arXiv subjects

Jonathan J. Dorando

Publications and source records attributed to Jonathan J. Dorando.

5 recordsLinked to original sources

arXiv2009

Perfect Reflection of Chiral Fermions in Gated Graphene Nanoribbons

We describe the results of a theoretical study of transport through gated metallic graphene nanoribbons using a non-equilibrium Green function method. Although analogies with quantum field theory predict perfect transmission of chiral fermions through gated regions in one dimension, we find \emph{perfect reflection} of chiral fermions in armchair ribbons for specific configurations of the gate. This effect should be measurable in narrow graphene constrictions gated by a charged carbon nanotube.

cond-mat.mes-hall↗

arXiv2009

Analytic response theory for the density matrix renormalization group

We propose an analytic response theory for the density matrix renormalization group whereby response properties correspond to analytic derivatives of density matrix renormalization group observables with respect to the applied perturbations. Both static and frequency-dependent response theories are formulated and implemented. We evaluate our pilot implementation by calculating static and frequency dependent polarizabilities of short oligo-di-acetylenes. The analytic response theory is competitive with dynamical density matrix renormalization group methods and yields significantly improved accuracies when using a small number of density matrix renormalization group states. Strengths and weaknesses of the analytic approach are discussed.

cond-mat.str-el↗

arXiv2007

An Introduction to the Density Matrix Renormalization Group Ansatz in Quantum Chemistry

The Density Matrix Renormalisation Group (DMRG) is an electronic structure method that has recently been applied to ab-initio quantum chemistry. Even at this early stage, it has enabled the solution of many problems that would previously have been intractable with any other method, in particular, multireference problems with very large active spaces. Historically, the DMRG was not originally formulated from a wavefunction perspective, but rather in a Renormalisation Group (RG) language. However, it is now realised that a wavefunction view of the DMRG provides a more convenient, and in some cases more powerful, paradigm. Here we provide an expository introduction to the DMRG ansatz in the context of quantum chemistry.

cond-mat.str-el↗

arXiv2007

Targeted Excited State Algorithms

To overcome the limitations of the traditional state-averaging approaches in excited state calculations, where one solves for and represents all states between the ground state and excited state of interest, we have investigated a number of new excited state algorithms. Building on the work of van der Vorst and Sleijpen (SIAM J. Matrix Anal. Appl., 17, 401 (1996)), we have implemented Harmonic Davidson and State-Averaged Harmonic Davidson algorithms within the context of the Density Matrix Renormalization Group (DMRG). We have assessed their accuracy and stability of convergence in complete active space DMRG calculations on the low-lying excited states in the acenes ranging from naphthalene to pentacene. We find that both algorithms offer increased accuracy over the traditional State-Averaged Davidson approach, and in particular, the State-Averaged Harmonic Davidson algorithm offers an optimal combination of accuracy and stability in convergence.

cond-mat.str-el↗

arXiv2007

The radical character of the acenes: A density matrix renormalization group study

We present a detailed investigation of the acene series using high-level wavefunction theory. Our ab-initio Density Matrix Renormalization Group algorithm has enabled us to carry out Complete Active Space calculations on the acenes from napthalene to dodecacene correlating the full pi-valence space. While we find that the ground-state is a singlet for all chain-lengths, examination of several measures of radical character, including the natural orbitals, effective number of unpaired electrons, and various correlation functions, suggests that the longer acene ground-states are polyradical in nature.

cond-mat.str-el↗