The Mechanism of the Cathodic Hydrogen Evolution Reaction

1952 ◽  
Vol 99 (4) ◽  
pp. 169 ◽  
Author(s):  
J. O'M. Bockris ◽  
E. C. Potter
2016 ◽  
Vol 41 (8) ◽  
pp. 4660-4669 ◽  
Author(s):  
R. Garcia-Garcia ◽  
J.G. Rivera ◽  
R. Antaño-Lopez ◽  
F. Castañeda-Olivares ◽  
G. Orozco

Author(s):  
Mei Zhang ◽  
Zhongyao Duan ◽  
Lin Cui ◽  
Hongjie Yu ◽  
Ziqiang Wang ◽  
...  

Hybrid water electrolysis system composed of anodic urea oxidation reaction (UOR) and cathodic hydrogen evolution reaction (HER) has been regarded as a green and sustainable route to alleviate global energy...


Author(s):  
Zunjian Ke ◽  
Nicholas Williams ◽  
Xingxu Yan ◽  
Sabrina Younan ◽  
Dong He ◽  
...  

Renewable electricity-driven water splitting provides a pathway to manufacturing hydrogen as a promising alternative to fossil fuels. A typical water electrolysis device is comprised of a cathodic hydrogen evolution reaction...


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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