Do you want to publish a course? Click here

Exploration of free energy surface and thermal effects on relative population and infrared spectrum of the Be$_6$B$_{11}^{-}$ fluxional cluster

478   0   0.0 ( 0 )
 Added by Jose Luis Cabellos
 Publication date 2021
  fields Physics
and research's language is English




Ask ChatGPT about the research

The starting point to understanding cluster properties is the putative global minimum and all the nearby local energy minima; however, locating them is computationally expensive and challenging due to a combinatorial explosion problem. The relative populations and spectroscopic properties of a molecule that are a function of temperature can be approximately computed by employing statistical thermodynamics. Here, we investigate temperature-entropy-driven isomers distribution on Be$_6$B$_{11}^{-}$ fluxional cluster and the effect of temperature on their infrared spectroscopy and relative populations. We identify the vibration modes possessed by the cluster that significantly contribute to the zero-point energy. A couple of steps are considered for computing the temperature-dependent relative population: First, using a genetic algorithm coupled to density functional theory, we performed an extensive and systematic exploration of the potential/free energy surface of Be$_6$B$_{11}^{-}$ cluster to locate the putative global minimum and elucidate the low-energy structures. Second, the relative populations temperature effects are determined by considering the thermodynamic properties and Boltzmann factors. The temperature-dependent relative populations show that the entropies and temperature are essential for determining the global minimum. We compute the temperature-dependent total infrared spectra employing the Boltzmann factor weighted sums of each isomers infrared spectrum and find that at finite temperature, the total infrared spectrum is composed of an admixture of infrared spectra that corresponds to the spectrum of the lowest energy structure and its isomers located at higher energies. The methodology and results describe the thermal effects in the relative population and the infrared spectra.



rate research

Read More

This study reports the lowest energy structure of bare Cu$_{13}$ nanoclusters as a pair of enantiomers for temperatures ranging from 20 to 1200 K. Moreover, we compute the enantiomerization energy for the interconversion from $mathcal{M}$ to $mathcal{P}$ structures in the chiral putative global minimum for temperatures ranging from 20 to 1300 K. Additionally, employing statistical thermodynamics and nanothermodynamics, we compute the Boltzmann Probability for each particular isomer as a function of temperature. To achieve that, we explore the free energy surface of the Cu$_{13}$ cluster, employing a genetic algorithm coupled with density functional theory and statistical thermodynamics. Moreover, we discuss the energetic ordering of structures computed at the DFT level and compared to high level DLPNO-CCSD(T1) reference energies, and we present chemical bonding analysis using the AdNDP method in the chiral putative global minimum. Based on the computed relative abundances, our results show that the chiral putative global minimum strongly dominates for temperatures ranging from 20 to 1100 K.
The lowest-energy structure, distribution of isomers, and their molecular properties depend significantly on the geometry and temperature. The total energy computations under DFT methodology are typically carried out at zero temperature; thereby, entropic contributions to total energy are neglected, even though functional materials work at finite temperature. In the present study, the probability of occurrence of one particular Be$_4$B$_8$ isomer at temperature T is estimated within the framework of quantum statistical mechanics and nanothermodynamics. To locate a list of all possible low-energy chiral and achiral structures, an exhaustive and efficient exploration of the potential/free energy surface is done by employing a multilevel multistep global genetic algorithm search coupled to DFT. Moreover, we discuss the energetic ordering of structures computed at the DFT level against single-point energy calculations at the CCSD(T) level of theory. The computed VCD/IR spectrum of each isomer is multiplied by their corresponding Boltzmann weight at temperature T; then, they are summed together to produce a final Boltzmann weighted spectrum. Additionally, we present chemical bonding analysis using the Adaptive Natural Density Partitioning method in the chiral putative global minimum. The transition state structures and the enantiomer-enantiomer and enantiomer-achiral activation energies as a function of temperature, evidence that a change from an endergonic to an exergonic type of reaction occurs at a temperature of 739 K.
We report first-principles calculations of acoustic surface plasmons on the (0001) surface of Be, as obtained in the random-phase approximation of many-body theory. The energy dispersion of these collective excitations has been obtained along two symmetry directions. Our results show a considerable anisotropy of acoustic surface plasmons, and underline the capability of experimental measurements of these plasmons to {it map} the electron-hole excitation spectrum of the quasi two-dimensional Shockley surface state band that is present on the Be(0001) surface.
94 - V. G. Artemov , E. Uykur , S. Roh 2019
The most common species in liquid water, next to neutral H$_2$O molecules, are the H$_3$O$^+$ and OH$^-$ ions. In a dynamic picture, their exact concentrations depend on the time scale at which these are probed. Here, using a spectral-weight analysis, we experimentally resolve the fingerprints of the elusive fluctuations-born short-living H$_3$O$^+$, DH$_2$O$^+$, HD$_2$O$^+$, and D$_3$O$^+$ ions in the IR spectra of light (H$_2$O), heavy (D$_2$O), and semi-heavy (HDO) water. We find that short-living ions, with concentrations reaching $sim 2%$ of the content of water molecules, coexist with long-living pH-active ions on the picosecond timescale, thus making liquid water an effective ionic liquid in femtochemistry.
The CO_{2} electro-reduction reaction (CORR) is a promising avenue to convert greenhouse gases into high-value fuels and chemicals, in addition to being an attractive method for storing intermittent renewable energy. Although polycrystalline Cu surfaces have long known to be unique in their capabilities of catalyzing the conversion of CO_{2} to higher-order C1 and C2 fuels, such as hydrocarbons (CH_{4}, C_{2}H_{4} etc.) and alcohols (CH_{3}OH, C_{2}H_{5}OH), product selectivity remains a challenge. In this study, we select three metal catalysts (Pt, Au, Cu) and apply in situ surface enhanced infrared absorption spectroscopy (SEIRAS) and ambient-pressure X-ray photoelectron spectroscopy (APXPS), coupled to density-functional theory (DFT) calculations, to get insight into the reaction pathway for the CORR. We present a comprehensive reaction mechanism for the CORR, and show that the preferential reaction pathway can be rationalized in terms of metal-carbon (M-C) and metal-oxygen (M-O) affinity. We show that the final products are determined by the configuration of the initial intermediates, C-bound and O-bound, which can be obtained from CO_{2} and (H)CO_{3}, respectively. C1 hydrocarbons are produced via OCH_{3, ad} intermediates obtained from O-bound CO_{3, ad} and require a catalyst with relatively high affinity for O-bound intermediates. Additionally, C2 hydrocarbon formation is suggested to result from the C-C coupling between C-bound CO_{ad} and (H)CO_{ad}, which requires an optimal affinity for the C-bound species, so that (H)CO_{ad} can be further reduced without poisoning the catalyst surface. Our findings pave the way towards a design strategy for CORR catalysts with improved selectivity, based on this experimental/theoretical reaction mechanisms that have been identified.
comments
Fetching comments Fetching comments
Sign in to be able to follow your search criteria
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا