2013
DOI: 10.1016/j.rser.2013.05.027
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Recycling of carbon dioxide to renewable fuels by photocatalysis: Prospects and challenges

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Cited by 162 publications
(83 citation statements)
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“…To better understand the complex processes apparent in the TA spectra, we used a multiexponential decay function to model the different charge carrier relaxation dynamics in the material. Each data set, collected with a single pump wavelength, incident pump fluence, and a series of probe wavelengths (λ), was fit to a sum of exponentials ΔAðλ, tÞ = A 0 ðλ, t ≥ 0Þ + f ðtÞ p X 4 n=1 A n ðλÞe −t=τnðλÞ , [1] where A n and τ n are the amplitudes and time constants for the exponential decays, respectively, A 0 is a constant term (for signal not decaying over the maximum time scale measured by the experiment, which is 2-3 ns), f is the instrument-response function (a Gaussian of width 240 fs, empirically measured using blanks), and the "*" operator represents convolution (27). We did not constrain the fitting to a specific number of decay processes, but rather let it vary as needed to obtain the best fit of the data, using up to a maximum of four exponential terms.…”
Section: Resultsmentioning
confidence: 99%
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“…To better understand the complex processes apparent in the TA spectra, we used a multiexponential decay function to model the different charge carrier relaxation dynamics in the material. Each data set, collected with a single pump wavelength, incident pump fluence, and a series of probe wavelengths (λ), was fit to a sum of exponentials ΔAðλ, tÞ = A 0 ðλ, t ≥ 0Þ + f ðtÞ p X 4 n=1 A n ðλÞe −t=τnðλÞ , [1] where A n and τ n are the amplitudes and time constants for the exponential decays, respectively, A 0 is a constant term (for signal not decaying over the maximum time scale measured by the experiment, which is 2-3 ns), f is the instrument-response function (a Gaussian of width 240 fs, empirically measured using blanks), and the "*" operator represents convolution (27). We did not constrain the fitting to a specific number of decay processes, but rather let it vary as needed to obtain the best fit of the data, using up to a maximum of four exponential terms.…”
Section: Resultsmentioning
confidence: 99%
“…The samples have multiple decay pathways extending over multiple time scales, including those which have time constants much longer than can be measured with a translation stage for pump-probe delay. Therefore, we have divided the discussion into the fraction of the signal whose decay can be followed (amplitudes and time constants A 1-4 and τ [1][2][3][4] , respectively) and the longer-lived fraction (A 0 ). For the picosecond-nanosecond decays, we define the amplitude-weighted average time constant hτðλÞi = P 4 n=1 A n ðλÞτ n ðλÞ P 4 n=1 A n ðλÞ .…”
Section: Resultsmentioning
confidence: 99%
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“…Recently it was shown that this type of Au cluster sufficiently catalysis certain reaction; for example it can activate the CO in CO oxidation [94,95]. We suggest that the molecular-like Au cluster may facilitate the activation of methane for transformation to dehydrogenation (13) and the coupling of methyl to ethane (16) which dominates on Au/TNT as can be seen in Table 2. It is generally accepted that the coupling of methyl radicals favored on gold [96]:…”
Section: Presumed Photocatalytic Mechanism For Au Catalystsmentioning
confidence: 79%
“…The increased emission rate of these gases, especially of CO 2 , contributes to global warming [13]. The dry reforming of CH 4 with CO 2 results in valuable syngas; this would solve the problem if atmospheric or byproduct CO 2 could be used in the reaction [14][15][16][17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%