2023
DOI: 10.1039/d2cp05531g
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Lattice oxygen activation in disordered rocksalts for boosting oxygen evolution

Abstract: The recent development in some special oxygen evolution reaction (OER) electrocatalysts shows that the lattice oxygen could participate in the catalyzing process via lattice oxygen oxidation mechanism (LOM), which provides...

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Cited by 7 publications
(4 citation statements)
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References 42 publications
(55 reference statements)
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“…Except for the pH-dependent activity, the LOM can be indirectly proved by peroxo-like (O sensitive tetramethylammonium cation (TMA + ) into the electrolyte as a chemical detector to track the O 2 2À species during the LOM process. [45][46][47] We compared the OER activity of LSFC, NSFC, and PSFC electrodes in 1 M KOH and 1 M tetramethylammonium hydroxide (TMAOH) electrolytes, respectively. As shown in Fig.…”
Section: The Activity Origin and Oer Mechanismmentioning
confidence: 99%
“…Except for the pH-dependent activity, the LOM can be indirectly proved by peroxo-like (O sensitive tetramethylammonium cation (TMA + ) into the electrolyte as a chemical detector to track the O 2 2À species during the LOM process. [45][46][47] We compared the OER activity of LSFC, NSFC, and PSFC electrodes in 1 M KOH and 1 M tetramethylammonium hydroxide (TMAOH) electrolytes, respectively. As shown in Fig.…”
Section: The Activity Origin and Oer Mechanismmentioning
confidence: 99%
“…In detail, one is the CPET process; the other involves a nonconcerted proton-electron transfer step, where the decoupled proton transfer is highly constrained by the pH level of the electrolyte. [80][81][82] Such a pH-dependent OER activity on the reversible hydrogen electrode (RHE) scale stems from the mismatch between electron-transfer kinetics and OH − affinity at theelectrocatalyst/electrolyte interface. [83,84] Compared to the AEM-based electrocatalyst, the LOM process typically exhibits pH dependence at the RHE scale due to the thermodynamic instability of the bulk phase of LOM-based catalyst under operando OER conditions irrespective of the pH value and the decreased charge-transfer energy that shields charges at the catalyst/electrolyte interface via the introduction of ligand holes into the O 2p band, weakening the OH − adsorption.…”
Section: Experimental Observations For Lommentioning
confidence: 99%
“…Furthermore, recent studies have proposed a new mechanism for the OER based on redox chemistry, defined as a lattice oxidation mechanism (LOM). In this mechanism, the lattice oxygen could be activated at the corresponding potential and could participate in the formation of O-O active intermediates during the OER [42][43][44].…”
Section: Electrochemical Evaluationmentioning
confidence: 99%