost twice that of the singular Au/HTSO or HRTSO (0.8%, weight percentage of RuO2) counterparts. Generally, Au NPs at the external surface act as electron trapping agents and RuO2 NPs at the inner surface act as hole collectors. This advanced spatial configuration could promote charge separation and transfer efficiency, leading to enhanced CO2PR performance in both the yield and selectivity toward CH4 under simulated solar light irradiation.

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