scispace - formally typeset
Search or ask a question
Institution

United States Department of Energy

GovernmentWashington D.C., District of Columbia, United States
About: United States Department of Energy is a government organization based out in Washington D.C., District of Columbia, United States. It is known for research contribution in the topics: Coal & Catalysis. The organization has 13656 authors who have published 14177 publications receiving 556962 citations. The organization is also known as: DOE & Department of Energy.
Topics: Coal, Catalysis, Combustion, Oxide, Hydrogen


Papers
More filters
Journal ArticleDOI
TL;DR: A general method for the synthesis of PtZn iNPs on multiwalled carbon nanotubes (MWNT) via a facile and capping agent free strategy using a sacrificial mesoporous silica (mSiO2) shell is reported.
Abstract: Atomically ordered intermetallic nanoparticles (iNPs) have sparked considerable interest in fuel cell applications by virtue of their exceptional electronic and structural properties. However, the synthesis of small iNPs in a controllable manner remains a formidable challenge because of the high temperature generally required in the formation of intermetallic phases. Here we report a general method for the synthesis of PtZn iNPs (3.2 ± 0.4 nm) on multiwalled carbon nanotubes (MWNT) via a facile and capping agent free strategy using a sacrificial mesoporous silica (mSiO2) shell. The as-prepared PtZn iNPs exhibited ca. 10 times higher mass activity in both acidic and basic solution toward the methanol oxidation reaction (MOR) compared to larger PtZn iNPs synthesized on MWNT without the mSiO2 shell. Density functional theory (DFT) calculations predict that PtZn systems go through a “non-CO” pathway for MOR because of the stabilization of the OH* intermediate by Zn atoms, while a pure Pt system forms highly s...

231 citations

Journal ArticleDOI
TL;DR: In this article, the photocatalytic water oxidation activity of hematite (α-Fe2O3) has been greatly enhanced by incorporating hematitic nanoparticles on the reduced graphene oxide (rGO) nanosheets.
Abstract: The photocatalytic water oxidation activity of hematite (α-Fe2O3) has been greatly enhanced by incorporating hematite nanoparticles on the reduced graphene oxide (rGO) nanosheets. Photoelectrochemical measurement results show that coupling the hematite nanoparticles with the rGO greatly increases the photocurrent and reduces the charge recombination rate. Transient absorption spectroscopy and time-domain terahertz spectroscopy have provided the direct evidence that the photogenerated electrons have transferred as the mobile carriers from α-Fe2O3 to rGO, which enhances the charge separation and suppresses the charge recombination. This work has provided new insight into the mechanism of photocatalysis enhancement by reduced graphene oxide, which has implications in the design of semiconductor/graphene heterojunction photocatalysts.

231 citations

Journal ArticleDOI
TL;DR: In this paper, the adsorption and desorption of CO2 on diamine-grafted SBA-15 have been studied by infrared spectroscopy coupled with mass spectrometry.
Abstract: The adsorption and desorption of CO2 on diamine-grafted SBA-15 have been studied by infrared spectroscopy coupled with mass spectrometry. Diamine was grafted onto the SBA-15 surface by the reaction of [N-(2-aminoethyl)-3-aminopropyl]trimethoxysilane with the surface OH. CO2 is adsorbed on the diamine-grafted SBA-15 as bidentate carbonate and bidentate and monodentate bicarbonates at 25 °C. Bidentate carbonate and monodentate bicarbonates are the major surface species formed and decomposed during the concentration-swing adsorption/desorption process at 25 °C. Temperature-programmed desorption revealed that the monodentate and bidentate bicarbonates bound stronger to the diamine-grafted SBA-15 surface than the bidentate carbonate. The amount of CO2 desorbed from the carbonate and bicarbonate between 30 and 120 °C is 2 times more than that of CO2 adsorbed/desorbed during each cycle of the concentration-swing adsorption/desorption. Desorption at 120 °C removes the majority of the captured CO2 and regenerates ...

