4.8 Article

Selective photocatalytic decomposition of formic acid over AuPd nanoparticle-decorated TiO2 nanofibers toward high-yield hydrogen production

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 162, Issue -, Pages 204-209

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apcatb.2014.06.055

Keywords

Photocatalysis; AuPd alloy; Electrospinning; Surface plasmon resonance; Formic acid decomposition

Funding

  1. NTU seed funding for Solar Fuels Laboratory
  2. MOE AcRF-Tier1 [RG 44/11]
  3. MOE AcRF-Tier2 [MOE2012-T2-2-041, ARC 5/13]
  4. CRP program from the Singapore National Research Foundation (NRF) [NRF-CRP5-2009-04]
  5. National Basic Research Program of China (973 Program) [2012CB626801]
  6. National Natural Foundation of China [11274057]
  7. Scientific Research Foundation for Doctor of Liaoning Province [20141118]

Ask authors/readers for more resources

We present high-yield hydrogen production through selective photocatalytic decomposition of formic acid by using electrospun TiO2 nanofibers decorated with AuPd bimetallic alloy nanoparticles under simulated sunlight irradiation. By using only 5 mg of the AuPd/TiO2 nanofibers containing the 0.75% Au and 0.25% Pd, we could achieve an optimal H-2 generation rate of 88.5 mu mol h(-1) with an apparent quantum yield at 365 nm as 15.6%, which is higher than that of the Pd/TiO2 and Au/TiO2 nanofibers by a factor of 1.6 and 4.5, respectively. The enhanced photocatalytic decomposition of formic acid for H-2 generation could be attributed to the stronger electron-sink effect of AuPd alloy nanoparticles, the high selectivity of Pd for the dehydrogenation of formic acid, and the surface plasmon resonance effect of Au. More importantly, we demonstrate that the photocatalytic processes enable re-activation of the AuPd nanoparticles that were poisoned by CO during thermal decomposition of formic acid. As such, the presented AuPd/TiO2 nanofibers are promising materials for re-generation of H-2 under mild conditions from liquid storage carrier of hydrogen. (C) 2014 Elsevier B.V. All rights reserved.

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