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2325038 
Journal Article 
Fenton chemistry at aqueous interfaces 
Enami, S; Sakamoto, Y; Colussi, AJ 
2014 
1 
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 0027-8424
EISSN: 1091-6490 
111 
2 
623-628 
English 
24379389 
WOS:000329614500026 
In a fundamental process throughout nature, reduced iron unleashes the oxidative power of hydrogen peroxide into reactive intermediates. However, notwithstanding much work, the mechanism by which Fe(2+) catalyzes H2O2 oxidations and the identity of the participating intermediates remain controversial. Here we report the prompt formation of O=Fe(IV)Cl3(-) and chloride-bridged di-iron O=Fe(IV) · Cl · Fe(II)Cl4(-) and O=Fe(IV) · Cl · Fe(III)Cl5(-) ferryl species, in addition to Fe(III)Cl4(-), on the surface of aqueous FeCl2 microjets exposed to gaseous H2O2 or O3 beams for <50 μs. The unambiguous identification of such species in situ via online electrospray mass spectrometry let us investigate their individual dependences on Fe(2+), H2O2, O3, and H(+) concentrations, and their responses to tert-butanol (an · OH scavenger) and DMSO (an O-atom acceptor) cosolutes. We found that (i) mass spectra are not affected by excess tert-butanol, i.e., the detected species are primary products whose formation does not involve · OH radicals, and (ii) the di-iron ferryls, but not O=Fe(IV)Cl3(-), can be fully quenched by DMSO under present conditions. We infer that interfacial Fe(H2O)n(2+) ions react with H2O2 and O3 >10(3) times faster than Fe(H2O)6(2+) in bulk water via a process that favors inner-sphere two-electron O-atom over outer-sphere one-electron transfers. The higher reactivity of di-iron ferryls vs. O=Fe(IV)Cl3(-) as O-atom donors implicates the electronic coupling of mixed-valence iron centers in the weakening of the Fe(IV)-O bond in poly-iron ferryl species. 
metal ions; reactive oxygen species; aerosols; advanced oxidation processes; nanoparticles