1,721,366 research outputs found
Optimized structure and vibrational properties by error affected potential energy surfaces
No full textThe precise theoretical determination of the geometrical parameters of molecules at the minima of their potential energy surface and of the corresponding vibrational properties are of fundamental importance for the interpretation of vibrational spectroscopy experiments. Quantum Monte Carlo techniques are correlated electronic structure methods promising for large molecules, which are intrinsically affected by stochastic errors on both energy and force calculations, making the mentioned calculations more challenging with respect to other more traditional quantum chemistry tools. To circumvent this drawback in the present work, we formulate the general problem of evaluating the molecular equilibrium structures, the harmonic frequencies, and the anharmonic coefficients of an error affected potential energy surface. The proposed approach, based on a multidimensional fitting procedure, is illustrated together with a critical evaluation of systematic and statistical errors. We observe that the use of forces instead of energies in the fitting procedure reduces the statistical uncertainty of the vibrational parameters by 1 order of magnitude. Preliminary results based on variational Monte Carlo calculations on the water molecule demonstrate the possibility to evaluate geometrical parameters and harmonic and anharmonic coefficients at this level of theory with an affordable computational cost and a small stochastic uncertainty (<0.07% for geometries and <0.7% for vibrational properties). © 2012 American Chemical Society
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Small- and Large-Scale Conformational Changes of Adenylate Kinase: A Molecular Dynamics Study of the Subdomain Motion and Mechanics
No full textAbstractAdenylate kinase, an enzyme that catalyzes the phosphoryl transfer between ATP and AMP, can interconvert between the open and catalytically potent (closed) forms even without binding ligands. Several aspects of the enzyme elasticity and internal dynamics are analyzed here by atomistic molecular dynamics simulations covering a total time span of 100ns. This duration is sufficiently long to reveal a partial conversion of the enzyme that proceeds through jumps between structurally different substates. The intra- and intersubstates contributions to the enzyme's structural fluctuations are analyzed and compared both in magnitude and directionality. It is found that, despite the structural heterogeneity of the visited conformers, the generalized directions accounting for conformational fluctuations within and across the substates are mutually consistent and can be described by a limited set of collective modes. The functional-oriented nature of the consensus modes is suggested by their good overlap with the deformation vector bridging the open and closed crystal structures. The consistency of adenylate kinase's internal dynamics over timescales wide enough to capture intra- and intersubstates fluctuations adds elements in favor of the recent proposal that the free (apo) enzyme possesses an innate ability to sustain the open/close conformational changes
Ab initio molecular dynamics with noisy forces: Validating the quantum Monte Carlo approach with benchmark calculations of molecular vibrational properties
Full text linkWe present a systematic study of a recently developed ab initio simulation scheme based on molecular dynamics and quantum Monte Carlo. In this approach, a damped Langevin molecular dynamics is employed by using a statistical evaluation of the forces acting on each atom by means of quantum Monte Carlo. This allows the use of an highly correlated wave function parametrized by several variational parameters and describing quite accurately the Born-Oppenheimer energy surface, as long as these parameters are determined at the minimum energy condition. However, in a statistical method both the minimization method and the evaluation of the atomic forces are affected by the statistical noise. In this work, we study systematically the accuracy and reliability of this scheme by targeting the vibrational frequencies of simple molecules such as the water monomer, hydrogen sulfide, sulfur dioxide, ammonia, and phosphine. We show that all sources of systematic errors can be controlled and reliable frequencies can be obtained with a reasonable computational effort. This work provides convincing evidence that this molecular dynamics scheme can be safely applied also to realistic systems containing several atoms. © 2014 AIP Publishing LLC
Percolation transition in a dynamically clustered network
No full textWe consider a percolationlike phenomenon on a generalization of the Barabási-Albert model, where a modification of the growth dynamics directly allows formation of disconnected clusters. The transition is located with high precision by an original numerical technique based on the comparison of the largest and second largest clusters. A careful investigation focusing on finite size scaling allows us to highlight properties which would hardly be accessible by an analytical solution of cluster growth equations in the stationary limit. Our analysis shows that some critical features of the percolation transition are different from those observed in the case of dilution in fully grown networks. At variance with other models of percolation on growing networks we also find evidence that the order parameter approaches zero as a power of the field p- pc driving the transition, rather than as a stretched exponential. This behavior does not agree with the Berezinskii-Kosterlitz- Thouless scenario found in other similar models. For describing the phase in which a giant cluster develops, a key role is played by the crossover number of nodes Nx ∼ (p- pc) -ζ with ζ 4. This power law behavior and that of other quantities are conjectured on the basis of scaling arguments and numerical evidence. © 2007 The American Physical Society
