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Santa Barbara, CA, United States

Cooper R.,University of California at Santa Barbara | Rahinov I.,University of California at Santa Barbara | Rahinov I.,Weizmann Institute of Science | Li Z.,University of California at Santa Barbara | And 3 more authors.
Chemical Science | Year: 2010

Vibrational overtone excitation is, in general, inefficiently stimulated by photons, but can under some circumstances be efficiently stimulated by electrons. Here, we demonstrate electron mediated vibrational overtone excitation in molecular collisions with a metal surface. Specifically, we report absolute vibrational excitation probabilities to v = 1 and 2 for collisions of NO(v = 0) with a Au(111) surface as a function of surface temperature from 300 to 985 K. In all cases, the observed populations of vibrationally excited NO are near those expected for complete thermalization with the surface, despite the fact that the scattering occurs through a direct ''single bounce'' mechanism of sub-ps duration. We present a state-to-state kinetic model, which accurately describes the case of near complete thermalization (a regime we call the strong coupling case) and use this model to extract state-to-state rate constants. This analysis unambiguously shows that direct vibrational overtone excitation dominates the production of v = 2 and that, within the context of our model, the intrinsic strength of the overtone transition is of the same order as the single quantum transition, suggesting a possible way to circumvent optical selection rules in vibrational pumping of molecules. This result also suggests that previous measurements of vibrational relaxation of highly vibrationally excited NO exhibiting highly efficient multi-quantum jumps (δ v~-8) are mechanistically similar to vibrational excitation of NO(v = 0). © The Royal Society of Chemistry 2010. Source


Grant
Agency: National Science Foundation | Branch: | Program: SBIR | Phase: Phase I | Award Amount: 99.97K | Year: 2009

This Small Business Innovation Research Phase I project is an innovative route to produce liquid fuels from biomass. The process will convert biomass, including lignocellulosic biomass, to liquid fuels, with three key steps. First, a synthetic natural gas (SNG) or biogas is generated by either anaerobic digestion or by catalytic hydrothermal gasification. The SNG is rich in methane, which is activated with bromine to produce methyl bromide. Finally, the methyl bromide is coupled catalytically to higher hydrocarbons. Each of the steps is known, but proof of concept has not been established. Feasibility of the technology will be determined through a series of carefully planned laboratory experiments. It is anticipated that this research will exhibit technical viability, and demonstrate commercial feasibility. GRT has substantial experience with and intellectual property related to converting natural gas to fuels; the project is a natural extension of in-house expertise, utilizing existing facilities. Substantial demand for carbon-neutral renewable fuels exists in contemporary society. The project contemplates a process to convert biomass into hydrocarbon fuels, with substantial market impact. The US DOE has estimated that as much as a billion tons per year of biomass is available sustainably for conversion to biofuels, sufficient to displace one third of petroleum use in the US. Society requires a process to produce biofuels at costs competitive with petroleum; a successful outcome to the project will satisfy that demand. GRT has partnered with Fortune 100 companies in the past for process development. Should technical and economic viability of the process be demonstrated, a similar partnership is anticipated. This award is funded under the American Recovery and Reinvestment Act of 2009 (Public Law 111-5).


Trademark
GRT, Inc. | Date: 2016-07-10

Nutraceuticals for use as a dietary supplement.


Trademark
GRT, Inc. | Date: 2012-08-07

A series of books and written articles in the field of health.


Patent
GRT, Inc. | Date: 2012-05-23

A process is disclosed that includes brominating a C

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