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The development of multifunctional catalysts to replace Pt for fuel oxidation reactions in low temperature fuel cells toward environmentally friendly energy production

Grant number: 13/50206-4
Support type:Program for Research on Bioenergy (BIOEN) - Regular Program Grants
Duration: October 01, 2013 - December 31, 2016
Field of knowledge:Physical Sciences and Mathematics - Chemistry
Cooperation agreement: IUPAC
Principal Investigator:Hebe de las Mercedes Villullas
Grantee:Hebe de las Mercedes Villullas
Principal investigator abroad: Rongrong Chen
Institution abroad: Indiana University, United States
Principal investigator abroad: Shi-Gang Sun
Institution abroad: Xiamen University (XMU), China
Home Institution: Instituto de Química (IQ). Universidade Estadual Paulista (UNESP). Campus de Araraquara. Araraquara , SP, Brazil

Abstract

The environmentally friendly generation of energy has brought new scientific and technological challenges. Among the various alternative systems for energy production, fuel cells are particularly attractive because they allow clean and efficient conversion of chemical energy into electricity. Currently, the most active catalyst for the oxidation of fuels such as hydrogen, methanol and ethanol in fuel cells are Pt and Pt-based materiais, which are too expensive for affordable clean energy production. The development of catalysts based on cheaper materiais for fuel oxidation reactions in fuel cells is needed. The proposal aims to develop novel multi-functional catalysts to replace Pt for fuel oxidation reactions in fuel cells through collaborative efforts by electrochemists from Brazil, USA and China. Specifically, combining electrochemical measurements, in-situ spectroscopy characterizations, density functional theory simulations and fuel cell testing, the joint team will focus on studying reaction mechanisms of hydrogen, methanol and ethanol oxidation reactions (HORs, MORs and EORs) on various catalysts in both acid and alkaline media. Through understanding how surface and electronic structures of various catalysts affect the reaction kinetics of HORs, MORs and EORs in acid verse alkaline media, new multi-functional catalysts based on low cost materiais (such as Pd, Ni and other earth abundant elements) with comparable HORs, MORs and EORs activity to Pt-based catalysts will be designed and characterized. For example, alloying Pd with transition metais will induce structural changes that alter the electronic characteristics of Pd surface active sites and the availability of oxygenated species on the catalyst surface needed to oxidize alcohol and its fragments. The effects of electronic properties on reactivity will also be investigated by varying metal-support interactions. The successful execution of the proposed project will provi de viable new non-precious metal catalysts for fuel oxidation in fuel cells and a means to produce energy in an environmentally friendly fashion. (AU)

Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
GUO, JUNSONG; CHEN, RONGRONG; ZHU, FU-HUN; SUN, SHI-GANG; VILLULLAS, HEBE M. New understandings of ethanol oxidation reaction mechanism on Pd/C and Pd2Ru/C catalysts in alkaline direct ethanol fuel cells. APPLIED CATALYSIS B-ENVIRONMENTAL, v. 224, p. 602-611, MAY 2018. Web of Science Citations: 36.
ALVARENGA, GABRIEL M.; COUTINHO GALLO, IRA B.; VILLULLAS, HEBE M. Enhancement of ethanol oxidation on Pd nanoparticles supported on carbon-antimony tin oxide hybrids unveils the relevance of electronic effects. JOURNAL OF CATALYSIS, v. 348, p. 1-8, APR 2017. Web of Science Citations: 20.
GODOI, DENIS R. M.; VILLULLAS, HEBE M.; ZHU, FU-CHUN; JIANG, YAN-XIA; SUN, SHI-GANG; GUO, JUNSONG; SUN, LILI; CHEN, RONGRONG. A comparative investigation of metal-support interactions on the catalytic activity of Pt nanoparticles for ethanol oxidation in alkaline medium. Journal of Power Sources, v. 311, p. 81-90, APR 15 2016. Web of Science Citations: 23.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.