4.6 Article

Bismuth-Induced Integration of Solar Energy Conversion with Synergistic Low-Temperature Catalysis in Ce1-xBixO2-δ Nanorods

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 117, Issue 46, Pages 24242-24249

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp4092943

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Funding

  1. National Basic Research Program of China [2013CB933203, 2010CB933503]
  2. National Natural Science Foundation of China [51272269, 51272303, 51102262]
  3. Science Foundation for Youth Scholar of State Key Laboratory of High Performance Ceramics and Superfine Microstructures [SKL201204]

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For conventional photocatalysis, the energy threshold rather than merely the spectral response is always restricted that the infrared part (48% of solar energy) has never been efficiently utilized, undesirably elevating the temperature and damaging the photon-to-electron conversion. It remains challenging to conquer the IR-related contradiction and integrate the infrared energy into the solar energy conversion. Herein, we logically designed a Bi-induced synergistic photo/thermocatalyst (fluorite Ce(1-x)nanorods), where the coupled ionic conductivity accompanying highly reductive Bi and concomitant oxygen vacancies helped bring about integration of photocatalysis with synergistic low temperature (20-80 C, IR-driven) catalysis, promising for the effective utilization of infrared energy. More generally, through our results a feasible methodology is verified in detail that integration of semiconductor

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