Oxygen–Sulfur Exchange and the Gas-Phase Reactivity of Cobalt Sulfide Cluster Anions with Molecular Oxygen

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2014-09, Vol.118 (37), p.8163-8169
• Main Authors: Jia, Mei-Ye, Luo, Zhixun, He, Sheng-Gui, Ge, Mao-Fa
• Format: Article
• Language: English
• Subjects: Cobalt - chemistry; Models, Molecular; Molecular Conformation; Oxygen - chemistry; Sulfur - chemistry
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/jp500837g

We present here a study of gas-phase reactivity of cobalt sulfide cluster anions Co m S n – with molecular oxygen. Nascent Co m S n – clusters were prepared via a laser ablation source and reacted with oxygen in a fast flow reactor under thermal collision conditions. We chose 18O2 in place of 16O2 to avoid mass degeneration with sulfur, and a time-of-flight (TOF) mass spectrometer was used to detect the cluster distributions in the absence and presence of the reactant. It was found that oxygen–sulfur exchange occurs in the reactions for those with specific compositions (CoS) n – and (CoS) n S– (n = 2–5) according to a consistent pathway, “Co m S n – + 18O2 → Co m S n–1 18O– + S18O”. Typically, for “Co2S2 – + 18O2” we have calculated the reaction coordinates by employing the density functional theory (DFT), where both the oxygen–sulfur exchange and SO molecule release are thermodynamically and kinetically favorable. It is noteworthy that the reaction with molecular oxygen (triplet ground state) needs to overcome a spin excitation as well as a large O–O activation energy. This study sheds light on the activation of molecular oxygen by cobalt sulfides on one hand and also provides insight into the regeneration mechanism of cobalt oxides from the counterpart sulfides in the presence of oxygen gas on the other hand.