Electro-catalysis of carbon black or titanium sub-oxide supported Pd–Gd towards formic acid electro-oxidation. Issue 73 (20th July 2016)

• Record Type: Journal Article
• Authors: He, Nan; Qin, Chuanguang; Wang, Rumin; Ma, Shuhui; Wang, Yi; Qi, Tao
• Is Part Of: RSC advances. Volume 6:Issue 73(2016)
• Page Start: 68989
• Page End: 68996
• Publication Date: 2016-07-20
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra13097f
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Carbon black supported Pd–Gd catalysts (Pd– x Gd/C, x is weight percent in catalyst) with different amounts of Gd were prepared by a simultaneous reduction reaction with sodium borohydride in aqueous solution. Abstract : Carbon black supported Pd–Gd catalysts (Pd– x Gd/C, x is weight percent in catalyst) with different amounts of Gd were prepared by a simultaneous reduction reaction with sodium borohydride in aqueous solution. The structure, morphology and element valence state of these catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS), respectively. The electro-catalytic performance of these catalysts for formic acid oxidation was investigated using cyclic voltammetry (CV), chronoamperometry (CA) and CO stripping experiments. It is found that the Pd–2.5Gd/C catalyst has a better electro-catalytic activity than the Pd/C catalyst, which can be explained by a bi-functional mechanism. In addition, the higher content of metallic Pd caused by the addition of Gd also contributes to the better catalytic activity of Pd–2.5Gd/C. Based on the good electro-catalytic performance of the Pd–2.5Gd/C, Pd– x Gd/Ti4 O7 ( x stands for weight percentage in whole catalyst) catalysts were also prepared and characterized in the same way. The Pd–2.5Gd/Ti4 O7 and Pd–4Gd/Ti4 O7 catalysts exhibited better catalytic activities than the Pd–2.5Gd/C catalyst, which mainly results from the further increase of metallic Pd caused by Ti4 O7 .