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Modulating the Oxygen Evolution Reaction of Single-Crystal Cobalt Carbonate Hydroxide via Surface Fe Doping and Facet Dependence.
J Phys Chem Lett
January 2025
Graphene Composite Research Center, College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, P. R. China.
The oxygen evolution reaction (OER) is a critical half-reaction in water splitting and metal-air cells. The sensitivity of the OER to the composition and structure of the electrocatalyst presents a significant challenge in elucidating the structure-property relationship. In this study, highly stable single-crystal cobalt carbonate hydroxide [Co(OH)CO, CoCH] was used as a model to investigate the correlations among structure, composition, and reactivity.
View Article and Find Full Text PDFUnraveling the Role of Alkali on Cobalt Catalyst Performance in Ethanol Steam Reforming by Operando DRIFT Studies and DFT Modeling.
ACS Appl Mater Interfaces
January 2025
Faculty of Chemistry, Jagiellonian University in Krakow, Gronostajowa 2, 30-387 Krakow, Poland.
Hydrogen, a sustainable and environmentally friendly fuel, can be obtained through the ethanol steam reforming (ESR) process. The most promising catalysts for this process are those based on non-noble metals such as cobalt. The activity, selectivity, and stability of these catalysts strongly depend on the presence of alkali dopants.
View Article and Find Full Text PDFD-Histidine modulated chiral metal-organic frameworks for discriminating 3,4-Dihydroxyphenylalanine enantiomers based on a chemiluminescence quenching mode.
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.
View Article and Find Full Text PDFConjugated phthalocyanine-based framework as artificial SEI for over 400 Wh kg lithium-metal battery.
Natl Sci Rev
February 2025
School of Chemistry, South China Normal University, Guangzhou 510006, China.
High-voltage lithium-metal batteries (HVLMBs) are appealing candidates for next-generation high-energy rechargeable batteries, but their practical applications are still limited by the severe capacity degradation, attributed to the poor interfacial stability and compatibility between the electrode and the electrolyte. In this work, a 2D conjugated phthalocyanine framework (CPF) containing single atoms (SAs) of cobalt (CoSAs-CPF) is developed as a novel artificial solid-electrolyte interphase (SEI) in which a large amount of charge is transferred to the CPF skeleton due to the Lewis acid activity of the Co metal sites and the strong electron-absorbing property of the cyano group (-CN), greatly enhancing the adsorption of the Li and regulating the Li distribution toward dendrite-free LMBs, which are superior to most of the reported SEI membranes. As a result, the Li||Li symmetrical cell with CoSAs-CPF-modified Li anodes (CoSAs-CPF@Li) exhibits a low polarization with an area capacity of 1.
View Article and Find Full Text PDFCobalt-Zinc carbonaceous yolk-shell reactor enhances electron transfer in non-radical pathways: Electric potential concentration effect via bimetallic synergy.
J 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.
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