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Projected Complex Absorbing Potential Multireference Configuration Interaction Approach for Shape and Feshbach Resonances.

作者信息

Thodika Mushir, Matsika Spiridoula

机构信息

Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122, United States.

出版信息

J Chem Theory Comput. 2022 Jun 14;18(6):3377-3390. doi: 10.1021/acs.jctc.1c01310. Epub 2022 May 27.

Abstract

Anion resonances are formed as metastable intermediates in low-energy electron-induced reactions. Due to the finite lifetimes of resonances, applying standard Hermitian formalism for their characterization presents a vexing problem for computational chemists. Numerous modifications to conventional quantum chemical methods have enabled satisfactory characterization of resonances, but specific issues remain, especially in describing two-particle one-hole (2p-1h) resonances. An accurate description of these resonances and their coupling with single-particle resonances requires a multireference approach. We propose a projected complex absorbing potential (CAP) implementation within the multireference configuration interaction (MRCI) framework to characterize single-particle and 2p-1h resonances. As a first application, we use the projected-CAP-MRCI approach to characterize and benchmark the Π shape resonance in N. We test its performance as a function of the size of the subspace and other parameters, and we compute the complex potential energy surface of the Π shape resonance to show that a smooth curve is obtained. One key benefit of MRCI is that it can describe Feshbach resonances (most common examples of 2p-1h resonances) at the same footing as shape resonances. Therefore, it is uniquely positioned to describe mixing between the different channels. To test these additional capabilities, we compute Feshbach resonances in HO and anions of dicyanoethylene isomers. We find that CAP-MRCI can efficiently capture the mixing between the Feshbach and shape resonances in dicyanoethylene isomers, which has significant consequences for their lifetimes.

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