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Richard M. Lambert
Researcher at University of Cambridge
Publications - 405
Citations - 17722
Richard M. Lambert is an academic researcher from University of Cambridge. The author has contributed to research in topics: Catalysis & Chemisorption. The author has an hindex of 66, co-authored 405 publications receiving 16854 citations. Previous affiliations of Richard M. Lambert include Spanish National Research Council & University of Seville.
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Selective oxidation with dioxygen by gold nanoparticle catalysts derived from 55-atom clusters
Mark Turner,Vladimir B. Golovko,Vladimir B. Golovko,Owain P. H. Vaughan,Pavel Abdulkin,Ángel Berenguer-Murcia,Mintcho S. Tikhov,Brian F. G. Johnson,Richard M. Lambert +8 more
TL;DR: The observations suggest that catalytic activity arises from the altered electronic structure intrinsic to small gold nanoparticles, and that the use of 55-atom gold clusters may prove a viable route to the synthesis of robust gold catalysts suited to practical application.
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Effective Visible Light-Activated B-Doped and B,N-Codoped TiO2 Photocatalysts
Su-Il In,Alexander Orlov,Regina Berg,Felipe García,Sergio Pedrosa-Jimenez,Mintcho S. Tikhov,Dominic S. Wright,Richard M. Lambert +7 more
TL;DR: A simple low cost method permits controlled, reproducible doping of TiO2 anatase by boron and the resulting materials exhibit red-shifted absorption spectra and unprecedented photocatalytic activity under visible light.
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New insights into the origin of visible light photocatalytic activity of nitrogen-doped and oxygen-deficient anatase TiO2.
TL;DR: These ab initio calculations reveal that the optical absorption of nitrogen-doped TiO2 in the visible light region is primarily located between 400 and 500 nm, while that of oxygen-deficientTiO2 is mainly above 500 nm.
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A single crystal study of the silver-catalysed selective oxidation and total oxidation of ethylene
TL;DR: In this article, the authors investigated the performance of both partial and total oxidization of Ag(111) single crystal surface at pressures of up to 50 Torr, and showed that H-transfer rather than C-C cleavage is rate-determining in the combustion of both ethylene and ethylene oxide.