Photochemical route for synthesizing atomically dispersed palladium catalysts

Pengxin Liu(Collaborative Innovation Center of Chemistry for Energy Materials), Yun Zhao(Collaborative Innovation Center of Chemistry for Energy Materials), Ruixuan Qin(Collaborative Innovation Center of Chemistry for Energy Materials), Shiguang Mo(Collaborative Innovation Center of Chemistry for Energy Materials), Guangxu Chen(Collaborative Innovation Center of Chemistry for Energy Materials), Lin Gu(Institute of Physics), Daniel M. Chevrier(Dalhousie University), Peng Zhang(Dalhousie University), Qing Guo(Collaborative Innovation Center of Chemistry for Energy Materials), Dandan Zang(Collaborative Innovation Center of Chemistry for Energy Materials), Binghui Wu(Collaborative Innovation Center of Chemistry for Energy Materials), Gang Fu(Collaborative Innovation Center of Chemistry for Energy Materials), Nanfeng Zheng(Collaborative Innovation Center of Chemistry for Energy Materials)
Science
May 12, 2016
Cited by 1,967

Abstract

Atomically dispersed noble metal catalysts often exhibit high catalytic performances, but the metal loading density must be kept low (usually below 0.5%) to avoid the formation of metal nanoparticles through sintering. We report a photochemical strategy to fabricate a stable atomically dispersed palladium-titanium oxide catalyst (Pd1/TiO2) on ethylene glycolate (EG)-stabilized ultrathin TiO2 nanosheets containing Pd up to 1.5%. The Pd1/TiO2 catalyst exhibited high catalytic activity in hydrogenation of C=C bonds, exceeding that of surface Pd atoms on commercial Pd catalysts by a factor of 9. No decay in the activity was observed for 20 cycles. More important, the Pd1/TiO2-EG system could activate H2 in a heterolytic pathway, leading to a catalytic enhancement in hydrogenation of aldehydes by a factor of more than 55.


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