Photoelectrochemical Supercontinuum Solar Light Zero Bias Hydrogen Generation with Membrane-Based Cells Designed for Decreasing Overall Water Electrolysis Voltage and Water Dissociation (23)

2019 ◽  
Keyword(s):  
Hydrogen Generation ◽  
Water Electrolysis ◽  
Solar Light ◽  
Water Dissociation ◽  
Zero Bias

(Invited) Photoelectrochemical Hydrogen Generation Derived from Water Dissociation Under Supercontinuum Solar Light (25)

2020 ◽  
Vol MA2020-02 (61) ◽  
pp. 3105-3105
Author(s):  
Kenji Sakamaki ◽  
Yume Honda ◽  
Yumena Kobayashi ◽  
Rina Yoshida ◽  
Erika Hiruta ◽  
...  
Keyword(s):  
Hydrogen Generation ◽  
Solar Light ◽  
Water Dissociation

scholarly journals Synergistic Interfacial and Doping Engineering of Heterostructured NiCo(OH)x-CoyW as an Efficient Alkaline Hydrogen Evolution Electrocatalyst

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Ruopeng Li ◽  
Hao Xu ◽  
Peixia Yang ◽  
Dan Wang ◽  
Yun Li ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
High Efficiency ◽  
Low Voltage ◽  
Electrochemical Etching ◽  
Synergistic Effects ◽  
Release Kinetics ◽  
Water Electrolysis ◽  
Water Dissociation ◽  
Practical Applications ◽  
Environmentally Friendly Process

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.

scholarly journals Electrodeposition of Pt-Decorated Ni(OH)2/CeO2 Hybrid as Superior Bifunctional Electrocatalyst for Water Splitting

Research ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Huanhuan Liu ◽  
Zhenhua Yan ◽  
Xiang Chen ◽  
Jinhan Li ◽  
Le Zhang ◽  
...  
Keyword(s):  
Water Splitting ◽  
Cell Voltage ◽  
Water Electrolysis ◽  
Active Species ◽  
Water Dissociation ◽  
Electronic Interaction ◽  
Bifunctional Electrocatalyst ◽  
Highly Active ◽  
A Cell ◽  
Promising Application

The facile synthesis of highly active and stable bifunctional electrocatalysts to catalyze water splitting is attractive but challenging. Herein, we report the electrodeposition of Pt-decorated Ni(OH)2/CeO2 (PNC) hybrid as an efficient and robust bifunctional electrocatalyst. The graphite-supported PNC catalyst delivers superior hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) activities over the benchmark Pt/C and RuO2, respectively. For overall water electrolysis, the PNC hybrid only requires a cell voltage of 1.45 V at 10 mA cm−2 and sustains over 85 h at 1000 mA cm−2. The remarkable HER/OER performances are attributed to the superhydrophilicity and multiple effects of PNC, in which Ni(OH)2 and CeO2 accelerate HER on Pt due to promoted water dissociation and strong electronic interaction, while the electron-pulling Ce cations facilitate the generation of high-valence Ni OER-active species. These results suggest the promising application of PNC for H2 production from water electrolysis.

scholarly journals Electrochemically Induced In-Situ Generated Co(OH)2 Nanoplates to Promote the Volmer Process Toward Efficient Alkaline Hydrogen Evolution Reaction

2020 ◽  
Author(s):  
Hong Liu ◽  
Jian-Jun Wang ◽  
Li-Wen Jiang ◽  
Yuan Huang ◽  
Bing Bing Chen ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Active Sites ◽  
Water Electrolysis ◽  
Water Dissociation ◽  
Alkaline Water Electrolysis ◽  
Additional Water ◽  
Dissociation Step ◽  
Insight Into

<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>

Boosting eco-friendly hydrogen generation by urea-assisted water electrolysis using spinel M2GeO4 (M = Fe, Co) as an active electrocatalyst

2021 ◽  
Author(s):  
Hyeonuk Choi ◽  
Surendran Subramani ◽  
Dohun Kim ◽  
Yoongu Lim ◽  
Jeahyoung Lim ◽  
...  
Keyword(s):  
Hydrogen Production ◽  
Hydrothermal Method ◽  
Hydrogen Generation ◽  
Water Electrolysis ◽  
One Pot ◽  
Spinel Structures ◽  
Bimetallic Oxides

To enhance the efficiency of hydrogen production, bimetallic oxides with spinel structures, M2GeO4 (M = Fe, Co), were synthesized via a facile one-pot hydrothermal method and were used as electrocatalysts...

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