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Artur F. Izmaylov

Researcher at University of Toronto

Publications -  176
Citations -  12341

Artur F. Izmaylov is an academic researcher from University of Toronto. The author has contributed to research in topics: Neutrino & Hamiltonian (quantum mechanics). The author has an hindex of 40, co-authored 162 publications receiving 9487 citations. Previous affiliations of Artur F. Izmaylov include Pierre-and-Marie-Curie University & Rice University.

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Measurement of the neutrino-oxygen neutral-current interaction cross section by observing nuclear deexcitation γ rays

K. Abe, +372 more
- 31 Oct 2014 - 
TL;DR: In this article, the neutrino-oxygen neutral-current quasielastic (NCQE) cross section was measured using the Super-Kamiokande water Cherenkov detector.
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Search for light sterile neutrinos with the T2K far detector Super-Kamiokande at a baseline of 295 km

K. Abe, +320 more
- 30 Apr 2019 - 
TL;DR: In this article, the authors acknowledge the support of MEXT, Japan, NRC and NRC NRC grant No. 713673 and H2020 Grant No. RISE-GA644294.
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Topologically Correct Quantum Nonadiabatic Formalism for On-the-Fly Dynamics.

TL;DR: In this paper, the authors analyze two approaches for nonadiabatic dynamics using the time-dependent variational principle and the adiabatic representation, and show that unless a gauge transformation is used to enforce single-valued boundary conditions, the first approach fails to capture the geometric phase.
Posted Content

Cartan sub-algebra approach to efficient measurements of quantum observables

TL;DR: In this article, a unified Lie algebraic framework is proposed for measuring expectation values of Hamiltonians appearing in the Variational Quantum Eigensolver approach to quantum chemistry, which is based on embedding the observable operator in a Lie algebra and transforming Lie algebra elements into those of a Cartan sub-algebra (CSA) using unitary operators.
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Multipartitioning many-body perturbation theory calculations on temporary anions: applications to N-2 and CO-

TL;DR: In this paper, the multipartitioning form of the second-order many-body perturbation theory for state-selective effective Hamiltonians is adapted to stabilization calculations of temporary molecular anionic states.