Corrigendum to “Elastic-plastic bending properties of an AZ31B magnesium alloy based on persistent tensile preloads” [J. Alloys Compd. 708 (2017) 594–599]

Two Dimensional Ir‐Based Catalysts for Acidic OER

“…Recently, the metastable phase IrO 2 was reported, which shows special performance in acidic OER due to its unique coordination mode and surface structure. [ 57 ]…”

“…Recently, the metastable phase IrO 2 was reported, which shows special performance in acidic OER due to its unique coordination mode and surface structure. [57] In 2021, Shao's group first reported a new metastable 1T phase IrO 2 . [14a] The SEM image in Figure 2v shows a flexible iridium oxide nanosheet.…”

“…It was found that the change in the overpotential of the catalyst was very small after 2 h of testing. [57] In 2018, Daniel et al tested the acidic OER performance of an iridium oxide coating in 0.1 m HClO 4 and found that the overpotential when the catalyst current density reached 10 mA cm −2 was 344 mV. The slope of the Tafel is 58 mV dec −1 .…”

Coupling Adsorbed Evolution and Lattice Oxygen Mechanism in Fe‐Co(OH)2/Fe2O3 Heterostructure for Enhanced Electrochemical Water Oxidation

“…[23] ii) The dynamic formation and accelerated migration of lattice oxygen vacancies can induce the uncoordinated metal ion, resulting in the dissolved leaching of metal ions as well as the structural reconstruction and deactivation of the bulk phase, which seriously affects the stability of the catalyst. [24] To address the aforementioned critical aspects, a proof-ofconcept Fe-Co(OH) 2 /Fe 2 O 3 heterostructure as a surface model catalyst was constructed, where Fe-Co(OH) 2 and Fe 2 O 3 follow AEM mechanism and LOM mechanism, respectively, so that Fe-Co(OH) 2 can complete rapidly deprotonation process due to their stronger adsorption for *OH/*O on metal site while Fe 2 O 3 can trigger O─O coupling step in lattice oxygen site. The density functional theory (DFT) theoretical calculation and chemical probe experiment identify the probable coupling mechanism of AEM and LOM.…”

“…[ 23 ] ii) The dynamic formation and accelerated migration of lattice oxygen vacancies can induce the uncoordinated metal ion, resulting in the dissolved leaching of metal ions as well as the structural reconstruction and deactivation of the bulk phase, which seriously affects the stability of the catalyst. [ 24 ]…”