Water Dissociation Kinetic‐Oriented Design of Nickel Sulfides via Tailored Dual Sites for Efficient Alkaline Hydrogen Evolution

2020 ◽  
pp. 2008578
Author(s):  
Jinsong Wang ◽  
Zhengfu Zhang ◽  
Haoran Song ◽  
Bao Zhang ◽  
Jia Liu ◽  
...  
2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Ruopeng Li ◽  
Hao Xu ◽  
Peixia Yang ◽  
Dan Wang ◽  
Yun Li ◽  
...  

AbstractTo achieve high efficiency of water electrolysis to produce hydrogen (H2), developing non-noble metal-based catalysts with considerable performance have been considered as a crucial strategy, which is correlated with both the interphase properties and multi-metal synergistic effects. Herein, as a proof of concept, a delicate NiCo(OH)x-CoyW catalyst with a bush-like heterostructure was realized via gas-template-assisted electrodeposition, followed by an electrochemical etching-growth process, which ensured a high active area and fast gas release kinetics for a superior hydrogen evolution reaction, with an overpotential of 21 and 139 mV at 10 and 500 mA cm−2, respectively. Physical and electrochemical analyses demonstrated that the synergistic effect of the NiCo(OH)x/CoyW heterogeneous interface resulted in favorable electron redistribution and faster electron transfer efficiency. The amorphous NiCo(OH)x strengthened the water dissociation step, and metal phase of CoW provided sufficient sites for moderate H immediate adsorption/H2 desorption. In addition, NiCo(OH)x-CoyW exhibited desirable urea oxidation reaction activity for matching H2 generation with a low voltage of 1.51 V at 50 mA cm−2. More importantly, the synthesis and testing of the NiCo(OH)x-CoyW catalyst in this study were all solar-powered, suggesting a promising environmentally friendly process for practical applications.


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 ◽  
Author(s):  
Hong Liu ◽  
Jian-Jun Wang ◽  
Li-Wen Jiang ◽  
Yuan Huang ◽  
Bing Bing Chen ◽  
...  

<p>Hydrogen production via alkaline water electrolysis is of significant interest. However, the additional water dissociation step makes the Volmer step a relatively more sluggish kinetics and consequently leads to a slower reaction rate than that in acidic solution. Herein, we demonstrate an effective strategy that Co(OH)<sub>2</sub> can promote the Volmer process by accelerating water dissociation and enhance the electrocatalytic performance of CoP toward alkaline hydrogen evolution reaction. The Co(OH)<sub>2</sub> nanoplates are electrochemically induced in-situ generated to form a nanotree-like structure with porous CoP nanowires, endowing the hybrid electrocatalyst with superior charge transportation, more exposed active sites, and enhanced reaction kinetics. This strategy may be extended to <a></a><a>other phosphides and chalcogenides </a>and provide insight into the design and fabrication of efficient alkaline HER catalysts.</p>


2020 ◽  
Vol 13 (9) ◽  
pp. 3110-3118 ◽  
Author(s):  
Zhao Li ◽  
Wenhan Niu ◽  
Zhenzhong Yang ◽  
Abdelkader Kara ◽  
Qi Wang ◽  
...  

The alkaline hydrogen evolution reaction (A-HER) holds great promise for clean hydrogen fuel generation but its practical utilization is severely hindered by the sluggish kinetics for water dissociation in alkaline solutions.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Xuesi Wang ◽  
Chaochen Xu ◽  
Mietek Jaroniec ◽  
Yao Zheng ◽  
Shi-Zhang Qiao

Abstract Most fundamental studies of electrocatalysis are based on the experimental and simulation results obtained for bulk model materials. Some of these mechanistic understandings are inapplicable for more active nanostructured electrocatalysts. Herein, considering the simplest and most typical electrocatalytic process, the hydrogen evolution reaction, an alternative reaction mechanism is proposed for nanomaterials based on the identification of a new intermediate, which differs from those commonly known for the bulk counterparts. In-situ Raman spectroscopy and electrochemical thermal/kinetic measurements were conducted on a series of nanomaterials under different conditions. In high-pH electrolytes with negligible hydronium (H3O+) concentration in bulk phase, massive H3O+ intermediates are found generating on the catalytic surface during water dissociation and hydrogen adsorption processes. These H3O+ intermediates create a unique acid-like local reaction environment on nanostructured catalytic surfaces and cut the energy barrier of the overall reaction. Such phenomena on nanostructured electrocatalysts explain their widely observed anomalously high activity under high-pH conditions.


2018 ◽  
Vol 5 (7) ◽  
pp. 1683-1689 ◽  
Author(s):  
Xiao Zhang ◽  
Pei Liu ◽  
Yanfang Sun ◽  
Tianrong Zhan ◽  
Qingyun Liu ◽  
...  

Hybrid electrocatalyst of ultrafine Pt particles anchored on a Ni3[Fe(CN)6]2 nanocube with low Pt loading of 4.0% is designed for HERs, and superior catalytic activity is obtained in both acidic and alkaline media because the Ni species remarkably facilitates the reaction kinetics of water dissociation and thus improves HER activity.


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