| Literature DB >> 27144344 |
Zongyuan Liu1, David C Grinter2, Pablo G Lustemberg3, Thuy-Duong Nguyen-Phan2, Yinghui Zhou4, Si Luo1, Iradwikanari Waluyo2, Ethan J Crumlin5, Dario J Stacchiola2, Jing Zhou4, Javier Carrasco6, H Fabio Busnengo3, M Verónica Ganduglia-Pirovano7, Sanjaya D Senanayake8, José A Rodriguez9,10.
Abstract
Ni-CeO2 is a highly efficient, stable and non-expensive catalyst for methane dry reforming at relative low temperatures (700 K). The active phase of the catalyst consists of small nanoparticles of nickel dispersed on partially reduced ceria. Experiments of ambient pressure XPS indicate that methane dissociates on Ni/CeO2 at temperatures as low as 300 K, generating CHx and COx species on the surface of the catalyst. Strong metal-support interactions activate Ni for the dissociation of methane. The results of density-functional calculations show a drop in the effective barrier for methane activation from 0.9 eV on Ni(111) to only 0.15 eV on Ni/CeO2-x (111). At 700 K, under methane dry reforming conditions, no signals for adsorbed CHx or C species are detected in the C 1s XPS region. The reforming of methane proceeds in a clean and efficient way.Entities:
Keywords: X-ray photoelectron spectroscopy; ceria; density functional theory; methane dissociation; nickel
Year: 2016 PMID: 27144344 DOI: 10.1002/anie.201602489
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336