Ab initio molecular dynamics with noisy forces: Validating the quantum Monte Carlo approach with benchmark calculations of molecular vibrational properties
No full textWe present a systematic study of a recently developed ab initio simulation scheme based on molecular dynamics and quantum Monte Carlo. In this approach, a damped Langevin molecular dynamics is employed by using a statistical evaluation of the forces acting on each atom by means of quantum Monte Carlo. This allows the use of an highly correlated wave function parametrized by several variational parameters and describing quite accurately the Born-Oppenheimer energy surface, as long as these parameters are determined at the minimum energy condition. However, in a statistical method both the minimization method and the evaluation of the atomic forces are affected by the statistical noise. In this work, we study systematically the accuracy and reliability of this scheme by targeting the vibrational frequencies of simple molecules such as the water monomer, hydrogen sulfide, sulfur dioxide, ammonia, and phosphine. We show that all sources of systematic errors can be controlled and reliable frequencies can be obtained with a reasonable computational effort. This work provides convincing evidence that this molecular dynamics scheme can be safely applied also to realistic systems containing several atoms
Percolation transition in a dynamically clustered network
No full textWe consider a percolationlike phenomenon on a generalization of the Barabasi-Albert model, where a modification of the growth dynamics directly allows formation of disconnected clusters. The transition is located with high precision by an original numerical technique based on the comparison of the largest and second largest clusters. A careful investigation focusing on finite size scaling allows us to highlight properties which would hardly be accessible by an analytical solution of cluster growth equations in the stationary limit. Our analysis shows that some critical features of the percolation transition are different from those observed in the case of dilution in fully grown networks. At variance with other models of percolation on growing networks we also find evidence that the order parameter approaches zero as a power of the field p-p(c) driving the transition, rather than as a stretched exponential.This behavior does not agree with the Berezinskii-Kosterlitz-Thouless scenario found in other similar models. For describing the phase in which a giant cluster develops, a key role is played by the crossover number of nodes N-x similar to(p-p(c))(-zeta) with zeta similar or equal to 4. This power law behavior and that of other quantities are conjectured on the basis of scaling arguments and numerical evidence
Finite-temperature electronic simulations without the Born-Oppenheimer constraint
No full textThe adiabatic approximation, typically assumed when performing standard Born-Oppenheimer (BO) molecular dynamics, can become unreliable at finite temperature, and specifically when the temperature is larger than the electronic energy gap between the ground state and the low-lying excited states. In this regime, relevant for many important chemical processes, the non-adiabatic couplings between the electronic energy states can produce finite temperature effects in several molecular properties, such as the geometry, the vibrational frequencies, the binding energy, and several chemical reactions. In this work, we introduce a novel finite-temperature non-adiabatic molecular dynamics based on a novel covariant formulation of the electronic partition function. In this framework, the nuclei are not constrained to move in a specific electronic potential energy surface. Then, by using a rigorous variational upper bound to the free energy, we are led to an approximate partition function that can be evaluated numerically. The method can be applied to any technique capable to provide an energy value over a given wave function ansatz depending on several variational parameters and atomic positions. In this work, we have applied the proposed method within a quantum Monte Carlo (QMC) scheme. In particular, we consider in this first application only classical ions, but we explicitly include an electronic correlation (Jastrow) term in the wave function, by extending in this way the standard variational QMC method, from ground state to finite temperature properties. We show that our approximation reduces correctly to the standard ground-state Born-Oppenheimer (gsBO) at zero temperature and to the correct high temperature limit. Moreover, at temperatures large enough, this method improves the upper bound of the free energy obtained with a single BO energy surface, since within our approach it is possible to estimate the electron entropy of a correlated ansatz in an efficient way. We test this new method on the simple hydrogen molecule, where at low temperature we recover the correct gsBO low temperature limit. Moreover, we show that the dissociation of the molecule is possible at a temperature much smaller than the one corresponding to the gsBO energy surface, in good agreement with experimental evidence. Several extensions of the proposed technique are also discussed, as for instance the inclusion of quantum effects for ions and the calculation of critical (magnetic, superconducting) temperatures. © 2012 American Institute of Physics
Variations on the Author
Full text link“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
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