2019
DOI: 10.1016/j.chempr.2019.10.011
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Dissolution-Induced Surface Roughening and Oxygen Evolution Electrocatalysis of Alkaline-Earth Iridates in Acid

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Cited by 118 publications
(109 citation statements)
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“…The surface atoms at the electrode(electrocatalyst)/electrolyte interface under acidic/alkaline water oxidation condition are dynamically changed in their structural integrity. [ 48,52,54,108,109 ] Based on the structural features of the electrocatalysts, the dissolution of electrocatalyst components along with the applied potential originates the surface reconstruction and triggers structure evolution, resulting in enhanced OER performance. Specifically, the dynamic reconstruction of perovskite‐, spinel‐, and mixed metal alloy‐/oxide‐based OER electrocatalysts due to the dissolution of electrocatalyst component are discussed in this section.…”
Section: Synthesis Of Reconstructed Electrocatalysts For Oermentioning
confidence: 99%
See 1 more Smart Citation
“…The surface atoms at the electrode(electrocatalyst)/electrolyte interface under acidic/alkaline water oxidation condition are dynamically changed in their structural integrity. [ 48,52,54,108,109 ] Based on the structural features of the electrocatalysts, the dissolution of electrocatalyst components along with the applied potential originates the surface reconstruction and triggers structure evolution, resulting in enhanced OER performance. Specifically, the dynamic reconstruction of perovskite‐, spinel‐, and mixed metal alloy‐/oxide‐based OER electrocatalysts due to the dissolution of electrocatalyst component are discussed in this section.…”
Section: Synthesis Of Reconstructed Electrocatalysts For Oermentioning
confidence: 99%
“…[ 23,43,45 ] Also, the reconstruction process changes the surface of electrocatalysts reversibly or irreversibly depending on their structural features. [ 48–58 ] For example, the Co 3 O 4 electrocatalyst self‐reconstructed into amorphous CoO x (OH) y (di‐ u ‐oxobridged Co 3+/4+ ) under OER potential region can be reverted to the original structure when returning the potential to the non‐OER region . [ 59 ] Conversely, noble metal‐based electrocatalysts, transition metal‐based oxides and nonoxides (e.g., chalcogenides, pnictides, carbides, etc.)…”
Section: Introductionmentioning
confidence: 99%
“…expense of its easy corrosion. [14] Additionally, until now SrIrO 3 can only be prepared in the forms of thin films supported on catalytically-inert perovskite substrates [15][16][17] and free-standing, micrometer-scaled particles. [18] As a result, this perovskite material typically suffers from low surface areas and limited available catalytic active sites, which are detrimental to transferring its good specific activity to a real electrocatalyst with high mass activity.…”
Section: Doi: 101002/adma202001430mentioning
confidence: 99%
“…[ 21,25,26 ] In contrast, the kinetics of the electrode reactions in acidic solutions are much faster than that in alkaline and neutral ones due to the higher proton transfer rate between anode and cathode. [ 27–30 ] For example, a water electrolyzer with proton exchange membrane (PEM) in acidic solutions can reach up to 800–2500 mA cm −2 at 70–80 °C, while the one with anion exchange membrane in alkaline solutions delivers much lower current density of 200–500 mA cm −2 at 50–70 °C. [ 8,9 ] In addition, the operation voltages of PEM electrolyzers are lower than that with anion exchange membranes, due to their lower overpotentials on both anode and cathode.…”
Section: Introductionmentioning
confidence: 99%