Green hydrogen produced by alkaline electrolysis is a promising solution to address the world's increasing energy demand while mitigating greenhouse gas emissions. However, the efficient and cost-effective production of green hydrogen via alkaline electrolysis requires improvements. This paper presents an in situ activation process that simplifies the alkaline electrolysis technology while enhancing the catalytic activity of electrodes for the hydrogen evolution reaction. The aim of this research is to enhance the energy efficiency of alkaline electrolysis and decrease the energy consumption for hydrogen production. To achieve this goal, ionic activators comprising Ni, Zn, and Mo were incorporated into the standard electrolyte solution. Our results demonstrate that the anticipated improvement in the catalytic activity of the d-metal combination, surpassing even that of precious metals, has been successfully attained. As a result, a 20% reduction in energy consumption (REC) for the hydrogen produced has been observed. The catalytic activity of the added activators for the hydrogen evolution reaction was discussed by analyzing the mechanism of the reaction via Tafel analysis and EIS techniques. These findings offer a promising approach to improve alkaline electrolysis and enhance the production of green hydrogen.
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http://dx.doi.org/10.3390/ma16155268 | DOI Listing |
ACS Nano
January 2025
College of Chemistry Chemical Engineering and Materials Science, Shandong Normal University, Jinan, Shandong 250014, China.
Coastal/offshore renewable energy sources combined with seawater splitting offer an attractive means for large-scale H electrosynthesis in the future. However, designing anodes proves rather challenging, as surface chlorine chemistry must be blocked, particularly at high current densities (). Additionally, waste seawater with increased salinity produced after long-term electrolysis would impair the whole process sustainability.
View Article and Find Full Text PDFNanoscale
January 2025
Department of Chemistry, Material Science Lab, Annamalai University, Annamalai Nagar, Tamil Nadu 608002, India.
The urgent need to address escalating environmental pollution and energy management challenges has underscored the importance of developing efficient, cost-effective, and multifunctional electrocatalysts. To address these issues, we developed an eco-friendly, cost-effective, and multifunctional electrocatalyst a solvothermal synthesis approach. Due to the merits of the ideal synthesis procedure, the FeCoHS@NF electrocatalyst exhibited multifunctional activities, like OER, HER, OWS, UOR, OUS, and overall alkaline seawater splitting, with required potentials of 1.
View Article and Find Full Text PDFJACS Au
December 2024
Shanghai Key Laboratory for R&D and Application of Metallic Functional Materials, Institute of New Energy for Vehicles, School of Materials Science and Engineering, Tongji University, 201804, Shanghai, China.
For the aim of achieving the carbon-free energy scenario, green hydrogen (H) with non-CO emission and high energy density is regarded as a potential alternative to traditional fossil fuels. Over the last decades, significant breakthroughs have been realized on the alkaline hydrogen evolution reaction (HER), which is a fundamental advancement and efficient process to generate high-purity H in the laboratory. Based on this, the development of the practical industry-oriented anion exchange membrane water electrolyzer (AEMWE) is on the rise, showing competitiveness with the incumbent megawatt-scale H production technologies.
View Article and Find Full Text PDFMembranes (Basel)
December 2024
Department of Green Chemical Engineering, College of Engineering, Sangmyung University, Cheonan 31066, Republic of Korea.
This study examines the effect of the structural characteristics of anion-conducting monomers within pore-filling anion exchange membranes on the performance and durability of anion exchange membrane water electrolysis. Analysis reveals that acrylamide- and acrylate-based membranes show optimal performance without methyl groups, with acrylamide-based membranes outperforming their acrylate counterparts in current density, particularly at 1.8 V.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
City University of Hong Kong, Department of Chemistry, Tat Chee Avenue, 000000, Kowloon, HONG KONG.
Electrocatalytic CO2 reduction (CO2R) to multi-carbon (C2+) products in strong acid presents a promising approach to mitigate the CO2 loss commonly encountered in alkaline and neutral systems. However, this process often suffers from low selectivity for C2+ products due to the competing C1 (e.g.
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