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Bifunctional oxygen electrocatalysts play a crucial role in the performance of rechargeable zinc-air batteries (ZABs), directly impacting key parameters such as capacity, round-trip efficiency, and durability. The ideal electrocatalysts for ZAB air electrodes must exhibit high catalytic activity for both oxygen reduction and oxygen evolution reactions in alkaline medium. This study presents a potassium-ion doping strategy to engineer the electron and defect structures of the perovskite oxide main phase, promoting phase separation to form a nanocomposite consisting of a perovskite phase and a secondary phase with an intergrowth structure. The resulting nanocomposite catalyst exhibits increased concentrations of Co and oxygen vacancies, enhanced hydrophilicity, and improved adsorption of oxygen intermediates. As a result, the catalyst with the optimized composition demonstrates exceptional bifunctional activity and superior durability, leading to extended cycling stability and improved energy conversion efficiency in ZABs. Notably, it achieves a 42% increase in power density compared to the potassium-free pristine catalyst, a reduced voltage gap (ΔE = 0.83 V), and an extended cycle life of over 250 h. This work introduces a novel design paradigm for advanced metal-air battery catalysts through potassium-promoted defect-engineered heterostructure manipulation of perovskite oxides.
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http://dx.doi.org/10.1002/smll.202502595 | DOI Listing |
Dalton Trans
September 2025
University of Belgrade, Faculty of Physical Chemistry, Studentski trg 12-16, 11158 Belgrade, Serbia.
Developing efficient, low-cost catalysts for oxygen reduction and evolution reactions (ORR and OER) is key to advancing metal-air batteries and regenerative fuel cells. In this study, nitrogen-doped binary metal (Mn and Ni) oxides (N-BMOs) and Pt-decorated N-BMOs were synthesised using three methods and tested as ORR and OER catalysts in alkaline media. Their physicochemical properties were characterised by XRD, N-sorption, TEM, and XPS, while their electrochemical performance was evaluated using voltammetry and impedance spectroscopy.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
State Key Laboratory of Heavy Oil Processing, China University of Petroleum (Beijing), Changping, 102249, China. Electronic address:
Carbon-based catalysts with free-standing structure are essential for rechargeable zinc-air battery as electrodes, which can avoid the side effects brought by organic binder. However, the current preparation methods still can be improved for faster preparation process and morphology control. In this study, we reported a fabrication strategy of self-standing carbon catalyst loaded with CoFe nanoparticles and carbon nanotube as air electrodes for liquid rechargeable zinc-air battery.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, National Center for International Research on Catalytic Technology, School of Chemistry and Materials Science, Heilongjiang University, Harbin 150080, P. R. China.
Seawater electrolysis offers a sustainable pathway for green hydrogen production, but chloride-induced side reactions, particularly chlorine evolution (ClER), limit the stability and efficiency of catalysts. Based on an interface-engineering strategy, a bifunctional CoP-MXene electrocatalyst was designed and fabricated, in which electrons are transferred from the Ti sites of the MXene support to the adjacent Co active centers of CoP. This directional electron donation modulates the Co electronic structure, generating electron-rich Co sites that effectively suppress Cl adsorption via electronic repulsion while preserving the OH reaction pathways through favorable proton-electron coupling.
View Article and Find Full Text PDFSmall
September 2025
State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu, 610065, China.
Nucleophilic substitution reaction (SR) plays a crucial role in traditional organic chemistry, and its extension into two dimensional (2D) materials has recently created a series of functional materials and advanced applications. However, the traditional SR process is usually indiscriminately copied into existing 2D reaction systems, which tremendously restricts the development of special 2D functional materials and sophisticated applications. In this work, a brand-new spin-active polarons-induced SR process in typical 2D fluorographene (FG) is proposed, where nucleophiles preferentially attack particular oxygen groups for functional grafting, simultaneously inducing the generation of spin-active polarons and subsequently rapid defluorination on the FG nanosheet.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Institute of Materials Intelligent Technology, Liaoning Academy of Materials, Shenyang 110004, China.
Axial ligand engineering is a promising strategy to enhance the performance of single-atom catalysts (SACs) in electrocatalysis. However, a single non-metallic axial coordination atom linked to monolayer SACs (MSACs) often exhibits insufficient stability. In this work, we designed a series of bilayer SACs (BSACs) with vertically stacked FeN and MN (M = Sc-Zn) layers bridged by axial non-metallic atoms (C, N, O, P, S, and Se).
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