2020
DOI: 10.1016/j.jcat.2020.05.008
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Oxygen evolution electrocatalysis using mixed metal oxides under acidic conditions: Challenges and opportunities

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Cited by 71 publications
(45 citation statements)
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“…Two well-accepted possible catalytic mechanisms for OER have been proposed, adsorbate evolution mechanism (AEM) and lattice oxygen participation mechanism (LOM). [33][34][35][36] Typically for AEM, the formation of absorbed *OH intermediate, its transformation to *O, active *OOH formation and the final oxygen molecule release are the key successive steps. Furthermore, no matter what mechanism follows, the catalyst structures especially for local oxygen species structure are very crucial for a complete four-electron involved catalytic cycle.…”
Section: Application Of Ceo 2 -Based Electrocatalysts In Oermentioning
confidence: 99%
See 1 more Smart Citation
“…Two well-accepted possible catalytic mechanisms for OER have been proposed, adsorbate evolution mechanism (AEM) and lattice oxygen participation mechanism (LOM). [33][34][35][36] Typically for AEM, the formation of absorbed *OH intermediate, its transformation to *O, active *OOH formation and the final oxygen molecule release are the key successive steps. Furthermore, no matter what mechanism follows, the catalyst structures especially for local oxygen species structure are very crucial for a complete four-electron involved catalytic cycle.…”
Section: Application Of Ceo 2 -Based Electrocatalysts In Oermentioning
confidence: 99%
“…To circumvent these obstacles, opening up new opportunities to develop advanced electrocatalysts is very promising. Two well‐accepted possible catalytic mechanisms for OER have been proposed, adsorbate evolution mechanism (AEM) and lattice oxygen participation mechanism (LOM) [33–36] . Typically for AEM, the formation of absorbed *OH intermediate, its transformation to *O, active *OOH formation and the final oxygen molecule release are the key successive steps.…”
Section: Application Of Ceo2‐based Electrocatalysts In Oermentioning
confidence: 99%
“…For example, industrial electrolytic water generally maintains the external voltage at 1.8~2.0 V [16]. Typically, the descriptor of overpotential is used to show the difference between the thermodynamic potential and the practical potential required to drive the electrochemical reaction [24]. The overpotential mainly comes from the electrochemical polarization on the anode side (η a ) and cathode side (η c ) and the ohmic polarization caused by other resistors (η other ) [25].…”
Section: H O L → O + 4h + 4ementioning
confidence: 99%
“…In the case of the OER in acid media, two possible mechanisms built on consecutive proton and electron transfers during the catalytic cycle, known as the adsorbate evolution mechanism (AEM) and the lattice oxygen participation mechanism (LOM), have been widely accepted [24,26,54,55] (Figure 2). For the reaction path based on the AEM, a water molecule first adsorbs on a surface metal cation and decomposes into a proton (H + ) to form HO*, which further dissociates the second proton to form O* in the second step.…”
Section: Mechanisms For the Oer In Acidic Mediamentioning
confidence: 99%
“…The reduction of H + ions occurs at the cathode (2H + (aq) + 2e - H2 (g)) and the oxidation of water takes place at the anode (2H2O(l)  O2(g) + 4H + (aq) + 4e -) 5,20 . The thermodynamic voltage of water splitting is 1.23 V at 25 °C and 1 atm which corresponds to an energy input of G = 237.1 kJ mol - 1 12,21 , but much higher potentials-referred as overpotential-are required to initiate practical water splitting 22,23 .…”
Section: Introductionmentioning
confidence: 99%