231 citations

Journal ArticleDOI
TL;DR: The results demonstrate that Pv44CL1, but not Pv4CL2, is the key 4CL isozyme involved in lignin biosynthesis, and reducing lignIn content in switchgrass biomass by silencing Pv4 CL1 can remarkably increase the efficiency of fermentable sugar release for biofuel production.
Abstract: Summary • The lignin content of feedstock has been proposed as one key agronomic trait impacting biofuel production from lignocellulosic biomass. 4-Coumarate:coenzyme A ligase (4CL) is one of the key enzymes involved in the monolignol biosynthethic pathway. • Two homologous 4CL genes, Pv4CL1 and Pv4CL2, were identified in switchgrass (Panicum virgatum) through phylogenetic analysis. Gene expression patterns and enzymatic activity assays suggested that Pv4CL1 is involved in monolignol biosynthesis. Stable transgenic plants were obtained with Pv4CL1 downregulated. • RNA interference of Pv4CL1 reduced extractable 4CL activity by 80%, leading to a reduction in lignin content with decreased guaiacyl unit composition. Altered lignification patterns in the stems of RNAi transgenic plants were observed with phloroglucinol-HCl staining. The transgenic plants also had uncompromised biomass yields. After dilute acid pretreatment, the low lignin transgenic biomass had significantly increased cellulose hydrolysis (saccharification) efficiency. • The results demonstrate that Pv4CL1, but not Pv4CL2, is the key 4CL isozyme involved in lignin biosynthesis, and reducing lignin content in switchgrass biomass by silencing Pv4CL1 can remarkably increase the efficiency of fermentable sugar release for biofuel production.

231 citations

Journal ArticleDOI
TL;DR: In this article, the similarity between photoelectrochemical cells (PECs) and solid state devices is used to model their behavior and optimize such parameters as band gap, doping level, minority carrier lifetime, etc.
Abstract: Photoelectrochemical devices for conversion of solar energy into both electrical energy and chemical energy are discussed with emphasis on how the various material properties of the photoactive electrodes influence device efficiency and stability. The similarity between photoelectrochemical cells (PECs) and solid state devices is used to model their behaviour and optimize such parameters as band gap, doping level, minority carrier lifetime, etc. A model is presented which calculates the electron affinity of any semiconductor and allows the prediction of the open circuit voltage of wet photovoltaic cells and optimum biasing forchemical producing cells. The effects of absorbed ions at the semiconductor/electrolyte interface are reviewed. The temperature dependence of the energy levels in the semiconductor and the electrolyte are considered and the implications of these results to operation of PECs at elevated temperature are discussed. The major differences between PECs and solid state devices are the stability considerations. The thermodynamics of this problem is discussed. Other important degradation mechanisms and some solutions to these problems are reviewed. Finally, a prognosis of the future of this field is presented.

230 citations


Authors

Showing all 13660 results

NameH-indexPapersCitations
Martin White1962038232387
Paul G. Richardson1831533155912
Jie Zhang1784857221720
Krzysztof Matyjaszewski1691431128585
Yang Gao1682047146301
David Eisenberg156697112460
Marvin Johnson1491827119520
Carlos Escobar148118495346
Joshua A. Frieman144609109562
Paul Jackson141137293464
Greg Landsberg1411709109814
J. Conway1401692105213
Pushpalatha C Bhat1391587105044
Julian Borrill139387102906
Cecilia Elena Gerber1381727106984
Network Information
Related Institutions (5)
Lawrence Berkeley National Laboratory
66.5K papers, 4.1M citations

92% related

École Polytechnique Fédérale de Lausanne
98.2K papers, 4.3M citations

90% related

Centre national de la recherche scientifique
382.4K papers, 13.6M citations

89% related

ETH Zurich
122.4K papers, 5.1M citations

88% related

Texas A&M University
164.3K papers, 5.7M citations

88% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20233
202223
2021633
2020601
2019654
2018598