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Metal-organic frameworks have been widely considered a potential alternative for noble metal catalysts for green hydrogen from seawater electrolysis, yet their performance is often limited by low activity and poor stability. Here, we propose a linker engineering strategy to optimize the phase composition of ultrathin Ni-MOF nanosheet arrays, aiming to enhance both activity and stability. We found that partial substitution of terephthalic acid (BDC) with electron-withdrawing tetrafluoroterephthalate (TFBDC) ligand alters the electronic structure and significantly promotes the formation of the catalytically active γ-NiOOH phase in Ni-TFBDC-2. This results in a 90 mV reduction in the overpotential for the oxygen evolution reaction at 50 mA cm, surpassing the performance of a state-of-the-art RuO catalyst, and is accompanied by an increased corrosion potential in seawater. Furthermore, the enrichment of the γ-NiOOH phase in Ni-TFBDC-2 effectively suppresses the passivation during urea oxidation reaction (UOR) in a seawater electrolyte, enabling the achievement of an industrially relevant current density of 0.8 A cm. Operando characterizations reveal that Ni-TFBDC-2 undergoes an electrooxidation process to form Ni species, which subsequently act as the active catalytic sites for the OER. Additionally, the urea-assisted natural seawater electrolyzer assembled with Ni-TFBDC-2 requires a low voltage of 1.76 V at 400 mA cm and demonstrates excellent durability over 170 h of continuous operation. This work offers a novel strategy to enrich the catalytically active phase in MOF-based electrocatalysts, aiming to achieve high activity and long-term stability during urea-assisted natural seawater electrolysis. It is noteworthy that different notable aspects, such as the durability of the materials after prolonged reaction, should be more thoroughly considered for practical applications on larger scales.
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http://dx.doi.org/10.1016/j.jcis.2025.138618 | DOI Listing |
J Colloid Interface Sci
September 2025
Center for Innovative Materials and Architectures, Ho Chi Minh City 700000, Viet Nam; Vietnam National University, Ho Chi Minh City 700000, Viet Nam. Electronic address:
Organic nucleophile-assisted natural seawater electrolysis has emerged as a promising strategy for green hydrogen production by significantly reducing energy consumption. Among Ni-based electrocatalysts, NiMoO has drawn attention for its activity in both oxygen evolution reaction (OER) and urea oxidation reaction (UOR). However, its practical application is hindered by severe surface passivation, particularly at industrial current densities (e.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2025
Center for Innovative Materials and Architectures, Ho Chi Minh City 700000, Viet Nam; Vietnam National University, Ho Chi Minh City 700000, Viet Nam. Electronic address:
Metal-organic frameworks have been widely considered a potential alternative for noble metal catalysts for green hydrogen from seawater electrolysis, yet their performance is often limited by low activity and poor stability. Here, we propose a linker engineering strategy to optimize the phase composition of ultrathin Ni-MOF nanosheet arrays, aiming to enhance both activity and stability. We found that partial substitution of terephthalic acid (BDC) with electron-withdrawing tetrafluoroterephthalate (TFBDC) ligand alters the electronic structure and significantly promotes the formation of the catalytically active γ-NiOOH phase in Ni-TFBDC-2.
View Article and Find Full Text PDFRSC Adv
July 2025
Institute of Materials Science, Vietnam Academy of Science and Technology Hanoi Vietnam
We present a facile synthesis method for a C-TiO-MoS-based photocatalytic nanocomposite designed for the efficient degradation of pollutant dyes, specifically methylene blue (MB) and rhodamine B (RhB). Few-layered MoS nanosheets were exfoliated from natural bulk MoS urea-assisted ball milling. These nanosheets were then mixed with TiO nanopowder and sodium deoxycholate (SDC) surfactant, followed by thermal annealing at 600 °C in argon (Ar) gas.
View Article and Find Full Text PDFChem Asian J
April 2025
Chemistry and Physics of Materials Unit, School of Advanced Materials (SAMat); JNCASR, Bengaluru, 560064, India.
Urea-assisted water electrolysis is a promising and energy-efficient alternative to electrochemical water splitting due to its low thermodynamic potential of 0.37 V, which is 860 mV less than that needed for water splitting (1.23 V).
View Article and Find Full Text PDFSmall
February 2025
College of Materials Science and Engineering, Sichuan University, Chengdu, 610065, P. R. China.
Nickel hydroxide (Ni(OH)) is considered to be one of the most promising electrocatalysts for urea oxidation reaction (UOR) under alkaline conditions due to its flexible structure, wide composition and abundant 3D electrons. However, its slow electrochemical reaction rate, high affinity for the reaction intermediate *COOH, easy exposure to low exponential crystal faces and limited metal active sites that seriously hinder the further improvement of UOR activities. Herein it is reported electrocatalyst composed of rich oxygen-vacancy (O) defects with amorphous SeO-covered Ni(OH) (O-SeO/Ni(OH)).
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