D
Daniel L. DuBois
Researcher at National Renewable Energy Laboratory
Publications - 28
Citations - 4845
Daniel L. DuBois is an academic researcher from National Renewable Energy Laboratory. The author has contributed to research in topics: Hydride & Catalysis. The author has an hindex of 23, co-authored 28 publications receiving 4551 citations. Previous affiliations of Daniel L. DuBois include Pacific Northwest National Laboratory.
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Journal ArticleDOI
Catalysis Research of Relevance to Carbon Management: Progress, Challenges, and Opportunities
Hironori Arakawa,Michele Aresta,John Nelson Armor,Mark A. Barteau,Eric J. Beckman,Alexis T. Bell,John E. Bercaw,Carol Creutz,Eckhard Dinjus,David A. Dixon,Kazunari Domen,Daniel L. DuBois,Juergen Eckert,Etsuko Fujita,Dorothy H. Gibson,William A. Goddard,D. Wayne Goodman,Jay O. Keller,Gregory J. Kubas,Harold H. Kung,James E. Lyons,Leo Ernest Manzer,Tobin J. Marks,Keiji Morokuma,Kenneth M. Nicholas,Roy A. Periana,Lawrence Que,Jens Rostrup-Nielson,Wolfgang M.H. Sachtler,Lanny D. Schmidt,Ayusman Sen,Gabor A. Somorjai,Peter C. Stair,B. Ray Stults,William Tumas +34 more
TL;DR: The goal of the "Opportunities for Catalysis Research in Carbon Management" workshop was to review within the context of greenhouse gas/carbon issues the current state of knowledge, barriers to further scientific and technological progress, and basic scientific research needs in the areas of H2 generation and utilization.
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Development of molecular electrocatalysts for CO2 reduction and H2 production/oxidation.
TL;DR: Progress is described in the development of redox-active carriers capable of concentrating CO(2) and molecular electrocatalysts for CO( 2) reduction, hydrogen production, and hydrogen oxidation, and much more remains to be done.
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Hydrogen oxidation and production using nickel-based molecular catalysts with positioned proton relays
Aaron D. Wilson,Rachel H. Newell,Michael J. McNevin,James T. Muckerman,M. Rakowski DuBois,Daniel L. DuBois +5 more
TL;DR: It is demonstrated that the high catalytic rates observed with these complexes are a result of the positioning of the nitrogen base so that it plays an important role in the formation and cleavage of the H-H bond.
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Gas separations using non-hexafluorophosphate [PF6]− anion supported ionic liquid membranes
TL;DR: In this paper, the authors used room temperature ionic liquids (RTILs) in place of traditional solvents for supported liquid membranes to take advantage of their unique properties, and reported CO 2 permeabilities of 350 barrers (for [Cl] − ) to 1000 barrers(for [Tf 2 N] − ), combined with CO 2 /N 2 ideal selectivities of 15 (for Cl) to 61 (for DCA) − ).
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Measurement of the hydride donor abilities of [HM(diphosphine)2]+ complexes (M = Ni, Pt) by heterolytic activation of hydrogen.
TL;DR: The reactivity of the various [M(diphosphine)2]2+ complexes toward hydrogen parallels their measured hydride acceptor abilities.