Understanding Structure-Dependent Catalytic Performance of Nickel Selenides for Electrochemical Water Oxidation

ACS Catalysis ◽  
2016 ◽  
Vol 7 (1) ◽  
pp. 310-315 ◽  
Author(s):  
Kun Xu ◽  
Hui Ding ◽  
Haifeng Lv ◽  
Shi Tao ◽  
Pengzuo Chen ◽  
...  

2020 ◽  
Vol 234 (5) ◽  
pp. 925-978 ◽  
Author(s):  
Jens Melder ◽  
Peter Bogdanoff ◽  
Ivelina Zaharieva ◽  
Sebastian Fiechter ◽  
Holger Dau ◽  
...  

AbstractThe efficient catalysis of the four-electron oxidation of water to molecular oxygen is a central challenge for the development of devices for the production of solar fuels. This is equally true for artificial leaf-type structures and electrolyzer systems. Inspired by the oxygen evolving complex of Photosystem II, the biological catalyst for this reaction, scientists around the globe have investigated the possibility to use manganese oxides (“MnOx”) for this task. This perspective article will look at selected examples from the last about 10 years of research in this field. At first, three aspects are addressed in detail which have emerged as crucial for the development of efficient electrocatalysts for the anodic oxygen evolution reaction (OER): (1) the structure and composition of the “MnOx” is of central importance for catalytic performance and it seems that amorphous, MnIII/IV oxides with layered or tunnelled structures are especially good choices; (2) the type of support material (e.g. conducting oxides or nanostructured carbon) as well as the methods used to immobilize the MnOx catalysts on them greatly influence OER overpotentials, current densities and long-term stabilities of the electrodes and (3) when operating MnOx-based water-oxidizing anodes in electrolyzers, it has often been observed that the electrocatalytic performance is also largely dependent on the electrolyte’s composition and pH and that a number of equilibria accompany the catalytic process, resulting in “adaptive changes” of the MnOx material over time. Overall, it thus has become clear over the last years that efficient and stable water-oxidation electrolysis by manganese oxides can only be achieved if at least four parameters are optimized in combination: the oxide catalyst itself, the immobilization method, the catalyst support and last but not least the composition of the electrolyte. Furthermore, these parameters are not only important for the electrode optimization process alone but must also be considered if different electrode types are to be compared with each other or with literature values from literature. Because, as without their consideration it is almost impossible to draw the right scientific conclusions. On the other hand, it currently seems unlikely that even carefully optimized MnOx anodes will ever reach the superb OER rates observed for iridium, ruthenium or nickel-iron oxide anodes in acidic or alkaline solutions, respectively. So at the end of the article, two fundamental questions will be addressed: (1) are there technical applications where MnOx materials could actually be the first choice as OER electrocatalysts? and (2) do the results from the last decade of intensive research in this field help to solve a puzzle already formulated in 2008: “Why did nature choose manganese to make oxygen?”.



2015 ◽  
Vol 185 ◽  
pp. 87-104 ◽  
Author(s):  
Lianpeng Tong ◽  
Ruifa Zong ◽  
Rongwei Zhou ◽  
Nattawut Kaveevivitchai ◽  
Gang Zhang ◽  
...  

A series of RuII complexes that behave as water oxidation catalysts were prepared involving a tetradentate equatorial ligand and two 4-substituted pyridines as the axial ligands. Two of these complexes were derived from 2,9-di-(pyrid-2′-yl)-1,10-phenanthroline (dpp) and examine the effect of incorporating electron-donating amino and bulky t-butyl groups on catalytic activity. A third complex replaced the two distal pyridines with N-methylimidazoles that are more electron-donating than the pyridines of dpp and potentially stabilize higher oxidation states of the metal. The tetradentate ligand 2-(pyrid-2′-yl)-6-(1′′,10′′-phenanthrol-2′′-yl)pyridine (bpy–phen), possessing a bonding cavity similar to dpp, was also prepared. The RuII complex of this ligand does not have two rotatable pyridines in the equatorial plane and thus shows different flexibility from the [Ru(dpp)] complexes. All the complexes showed activity towards water oxidation. Investigation of their catalytic behavior and electrochemical properties suggests that they may follow the same catalytic pathway as the prototype [Ru(dpp)pic2]2+ involving a seven-coordinated [RuIV(O)] intermediate. The influence of coordination geometry on catalytic performance is analyzed and discussed.



2017 ◽  
Vol 5 (33) ◽  
pp. 17609-17618 ◽  
Author(s):  
D. Ruchira Liyanage ◽  
Da Li ◽  
Quintin B. Cheek ◽  
Habib Baydoun ◽  
Stephanie L. Brock

Incorporation of Ru into Ni2P nanoparticles moderates the redox behavior of Ni and lowers the kinetic barrier for water oxidation.



2020 ◽  
Vol 56 (62) ◽  
pp. 8750-8753 ◽  
Author(s):  
Ying Wang ◽  
Shiqi Wang ◽  
Dayan Liu ◽  
Lin Zhou ◽  
Ran Du ◽  
...  

Herein, a normal-pulse-voltage-assisted method is proposed for preparation of high quality graphene-wrapped CuO nanoflowers on CF. The as-obtained CuO NF@G/CF electrode exhibits a competitive OER catalytic performance in 1.0 M KOH solution.



Author(s):  
Jing-Hong Lian ◽  
Hongyi Tan ◽  
Changqing Guo ◽  
Li-sha Shen ◽  
Zhuo-Xin Lu ◽  
...  

The inactivation of molybdenum carbide catalyst by water oxidation is a significant problem in steam reforming of dimethyl ether (SRD) reaction. In this work, the catalytic performance and stability of...



2019 ◽  
Vol 241 ◽  
pp. 31-34
Author(s):  
Anitha Devadoss ◽  
Subramaniyan Ramasundaram ◽  
K. Asokan ◽  
Byungki Kim ◽  
Sudhagar Pitchaimuthu




2012 ◽  
Vol 51 (6) ◽  
pp. 3388-3398 ◽  
Author(s):  
Lianpeng Tong ◽  
Ying Wang ◽  
Lele Duan ◽  
Yunhua Xu ◽  
Xiao Cheng ◽  
...  


2016 ◽  
Vol 4 (34) ◽  
pp. 13133-13141 ◽  
Author(s):  
Xinzhe Li ◽  
Yiyun Fang ◽  
Shiling Zhao ◽  
Juntian Wu ◽  
Feng Li ◽  
...  

Nitrogen-doped mesoporous carbon nanosheet/carbon nanotube hybrids are prepared. This metal-free catalyst exhibits remarkable catalytic performance for both OER and ORR in 0.1 M KOH solution.





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