Photoselective isotope fractionation dynamics of N2 with cosmo and atmospheric chemistry perspectives

• 成果类型: Article
• 署名作者: Komarova, Ksenia; Gelfand, Natalia A.; Remacle, Francoise; Levine, Raphael D.; Chakraborty, Subrata; Jackson, Teresa L.; Kostko, Oleg; Thiemens, Mark H.
• 署名单位: Hebrew University of Jerusalem; University of Liege; University of California System; University of California Los Angeles; University of California Los Angeles Medical Center; David Geffen School of Medicine at UCLA; University of California System; University of California Los Angeles; University of California System; University of California San Diego; United States Department of Energy (DOE); Lawrence Berkeley National Laboratory; University of Southern California
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-13116
• DOI: 10.1073/pnas.2511172122
• 发表日期: 2025-07-22
• 关键词: excited-states; solar-system; photodissociation; oxygen; n-2; molecules; anomalies; carbon; atoms; co

摘要

Stable isotope ratio measurements provide valuable insights into a broad range of natural processes, from planetary atmospheres and climate to interstellar chemistry. Nitrogen, which has two stable isotopes, exhibits varying isotope ratios across the solar system. To model these observations, the isotope fraction as a function of energy is essential. At the Advanced Light Source (ALS), we measured the photodissociation of molecular nitrogen (N2) with vacuum UV photons where a single photon is sufficiently energetic to dissociate the strong bond. The nitrogen atoms produced are scavenged with H2 to form ammonia, whose isotopic makeup is determined. Blending the experiments with dynamical computations that include the shielding of light, we examine the isotopic composition and electronic atomic states produced. The measured photodissociation of N2 at a natural isotopic composition with a frequency broad light beam exceptionally strongly favors the formation of the heavier nitrogen isotope, 15N. Computations concur and suggest that the maximum in the quantum yield reflects significant variations in the specific electronic quantum states of the product N atoms that have quite different reactivities. Our quantum computations show that at similar energies, photodissociation of 14N14N and 15N14N can lead to different product channels. The computed dynamics include extensive state-selective spin-orbit and nonadiabatic couplings affecting the light absorption and dissociation pathways that proceed via the triplet manifold of states. Our results are relevant for future exploration missions, both in situ and sample-return and for other molecules such as O2 and CO.