Pentanuclear iron complex for water oxidation: Spectroscopic analysis of reactive intermediates in solution and catalyst immobilization into the MOF-based photoanode

• Published in: Journal of catalysis 2024-01, Vol.429 (C), p.115230, Article 115230
• Main Authors: Ezhov, Roman, Bury, Gabriel, Maximova, Olga, Daniel Grant, Elliot, Kondo, Mio, Masaoka, Shigeyuki, Pushkar, Yulia
• Format: Article
• Language: English
• Subjects: Electro catalysis; EPR; Reaction mechanisms; Water oxidation; X-ray absorption spectroscopy; X-ray emission spectroscopy
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2023.115230

[Display omitted] •The multinuclear Fe5 complex is highly active in electrocatalytic water oxidation.•Advanced in situ spectroscopic studies identify reactive intermediates of Fe5 cluster.•FeIV/ FeV oxidation states and Fe = O bond ∼ 1.6 Å are present during water oxidation.•FeO forms by expansion at 5-coordinate Fe with coordination of 6th water ligand.•Fe5-MIL-126 MOF composite is photoelectrocatalytic for water oxidation. Photoelectrochemical water splitting can produce green hydrogen for industrial use and CO2-neutral transportation, ensuring the transition from fossil fuels to green, renewable energy sources. The iron-based electrocatalyst [FeII4FeIII(μ-3-O)(μ-L)6]3+ (LH = 3,5-bis(2-pyridyl)pyrazole) (1), discovered in 2016, is one of the fastest molecular water oxidation catalysts (WOC) based on earth-abundant elements. However, its water oxidation reaction (WOR) mechanism has not been yet fully elucidated. Here, we present in situ X-ray spectroscopy and electron paramagnetic resonance (EPR) analysis of electrochemical WOR promoted by (1) in water-acetonitrile solution. We observed transient reactive intermediates during the in situ electrochemical WOR, consistent with a coordination sphere expansion prior to the onset of catalytic current. At a pre-catalytic (∼+1.1 V vs. Ag/AgCl) potential, the distinct g ∼ 2.0 EPR signal assigned to FeIII/FeIV interaction was observed. Prolonged bulk electrolysis at catalytic (∼+1.6 V vs. Ag/AgCl) potential leads to the further oxidation of Fe centers in (1). At the steady state achieved with such electrolysis, the formation of hypervalent FeVO and FeIVO catalytic intermediates was inferred with XANES and EXAFS fitting, detecting a short FeO bond at ∼ 1.6 Å. (1) was embedded into MIL-126 MOF with the formation of a (1)-MIL-126 composite. The latter was tested in photoelectrochemical WOR and demonstrated an increase in electrocatalytic current upon visible light irradiation in acidic (pH = 2) water solution. The presented spectroscopic analysis gives further insight into the catalytic pathways of multinuclear systems and should help the subsequent development of more energy- and cost-effective water-splitting catalysts based on earth-abundant metals. Photoelectrocatalytic activity of (1)-MIL-126 confirms the possibility of creating an assembly of (1) inside a solid support and harnessing solar irradiation towards industrial applications of the catalyst.