Rechargeable zinc-air batteries (ZABs) using near-neutral aqueous electrolytes are gaining significant attention due to their high energy density, low cost, high safety, and the excellent reversibility of the zinc (Zn) anode in mild electrolytes. However, the sluggish O/ZnO conversion in the carbon-based cathodes of these batteries leads to a large voltage hysteresis (>600 mV) between charge and discharge. Metal- or metal oxide-based electrocatalysts are rarely used to reduce the overpotentials of this conversion because their presence may trigger undesirable HO-participated oxygen reduction/evolution reactions, disrupting the pH balance of the electrolyte. Here, we propose a dual-layer catalytic cathode comprising an outer photocatalyst layer (exposed to air) of gold (Au) nanoparticles (NPs) decorated tungsten oxide (Au@WO) loaded on carbon paper, and an inner electrocatalyst layer (exposed to the electrolyte) based on carbon nanotube (CNT). The hydrophobic inner CNT layer not only provides numerous active sites and ample accommodation for O/ZnO conversion but also prevents the electrolyte from contacting the outer photocatalyst layer. Under light, the outer photocatalyst layer effectively separates photogenerated electron-hole pairs, which are then transferred to the inner CNT layer, reducing the overpotential of the O/ZnO electrochemical conversion. As a result, the near-neutral ZAB demonstrates high stability at 0.1 mA cm; with a very small voltage hysteresis (<150 mV), significantly improving energy efficiency.
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http://dx.doi.org/10.1021/jacs.4c14009 | DOI Listing |
J Am Chem Soc
March 2025
College of Energy Material and Chemistry, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.
Rechargeable zinc-air batteries (ZABs) using near-neutral aqueous electrolytes are gaining significant attention due to their high energy density, low cost, high safety, and the excellent reversibility of the zinc (Zn) anode in mild electrolytes. However, the sluggish O/ZnO conversion in the carbon-based cathodes of these batteries leads to a large voltage hysteresis (>600 mV) between charge and discharge. Metal- or metal oxide-based electrocatalysts are rarely used to reduce the overpotentials of this conversion because their presence may trigger undesirable HO-participated oxygen reduction/evolution reactions, disrupting the pH balance of the electrolyte.
View Article and Find Full Text PDFACS Appl Nano Mater
January 2025
Department of Physics, University of Cagliari, Complesso Universitario di Monserrato S.P. Monserrato-Sestu Km 0, 700 09042 Monserrato (CA), Italy.
Dual-functional photocatalysts help to maximize resource utilization in water remediation, but often they are visible-light-inactive, toxic, and cost-intensive. Herein, a type-II heterojunction visible-light-active photocatalyst is reported for tandem degradation of Rhodamine B and generation of H. A Rhodamine B degradation rate of 2.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
Institute for New Energy Materials and Low Carbon Technologies, School of Materials Science & Engineering, Tianjin University of Technology, Tianjin, 300384, P. R. China.
Sci Adv
November 2024
School of Materials Science and Engineering, School of Chemistry and Chemical Engineering, Beijing Key Laboratory of Construction-Tailorable Advanced Functional Materials and Green Applications, Experimental Center of Advanced Materials, Beijing Institute of Technology, Beijing 100081, China.
Sluggish surface reaction is a critical factor that strongly governs the efficiency of photocatalytic solar fuel production, particularly in CO-to-ethanol photoconversion. Here, inspired by the principles underlying enzyme catalytic proficiency and specificity, we report a biomimetic photocatalyst that affords superior CO-to-ethanol photoreduction efficiency (5.5 millimoles gram hour in average with 98.
View Article and Find Full Text PDFJ Colloid Interface Sci
February 2025
Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 610054, China.
The core-shell structure often exhibits unique properties, resulting in superior physical and chemical performance distinct from individual component in the field of photocatalysis. However, traditional prepared methods such as template synthesis and layer-by-layer self-assembly are relatively complex. Therefore, it is necessary to explore an efficient and expedient approach.
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