{
  "annotation_id": "fed4beac-33e5-47d7-9eaa-6484541009c5",
  "date_created": "2026-03-02T18:01:49.273000Z",
  "date_modified": "2026-03-02T18:01:49.273000Z",
  "file_hash": "e66b44caf0513b71c370e38cdbf89549e03abc21f0d73ed2fb78d792e33357f0",
  "private": false,
  "record": {
    "abstract": "We present an algebraic method for treating molecular vibrations in the Morse\npotential perturbed by an external laser field. By the help of a complete and\nnormalizable basis we transform the Schr\\\"{o}dinger equation into a system of\ncoupled ordinary differential equations. We apply our method to calculate the\ndissociation probability of the NO molecule excited by chirped laser pulses.\nThe dependence of the molecular dipole-moment on the interatomic separation is\ndetermined by a quantum-chemical method, and the corresponding transition\ndipole moments are given by approximate analytic expressions. These turn out to\nbe very small between neighboring stationary states around the vibrational\nquantum number $m=42$, therefore we propose to use additional pulses in order\nto skip this trapping state, and to obtain a reasonable dissociation\nprobability.",
    "arxiv_id": "quant-ph/0202069",
    "authors": [
      "Balazs Molnar",
      "Peter Foldi",
      "Mihaly G. Benedict",
      "Ferenc Bartha"
    ],
    "categories": [
      "quant-ph",
      "physics.atom-ph"
    ],
    "doi": "10.1209/epl/i2003-00328-9",
    "journal_ref": "Europhysics Lett. 61 (4): 445-451 FEB 2003",
    "title": "Time evolution in the Morse potential using supersymmetry: dissociation   of the NO molecule",
    "url": "https://arxiv.org/abs/quant-ph/0202069"
  },
  "schema_id": "dorsal/arxiv",
  "source": {
    "execution_id": "ae7996c7-1f25-4674-8698-344e1ce5dbf4",
    "id": "arXiv Dataset IDs",
    "type": "Model",
    "variant": "snapshot-2026-03-01",
    "version": "0.1.0"
  },
  "user_id": 1000002
}