A systematic electronic structure study of the O–O bond dissociation energy of hydrogen peroxide and the electron affinity of the hydroxyl radical

• Published in: Theoretical chemistry accounts 2018-09, Vol.137 (9), p.1-11, Article 126
• Main Authors: Carmona, Danilo J., Contreras, David R., Douglas-Gallardo, Oscar A., Vogt-Geisse, Stefan, Jaque, Pablo, Vöhringer-Martinez, Esteban
• Format: Article
• Language: English
• Subjects: Affinity; Atomic/Molecular Structure and Spectra; Chemistry; Chemistry and Materials Science; Electron affinity; Electronic structure; Electrons; Energy of dissociation; Free energy; Functionals; Groundwater treatment; Heat of formation; Hydrogen peroxide; Hydrogen-based energy; Hydroxyl radicals; Inorganic Chemistry; Mathematical analysis; Organic Chemistry; Physical Chemistry; Regular Article; Theoretical and Computational Chemistry
• ISSN: 1432-881X; 1432-2234
• DOI: 10.1007/s00214-018-2307-z

Hydroxyl radical reduction and peroxide bond breaking in hydrogen peroxide are reactions involved in various processes such as the Fenton reaction, which has applications as e.g. groundwater remediation. Here, we study these two reactions from a thermodynamical point of view through the bond dissociation energy (BDE) of the O–O bond in hydrogen peroxide and the electron affinity (EA) of the hydroxyl radical. High-level ab-initio calculations at the complete basis set (CBS) limit were carried out, and the performance of different DFT-based methods was addressed by following a specific classification on the basis of the Jacob’s ladder in combination with various Pople’s basis sets. The ab-initio calculations at the CBS limit are in agreement with experimental reference data and identify a significant contribution of the electron correlation energy to the BDE and EA. The studied DFT-based methods were able to reproduce the ab-initio reference values, although no functional was particularly detected as the best for both reactions. The inclusion of certain percentage of Hartree–Fock (HF) exchange in DFT functionals leads in most cases to smaller BDE and EA values, which might be related to the poor description of the two reactions by the HF method. Considering the computational cost, DFT methods provide better BDE and EA values than HF methods with an accuracy comparable to the MP2 or CCSD level of theory. Additionally, the quality of the hydrogen peroxide, hydroxyl radical and hydroxyl anion structures obtained from these functionals was compared to experimental reference data. In general, bond lengths were well reproduced and the errors in the angles were between one and two degrees with some systematic trend with respect to the basis set’s size. From our results we conclude that DFT methods present a computationally less expensive alternative to describe these two reactions that play a role in the Fenton reaction. The benchmark that is carried out in this study provides a systematic validation of various approximated E xc [ ρ ] functionals combined with different basis sets, which could serve as a stepping-stone for future research on the Fenton reaction.