| Literature DB >> 27712051 |
Satyapaul A Singh1, Karan Vishwanath1, Giridhar Madras1.
Abstract
Removal of excess amount of hydrogen in a catalytic route is a safety measure to be implemented in fuel cell technologies and in nuclear power plants. Hydrogen and oxygen activation are crucial steps for hydrogen combustion that can be achieved by modifying supports with suitable noble metals. In the present study, Pt- and Pd-substituted Co3O4-ZrO2 (CZ) were synthesized using PEG-assisted sonochemical synthesis. Ionic states of Pt and Pd in CZ supports were analyzed by X-ray photoelectron spectroscopy. Pd and Pt improved H2 and O2 activation extensively, which reduced the temperature of 50% conversion (T50%) to 33 °C compared with the support (CZ). The activation energy of PdCZ catalyst was decreased by more than 2 folds (13.4 ± 1.2 kJ mol-1) compared with CZ (34.3 ± 2.3 kJ mol-1). The effect of oxygen vacancies in the reaction mechanism is found to be insignificant with Pt- and Pd-substituted CZ supports. However, oxygen vacancies play an important role when CZ alone was used as catalyst. The importance of hydrogen and oxygen activation as well as the oxygen vacancies in mechanism was studied by H2-TPD, H2-TPR, and in situ FTIR spectroscopy.Entities:
Keywords: Co3O4; H2 combustion; ZrO2; in situ FTIR; ionic substitution; oxygen storage capacity; temperature programming reduction; temperature-programmed desorption
Year: 2016 PMID: 27712051 DOI: 10.1021/acsami.6b08019
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229