Dendritic zinc (Zn) electrodeposition presents a significant obstacle to the large-scale development of rechargeable zinc-ion batteries. To mitigate this challenge, various interfacial strategies have been employed. However, these approaches often involve the incorporation of foreign materials onto Zn anode surface, resulting in increased material costs and processing complexities, not to mention the compromised interface endurability due to structural and compositional heterogeneity. Realizing that Cu atoms typically exist as trace impurities in commercial Zn, a novel approach is demonstrated that leverages these Cu impurities to create a Cu-rich surface for effective modulation of Zn electrodeposition. By simply heating commercially available Zn foil with a naturally oxidized surface, not only the internal Cu atoms are thermally activated to become diffusible, their diffusion is also navigated toward the surface via oxygen attraction. The resulting Cu-rich surface effectively regulates Zn electrodeposition, comparable to conventional interfacial strategies, yet exhibits superior cycling durability. 3D in situ microscopy confirms that this Cu-rich surface enables dendrite-free, compact, and (101)-oriented Zn electrodeposition, contrasting with the traditional (002)-oriented dendrite-suppression mechanism. By transforming trace Cu impurity within Zn foil into a Cu-rich surface, this work demonstrates a straightforward, cost-effective and efficient method for controlling Zn electrodeposition.
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http://dx.doi.org/10.1002/adma.202420166 | DOI Listing |
Adv Mater
February 2025
Wenzhou Key Lab of Advanced Energy Storage and Conversion, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang, 325035, China.
Dendritic zinc (Zn) electrodeposition presents a significant obstacle to the large-scale development of rechargeable zinc-ion batteries. To mitigate this challenge, various interfacial strategies have been employed. However, these approaches often involve the incorporation of foreign materials onto Zn anode surface, resulting in increased material costs and processing complexities, not to mention the compromised interface endurability due to structural and compositional heterogeneity.
View Article and Find Full Text PDFBioabsorbable metallic alloys constitute a very challenging and innovative field, mainly aimed to develop the next generation of temporary medical implants. Degradation data, biological and tests are of major importance in particular for complex alloys, in which the individual element additions could enhance material performance and add functionalities. In this study, a novel Fe-Mn-Si-Cu alloy was carefully designed for vascular and blood-contact applications, and its microstructure, mechanical behavior, degradation behavior and biological performances were investigated accordingly.
View Article and Find Full Text PDFNat Commun
November 2024
Department of Chemistry, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai, China.
A bimetallic heterostructure has been shown effective to enhance the multi-carbon (C) product selectivity in CO electroreduction. Clarifying the interfacial structure under electrolysis and its decisive role in the pathway selection are crucial, yet challenging. Here, we conceive a well-defined Ag-Cu biphasic heterostructure to understand the interfacial structure-steered product selectivity: The Cu-rich interface prefers ethylene, while the dominant product switch to alcohols with an increasing Ag fraction, and finally to CO as Ag occupying the main surface.
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States.
ACS Appl Energy Mater
October 2024
Institute of Chemistry, University of Campinas, Campinas, SP 13083-862, Brazil.
Nitrate electroreduction reaction (NORR) to ammonia (NH) still faces fundamental and technological challenges. While Cu-based catalysts have been widely explored, their activity and stability relationship are still not fully understood. Here, we systematically monitored the dynamic alterations in the chemical and morphological characteristics of CuO nanocubes (NCs) during NORR in an alkaline electrolyte.
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