scholarly journals Inside Back Cover: Benchmarking the Stability of Oxygen Evolution Reaction Catalysts: The Importance of Monitoring Mass Losses (ChemElectroChem 12/2014)

2014 ◽  
Vol 1 (12) ◽  
pp. 2173-2173 ◽  
Author(s):  
Rasmus Frydendal ◽  
Elisa A. Paoli ◽  
Brian P. Knudsen ◽  
Björn Wickman ◽  
Paolo Malacrida ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Back Cover ◽  
Mass Losses ◽  
The Stability

scholarly journals Benchmarking the Stability of Oxygen Evolution Reaction Catalysts: The Importance of Monitoring Mass Losses

2014 ◽  
Vol 1 (12) ◽  
pp. 2075-2081 ◽  
Author(s):  
Rasmus Frydendal ◽  
Elisa A. Paoli ◽  
Brian P. Knudsen ◽  
Björn Wickman ◽  
Paolo Malacrida ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Mass Losses ◽  
The Stability

Interfacing RuO2 with Pt to induce efficient charge transfer from Pt to RuO2 for highly efficient and stable oxygen evolution under acidic media

2021 ◽  
Author(s):  
Taehyun Kwon ◽  
Heesu Yang ◽  
Minki Jun ◽  
Taekyung Kim ◽  
Jinwhan Joo ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Acidic Media ◽  
Highly Efficient ◽  
Efficient Charge ◽  
Stable Oxygen ◽  
The Stability

The oxygen evolution reaction (OER) requires a large overpotential which undermines the stability of electrocatalysts, typically IrOx or RuOx. RuOx is particularly vulnerable to high overpotential in acidic media, due...

scholarly journals Inside Back Cover: Effect of Adding CeO2to RuO2-IrO2Mixed Nanocatalysts: Activity towards the Oxygen Evolution Reaction and Stability in Acidic Media (ChemElectroChem 8/2015)

2015 ◽  
Vol 2 (8) ◽  
pp. 1206-1206
Author(s):  
Thomas Audichon ◽  
Sophie Morisset ◽  
Teko W. Napporn ◽  
K. Boniface Kokoh ◽  
Clément Comminges ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Acidic Media ◽  
Back Cover

scholarly journals Correction: Improving the stability and selectivity for the oxygen-evolution reaction on semiconducting WO3 photoelectrodes with a solid-state FeOOH catalyst

2016 ◽  
Vol 4 (8) ◽  
pp. 3153-3153 ◽  
Author(s):  
Charles R. Lhermitte ◽  
J. Garret Verwer ◽  
Bart M. Bartlett
Keyword(s):  
Solid State ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
The Stability

Correction for ‘Improving the stability and selectivity for the oxygen-evolution reaction on semiconducting WO3 photoelectrodes with a solid-state FeOOH catalyst’ by Charles R. Lhermitte et al., J. Mater. Chem. A, 2016, DOI: 10.1039/c5ta04747a.

scholarly journals Covalently Bonded Ir(IV) on Conducted Blue TiO2 for Efficient Electrocatalytic Oxygen Evolution Reaction in Acid Media

Catalysts ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1176
Author(s):  
Chau T. K. Nguyen ◽  
Ngoc Quang Tran ◽  
Thi Anh Le ◽  
Hyoyoung Lee
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Acid Media ◽  
Covalent Bonds ◽  
Covalently Bonded ◽  
Tiny Amount ◽  
Primary Obstacle ◽  
Anode Electrode ◽  
Mass Activity ◽  
The Stability

The stability of anode electrode has been a primary obstacle for the oxygen evolution reaction (OER) in acid media. We design Ir-oxygen of hydroxyl-rich blue TiO2 through covalent bonds (Ir–O2–2Ti) and investigate the outcome of favored exposure of different amounts of covalent Ir–oxygen linked to the conductive blue TiO2 in the acidic OER. The Ir-oxygen-blue TiO2 nanoclusters show a strong synergy in terms of improved conductivity and tiny amount usage of Ir by using blue TiO2 supporter, and enhanced stability using covalent Ir-oxygen-linking (i.e., Ir oxide) in acid media, leading to high acidic OER performance with a current density of 10 mA cm−2 at an overpotential of 342 mV, which is much higher than that of IrO2 at 438 mV in 0.1 M HClO4 electrolyte. Notably, the Ir–O2–2Ti has a great mass activity of 1.38 A/mgIr at an overpotential 350 mV, which is almost 27 times higher than the mass activity of IrO2 at the same overpotential. Therefore, our work provides some insight into non-costly, highly enhanced, and stable electrocatalysts for the OER in acid media.

