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 ◽  
...  
2014 ◽  
Vol 1 (12) ◽  
pp. 2173-2173 ◽  
Author(s):  
Rasmus Frydendal ◽  
Elisa A. Paoli ◽  
Brian P. Knudsen ◽  
Björn Wickman ◽  
Paolo Malacrida ◽  
...  

Author(s):  
Taehyun Kwon ◽  
Heesu Yang ◽  
Minki Jun ◽  
Taekyung Kim ◽  
Jinwhan Joo ◽  
...  

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...


2016 ◽  
Vol 4 (8) ◽  
pp. 3153-3153 ◽  
Author(s):  
Charles R. Lhermitte ◽  
J. Garret Verwer ◽  
Bart M. Bartlett

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.


Catalysts ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1176
Author(s):  
Chau T. K. Nguyen ◽  
Ngoc Quang Tran ◽  
Thi Anh Le ◽  
Hyoyoung Lee

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.


2022 ◽  
Vol 9 ◽  
Author(s):  
Jiabiao Yan ◽  
Mingkun Xia ◽  
Chenguang Zhu ◽  
Dawei Chen ◽  
Fanglin Du

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.


2016 ◽  
Vol 4 (8) ◽  
pp. 2960-2968 ◽  
Author(s):  
Charles R. Lhermitte ◽  
J. Garret Verwer ◽  
Bart M. Bartlett

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).


Energies ◽  
2021 ◽  
Vol 14 (16) ◽  
pp. 5020
Author(s):  
Myung Jun Lee ◽  
Junyeop Kim ◽  
Jaeun Kang ◽  
Hyewon Shin ◽  
Junghwan Do ◽  
...  

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.


2019 ◽  
Vol 55 (63) ◽  
pp. 9347-9350 ◽  
Author(s):  
Lei Zhong ◽  
Yufei Bao ◽  
Xu Yu ◽  
Ligang Feng

An Fe doped NiTe bulk crystal was demonstrated to exhibit an extremely active and stable performance for the electrochemical oxygen evolution reaction.


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