Driving energetically unfavorable dehydrogenation dynamics with plasmonics

Author:

Sytwu Katherine1ORCID,Vadai Michal2ORCID,Hayee Fariah3,Angell Daniel K.2ORCID,Dai Alan4ORCID,Dixon Jefferson5ORCID,Dionne Jennifer A.2ORCID

Affiliation:

1. Department of Applied Physics, Stanford University, 348 Via Pueblo, Stanford, CA 94305, USA.

2. Department of Materials Science and Engineering, Stanford University, 496 Lomita Mall, Stanford, CA 94305, USA.

3. Department of Electrical Engineering, Stanford University, 350 Jane Stanford Way, Stanford, CA 94305, USA.

4. Department of Chemical Engineering, Stanford University, 443 Via Ortega, Stanford, CA 94305, USA.

5. Department of Mechanical Engineering, Stanford University, 440 Escondido Mall, Stanford, CA 94305, USA.

Abstract

Coaxing unreactive sites Optical excitation of localized surface plasmon resonances can confine light and create electromagnetic (EM) “hotspots” that can increase catalytic reaction rates. Sytwu et al. show how optical excited plasmons can also control the location of the active site. A crossed-bar gold-palladium hydride (Au-PdH x ) plasmonic antenna-reactor system localized EM radiation away from the more reactive PdH x tips. Using in situ environmental transmission electron microscopy, the authors show that changing the illumination wavelength and intensity, along with the surrounding hydrogen gas pressure, could shift dehydrogenation away from the sharp PdH x nanorod tips to the flat middle faces. Science , this issue p. 280

Funder

National Science Foundation

U.S. Department of Energy

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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