scholarly journals Understanding the formation of bulk- and surface-active layered (oxy)hydroxides for water oxidation starting from a cobalt selenite precursor

2020 ◽  
Vol 13 (10) ◽  
pp. 3607-3619
Author(s):  
Jan Niklas Hausmann ◽  
Stefan Mebs ◽  
Konstantin Laun ◽  
Ingo Zebger ◽  
Holger Dau ◽  
...  

Starting from a cobalt selenite precatalyst, we obtained a bulk and a near-surface active oxygen evolution catalyst and connected their structural properties to the precatalyst structure, the transformation conditions, and the catalytic activity.

Nanoscale ◽  
2021 ◽  
Author(s):  
Bing Fu ◽  
Zhijiao Wu ◽  
Kai Guo ◽  
Lingyu Piao

Owing to their scientific and technological importance, the development of highly efficient photocatalytic water oxidation systems with rapid photogenerated charge separation and high surface catalytic activity has highly desirable for...


2015 ◽  
Vol 8 (6) ◽  
pp. 1719-1724 ◽  
Author(s):  
Yayuan Liu ◽  
Haotian Wang ◽  
Dingchang Lin ◽  
Chong Liu ◽  
Po-Chun Hsu ◽  
...  

Electrochemical lithium tuning of olivine-type lithium transition metal phosphates results in greatly enhanced oxygen evolution catalytic activity.


2018 ◽  
Vol 11 (7) ◽  
pp. 1736-1741 ◽  
Author(s):  
Juzhe Liu ◽  
Yongfei Ji ◽  
Jianwei Nai ◽  
Xiaogang Niu ◽  
Yi Luo ◽  
...  

A simple strategy to synthesize ultrathin, amorphous and alloyed structural cobalt–vanadium hydr(oxy)oxide catalysts with enhanced water oxidation catalytic activity.


2017 ◽  
Vol 1 (4) ◽  
pp. 780-788 ◽  
Author(s):  
Suoyuan Lian ◽  
Michelle P. Browne ◽  
Carlota Domínguez ◽  
Serban N. Stamatin ◽  
Hugo Nolan ◽  
...  

Solvothermally synthesised MnCO3 leads to template-free formation of highly porous, defect-rich MnO2 with high activity in water oxidation.


2021 ◽  
Author(s):  
Yuwei Jin ◽  
Wenjing Huo ◽  
Libin Zhang ◽  
Yong Li ◽  
Qianqian Chen ◽  
...  

The tunable oxygen vacancies of LaNiO3 (LNO-Vo) is realized by the theoretical prediction and NaBH4-reduction approach. The LNO2.7 catalyst exhibits superior catalytic activity and long-time stability for water oxidation. A...


2019 ◽  
Vol 43 (27) ◽  
pp. 10868-10877 ◽  
Author(s):  
Xuejun Zhang ◽  
Min Zhao ◽  
Zhongxian Song ◽  
Heng Zhao ◽  
Wei Liu ◽  
...  

The Co–La catalyst was used to the catalytic oxidation of toluene. The LaCoO3 perovskite was detected. The abundance of Co3+ and active oxygen contributed synergistically to the redox cycle reaction, which could improve the catalytic activity.


2018 ◽  
Vol 54 (43) ◽  
pp. 5462-5465 ◽  
Author(s):  
Jinxiu Zhao ◽  
Xianghong Li ◽  
Guanwei Cui ◽  
Xuping Sun

An Fe-doped NiCr2O4 nanoparticle film on Ni foam (Fe–NiCr2O4/NF) acts as a durable water oxidation electrocatalyst with superior activity, needing an overpotential of 318 mV to drive 500 mA cm−2 in 1.0 M KOH.


2016 ◽  
Vol 52 (21) ◽  
pp. 4068-4071 ◽  
Author(s):  
Alexander Weremfo ◽  
Xunyu Lu ◽  
Paul Carter ◽  
D. Brynn Hibbert ◽  
Chuan Zhao

The use of a central composite design to model the roughness of an electrochemically roughened Pt electrode and the surface with a well-defined nanostructure exhibits greatly improved catalytic activity towards oxygen evolution reaction.


Author(s):  
Alberto Bucci ◽  
Suvendu Sekhar Mondal ◽  
Vlad Martin-Diaconescu ◽  
Alexandr Shafir ◽  
Julio Lloret-Fillol

<p>A family of three imidazolate-based Co-MOFs, IFP-5, -8 and -10 (Imidazolate Framework Potsdam), with different peripheral group –R (-Me, -OMe and –OEt, respectively) have been synthesized by a solvothermal method and tested toward oxygen evolution reaction (OER). Remarkably, IFP-8 presents low overpotentials (319 mV at 10 mA/cm<sup>2</sup>, and 490 mV at 500 mA/cm<sup>2</sup>) and extraordinary stability during 120 h, even when used as a catalyst toward overall water splitting reaction. An integrated <i>ex-situ</i> spectroscopic study, based on PXRD, EXAFS, and ATR, allows the identification of the active species and the factors that rule the catalytic activity. Indeed, it was found that the performances are highly affected by the nature of the -R group, because this small change strongly influences the conversion of the initial MOF to the active species. As a consequence, the remarkable activity of IFP-8 can be ascribed to the formation of Co(O)OH phase of few nanometers particle size (3-10 nm) during the electrocatalytic oxygen evolution. </p>


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