scholarly journals Perovskite With Tunable Active-Sites Oxidation State by High-Valence W for Enhanced Oxygen Evolution Reaction

2022 ◽  
Vol 9 ◽  
Author(s):  
Jiabiao Yan ◽  
Mingkun Xia ◽  
Chenguang Zhu ◽  
Dawei Chen ◽  
Fanglin Du
Keyword(s):  
Electronic Structure ◽  
Water Splitting ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Precious Metal ◽  
Active Sites ◽  
Perovskite Oxides ◽  
Intrinsic Activity ◽  
Excellent Activity ◽  
The Stability

Perovskite oxides have been established as a promising kind of catalyst for alkaline oxygen evolution reactions (OER), because of their regulated non-precious metal components. However, the surface lattice is amorphous during the reaction, which gradually decreases the intrinsic activity and stability of catalysts. Herein, the precisely control tungsten atoms substituted perovskite oxides (Pr0.5Ba0.5Co1-xWxO3-δ) nanowires were developed by electrostatic spinning. The activity and Tafel slope were both dependent on the W content in a volcano-like fashion, and the optimized Pr0.5Ba0.5Co0.8W0.2O3-δ exhibits both excellent activity and superior stability compared with other reported perovskite oxides. Due to the outermost vacant orbitals of W6+, the electronic structure of cobalt sites could be efficiently optimized. Meanwhile, the stronger W-O bond could also significantly improve the stability of latticed oxide atoms to impede the generation of surface amorphous layers, which shows good application value in alkaline water splitting.

Improving the stability and selectivity for the oxygen-evolution reaction on semiconducting WO3 photoelectrodes with a solid-state FeOOH catalyst

2016 ◽  
Vol 4 (8) ◽  
pp. 2960-2968 ◽  
Author(s):  
Charles R. Lhermitte ◽  
J. Garret Verwer ◽  
Bart M. Bartlett
Keyword(s):  
Solid State ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Sol Gel ◽  
Electrode Stability ◽  
The Stability

WO3 electrodes were synthesized via a sol–gel route followed by the photoelectrochemical deposition of a solid state FeOOH oxygen-evolution catalyst (OEC) to observe its effects on electrode stability and selectivity towards the oxygen evolution reaction (OER).

scholarly journals Electrocatalytic Activity of Reduced Graphene Oxide Supported Cobalt Cinnamate for Oxygen Evolution Reaction

Energies ◽  
2021 ◽  
Vol 14 (16) ◽  
pp. 5020
Author(s):  
Myung Jun Lee ◽  
Junyeop Kim ◽  
Jaeun Kang ◽  
Hyewon Shin ◽  
Junghwan Do ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Electrocatalytic Activity ◽  
Electrochemical Reaction ◽  
Porous Coordination Polymers ◽  
Inorganic Hybrid ◽  
Reduced Graphene ◽  
The Stability

The stability of porous coordination polymers during an electrochemical reaction could be improved by introducing supporter materials. An I3O0-type inorganic hybrid electrocatalyst, cobalt cinnamate, supported on reduced graphene oxide (rGO) was successfully prepared for an oxygen evolution reaction. The electrocatalytic activity and stability of cobalt cinnamate(catalyst)/rGO composite were significantly improved due to the strong interaction between catalyst and supporter, which led to enhanced anchoring stability and electrical conductivity. The catalyst/rGO composite shows ~30 mV reduction in overpotential and improvement in durability from ≥35% to ≥70% after a reaction time of 12 h, compared to the catalyst alone.

scholarly journals Back Cover: In Situ Tetraethoxysilane-Templated Porous Ba0.5Sr0.5Co0.8Fe0.2O3−δPerovskite for the Oxygen Evolution Reaction (ChemElectroChem 2/2015)

2014 ◽  
Vol 2 (2) ◽  
pp. 292-292
Author(s):  
Yisu Yang ◽  
Wei Zhou ◽  
Ruochen Liu ◽  
Mengran Li ◽  
Thomas E. Rufford ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Back Cover
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