Hydrogen economy has emerged as a promising alternative to the current hydrocarbon economy. It involves harvesting renewable energy to split water into hydrogen and oxygen and then further utilising clean hydrogen fuel for various applications. The rational exploration of advanced non-precious metal bifunctional electrocatalysts for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is critical for efficient water splitting. Herein, an ultralow Ru-modified cobalt metal-organic framework (CoRu-MOF/NF) two-dimensional nanosheet array bifunctional catalyst was fabricated through a strategy under mild experimental conditions. The obtained CoRu-MOF/NF exhibited excellent bifunctional electrocatalytic activity and stability in alkaline media, with low overpotentials of 37 and 181 mV and significant durability for more than 95 and 110 h toward the HER and OER at 10 mA cm, respectively. The experimental results showed that the two-dimensional nanoarray structure had a large specific surface area and abundant exposed active sites. Additionally, ultralow Ru modification optimized the electronic structure and improved the conductivity of the cobalt metal-organic frameworks, thereby reducing the energy barrier of the rate-limiting step and accelerating the water splitting reaction.
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Anal Chim Acta
February 2025
Key Laboratory of Luminescence Analysis and Molecular Sensing (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing, 400715, China. Electronic address:
Background: Drug enantiomers often display distinguishable or even opposite pharmacological and toxicologic activities. Therefore it is of great necessity to discriminate enantiomers for guaranteeing safetyness and effectiveness of chiral drugs. Facile chiral discrimination has long been a noticeable challenge because of the minimal differences in physicochemical properties of enantiomers.
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January 2025
School of Integrated Technology, College of Engineering, Yonsei University, 85 Songdogwahak-ro, Yeonsu-gu, Incheon, 21983, Republic of Korea.
Poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) based electrolyte is a promising alternative to liquid electrolytes in lithium metal batteries. However, its commercial application is limited by high crystallinity and low Li ion conductivity. In this study, we synthesized a fluorinated Li-based metal-organic framework (Li-MOF-F) and used it as a filler to address these limitations.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
School of Environment and Energy, South China University of Technology, Guangzhou 510006 China; Guangdong Plant Fiber High-Valued Cleaning Utilization Engineering Technology Research Center, Guangzhou 510640 China. Electronic address:
Bimetallic catalysts have notable advantages in the field of persulfate activation owing to their intermetallic synergy. However, studies on stimulating the potential concentration effect through intermetallic coordination to enhance the electron transfer efficiency are limited. In this study, a cobalt (Co) and zinc (Zn) bimetallic yolk-shell structured high-efficiency peroxymonosulfate (PMS) catalyst (Z67@8-HCNF) was prepared by the derivatization of metal-organic backbone materials and was found to produce significant synergistic interactions between Co and Zn metals, which could be utilized to trigger the potential concentration effect to enhance the intermolecular electron transfer efficiency and achieve efficient PMS activation.
View Article and Find Full Text PDFChemSusChem
December 2024
Department of Chemistry, Chungnam National University, Daejeon, 34134, Republic of Korea.
Catalyst design plays a critical role in ensuring sustainable and effective energy conversion. Electrocatalytic materials need to be able to control active sites and introduce defects in both acidic and alkaline electrolytes. Furthermore, producing efficient catalysts with a distinct surface structure advances our comprehension of the mechanism.
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January 2025
Leiden University: Universiteit Leiden, Leiden Institute of Chemistry, Einsteinweg 55, Room number EE4.19, 2333 CC, Leiden, NETHERLANDS, KINGDOM OF THE.
Electrocatalysis in metal-organic frameworks is an interplay between the diffusion of charges, the intrinsic catalytic rate, and the mass-transport of reactants through the pores. Here a systematic study is carried out to investigate the role of the electrolyte nature and concentration on the oxygen reduction reaction (ORR) with the PCN-224(Co) MOF in aqueous electrolyte. It was found that the ORR activity is slightly influenced by the nature of the ions in solution, providing that the ionic strength is high enough to minimize the resistivity during the measurement.
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