EXIDOS achieves chemical accuracy for multiple excited states in small molecules by variational optimization of low-energy subspaces using non-orthogonal Slater determinants without explicit orthogonality or symmetry constraints.
Title resolution pending
3 Pith papers cite this work. Polarity classification is still indexing.
3
Pith papers citing it
years
2026 3verdicts
UNVERDICTED 3representative citing papers
First NQS variational Monte Carlo calculation of excited states in A=4 nuclei and hypernuclei, reproducing benchmarks and providing the first ab initio M1 transition strength for ^{4}_ΛH consistent with weak-coupling limit at 1.3% suppression.
A reorganized Hartree-Fock framework imposes tunable orbital locality by pairing local degrees of freedom with local solution conditions, maintaining efficient SCF optimization and competitive reaction-energy accuracy.
citing papers explorer
-
Variational low-energy subspaces for chemically accurate excited states
EXIDOS achieves chemical accuracy for multiple excited states in small molecules by variational optimization of low-energy subspaces using non-orthogonal Slater determinants without explicit orthogonality or symmetry constraints.
-
Approximating Hartree-Fock theory via an efficiently local reformulation
A reorganized Hartree-Fock framework imposes tunable orbital locality by pairing local degrees of freedom with local solution conditions, maintaining efficient SCF optimization and competitive reaction-energy accuracy.