Electrochemical preparation of a novel, effective and low cast catalytic surface for hydrogen evolution reaction

2008 ◽  
Vol 33 (11) ◽  
pp. 2668-2678 ◽  
Author(s):  
B HABIBI ◽  
M POURNAGHIAZAR ◽  
H RAZMI ◽  
H ABDOLMOHAMMADZADEH
Author(s):  
Mi Luo ◽  
Jinyan Cai ◽  
Jiasui Zou ◽  
Zheng Jiang ◽  
Gongming Wang ◽  
...  

Since water dissociation and H desorption kinetics essentially determine the performance of alkaline hydrogen evolution reaction (HER), rationally regulating surface adsorption behavior to achieve superior catalytic surface is always challenging...


2020 ◽  
Vol 63 (11) ◽  
pp. 1563-1569
Author(s):  
Yanyan Fang ◽  
Da Sun ◽  
Shuwen Niu ◽  
Jinyan Cai ◽  
Yipeng Zang ◽  
...  

2017 ◽  
Vol 9 (50) ◽  
pp. 43674-43680 ◽  
Author(s):  
Kamran Akbar ◽  
Sajjad Hussain ◽  
Linh Truong ◽  
Sanjib Baran Roy ◽  
Jae Ho Jeon ◽  
...  

2020 ◽  
Vol 8 (44) ◽  
pp. 23323-23329
Author(s):  
Jing Hu ◽  
Siwei Li ◽  
Yuzhi Li ◽  
Jing Wang ◽  
Yunchen Du ◽  
...  

Crystalline–amorphous Ni–Ni(OH)2 core–shell assembled nanosheets exhibit outstanding electrocatalytic activity and stability for hydrogen evolution under alkaline conditions.


2020 ◽  
Author(s):  
Elisabeth Hofmeister ◽  
Jisoo Woo ◽  
Tobias Ullrich ◽  
Lydia Petermann ◽  
Kevin Hanus ◽  
...  

Cobaloximes and their BF<sub>2</sub>-bridged analogues have emerged as promising non-noble metal catalysts for the photocatalytic hydrogen evolution reaction (HER). Herein we report the serendipitous discovery that double complex salts such as [Co(dmgh)<sub>2</sub>py<sub>2</sub>]<sup>+</sup>[Co(dmgBPh<sub>2</sub>)<sub>2</sub>Cl<sub>2</sub>]<sup>-</sup> can be obtained in good yields by treatment of commercially available [Co(dmgh)<sub>2</sub>pyCl] with triarylboranes. A systematic study on the use of such double complex salts and their single salts with simple counterions as photocatalysts revealed HER activities comparable or superior to existing cobaloxime catalysts and suggests ample opportunities for this compound class in catalyst/photosensitizer dyads and immobilized architectures. Preliminary electrochemical and spectroscopic studies indicate that one key advantage of these charged cobalt complexes is that the reduction potentials as well as the electrostatic interaction with charged photosensitizers can be tuned.


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