Sanjaya D. Senanayake

Dr. Sanjaya D. Senanayake


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2014 in Science
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Journal Article
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JGJesús Graciani
Jesús Graciani
KMKumudu Mudiyanselage
Kumudu Mudiyanselage
FXFang Xu
Fang Xu
ABAshleigh E. Baber
Ashleigh E. Baber
JEJaime Evans
Jaime Evans
JRJosé A. Rodriguez
José A. Rodriguez
Converting CO 2 into methanol by catalysis: By hydrogenating CO 2 , scientists can transform a greenhouse gas into methanol, a desirable fuel. Graciani et al. cast copper in the role of the highly active catalyst for this reaction by putting copper particles on cerium oxide. The interface between the cerium oxide and the copper enables the reverse water-gas shift reaction that converts CO 2 into CO, which reacts more readily with hydrogen to make methanol. This result takes a step forward in innovating catalysts for this environmentally friendly process. Science , this issue p. 546

24 November 2014 in ACS Applied Materials & Interfaces
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Journal Article
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SBSeong-Min Bak
Seong-Min Bak
Enyuan HuEnyuan Hu
Enyuan Hu
YZYongning Zhou
Yongning Zhou
XYXiqian Yu
Xiqian Yu
SSSanjaya D. Senanayake
Sanjaya D. Senanayake
KNKyung-Wan Nam
Kyung-Wan Nam

7 May 2012 in Journal of the American Chemical Society
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Journal Article
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ABAlbert Bruix
Albert Bruix
JRJosé A. Rodriguez
José A. Rodriguez
PRPedro J. Ramírez
Pedro J. Ramírez
SSSanjaya D. Senanayake
Sanjaya D. Senanayake
JEJaime Evans
Jaime Evans
FIFrancesc Illas
Francesc Illas

30 September 2015 in ACS Catalysis
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Journal Article
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JRJosé A. Rodriguez
José A. Rodriguez
PLPing Liu
Ping Liu
DSDario J. Stacchiola
Dario J. Stacchiola
SSSanjaya D. Senanayake
Sanjaya D. Senanayake
MWMichael G. White
Michael G. White
JCJingguang G. Chen
Jingguang G. Chen

4 May 2016 in Angewandte Chemie International Edition
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ZLZongyuan Liu
Zongyuan Liu
DGDavid C. Grinter
David C. Grinter
PLPablo G. Lustemberg
Pablo G. Lustemberg
TPThuy Duong Nguyen Phan
Thuy Duong Nguyen Phan
YZYinghui Zhou
Yinghui Zhou
JRJosé A. Rodriguez
José A. Rodriguez

17 February 2017 in Chemical Society Reviews
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Journal Article
Closed access
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JRJosé A. Rodriguez
José A. Rodriguez
DGDavid C. Grinter
David C. Grinter
ZLZongyuan Liu
Zongyuan Liu
RPRobert M. Palomino
Robert M. Palomino
SSSanjaya D. Senanayake
Sanjaya D. Senanayake
Model metal/ceria and ceria/metal catalysts have been shown to be excellent systems for studying fundamental phenomena linked to the operation of technical catalysts. In the last fifteen years, many combinations of well-defined systems involving different kinds of metals and ceria have been prepared and characterized using the modern techniques of surface science. So far most of the catalytic studies have been centered on a few reactions: CO oxidation, the hydrogenation of CO2, and the production of hydrogen through the water–gas shift reaction and the reforming of methane or alcohols. Using model catalysts it has been possible to examine in detail correlations between the structural, electronic and catalytic properties of ceria–metal interfaces. In situ techniques (X-ray photoelectron spectroscopy, X-ray absorption spectroscopy, infrared spectroscopy, scanning tunneling microscopy) have been combined to study the morphological changes under reaction conditions and investigate the evolution of active phases involved in the cleavage of C–O, C–H and C–C bonds. Several studies with model ceria catalysts have shown the importance of strong metal–support interactions. In general, a substantial body of knowledge has been acquired and concepts have been developed for a more rational approach to the design of novel technical catalysts containing ceria.