collaborators

10 papers

physics.chem-ph2026

Nuclear-Electronic Quantum Dynamics in a Plasmonic Nanocavity

Jonathan H. Fetherolf, Tim Duong, Tao E. Li +1

Plasmonic nanocavities are a promising platform for strong light-matter coupling and enhanced spectroscopies at the single-molecule level. These nanoscale environments are challeng…

physics.chem-ph2026

Real-time nuclear-electronic orbital time-dependent density functional theory with a constrained traveling proton basis

Nicholas J. Boyer, Sharon Hammes-Schiffer

Nuclear quantum effects and non-Born--Oppenheimer effects play a vital role in many chemical and biological processes, motivating the incorporation of such effects into dynamical s…

physics.chem-ph2026

Extended Lagrangian molecular dynamics on vibronic surfaces in the nuclear-electronic orbital framework

Joseph A. Dickinson, Mathew Chow, Eno Paenurk +1

Proton transfer is central to many processes of chemical interest. The simulation of proton transfer dynamics requires the inclusion of nuclear quantum effects, such as zero-point…

cond-mat.supr-con2026

Capturing nuclear quantum effects in high-pressure superconducting hydrides and ice with nuclear-electronic orbital theory

Logan E. Smith, Paolo Settembri, Alessio Cucciari +3

Nuclear quantum effects are essential for correctly describing hydrogen-rich materials at high pressures. Superconducting hydrides and ice are prime examples of such systems, requi…

physics.chem-ph2026

Initialization with a Fock State Cavity Mode in Real-Time Nuclear--Electronic Orbital Polariton Dynamics

Millan F. Welman, Sharon Hammes-Schiffer

Molecular polaritons have drawn great interest in recent years as a possible avenue for providing optical control over chemical dynamics. A central challenge in the field is to ide…

physics.chem-ph2025

Nuclear-electronic orbital second-order coupled cluster for excited states

Jonathan H. Fetherolf, Fabijan Pavošević, Sharon Hammes-Schiffer

Excited-state methods within the nuclear--electronic orbital (NEO) framework have the potential to capture vibrational, electronic, and vibronic transitions in a single calculation…