4 years ago

Catalytically active highly metallic palladium on carbon support for oxidation of HCOO−

Catalytically active highly metallic palladium on carbon support for oxidation of HCOO−
Catalytically active highly metallic palladium (A-I-Pd/C) catalyst for oxidation of formate (HCOO) was synthesized via borohydride reduction method assisted by ammonia and iodine ion. The physico-chemical characterizations were conducted to investigate properties of the synthesized catalysts and we confirmed A-I-Pd/C is consisted with palladium hydride. The catalytic activity of the catalysts for oxidation of HCOO are characterized by electrochemical analysis and A-I-Pd/C catalysts performed the best catalytic activity for oxidation of HCOO in terms of Tafel slope and onset potential. The enhanced catalytic activity of A-I-Pd/C is explained by enhanced kinetics of oxidation of Hads, which is caused by weaken adsorption strength of Hads on Pd due to electron transfer from H to Pd. The enhanced performance of A-I-Pd/C was also confirmed and compared with the others in a single cell system.

Publisher URL: www.sciencedirect.com/science

DOI: S0920586117302559

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.