Photo- and Electrocatalytic Dual-Layer Cathode Facilitating Zn Peroxide Chemistry in Near-Neutral Zn-Air Batteries.

J Am Chem Soc

College of Energy Material and Chemistry, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.

Published: March 2025

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.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jacs.4c14009DOI Listing

Publication Analysis

Top Keywords

outer photocatalyst
12
photocatalyst layer
12
o/zno conversion
8
voltage hysteresis
8
layer exposed
8
inner cnt
8
cnt layer
8
layer
6
photo- electrocatalytic
4
electrocatalytic dual-layer
4

Similar Publications

Photo- and Electrocatalytic Dual-Layer Cathode Facilitating Zn Peroxide Chemistry in Near-Neutral Zn-Air Batteries.

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 PDF

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 PDF

MOF-Based Dual-Layer Pickering Emulsion: Molecular-Level Gating of Water Delivery at Water-Oil Interface for Efficient Photocatalytic Hydrogenation Using HO as a Hydrogen Source.

Angew 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.

Article Synopsis
  • The biphasic system offers a unique approach for complex catalytic processes by combining photocatalysis with hydrogenation, highlighting both its potential and accompanying challenges.
  • Researchers utilized metal-organic frameworks (MOFs) and CdS nanorods to create a dual-layer Pickering emulsion that effectively separates the photocatalytic hydrogen evolution reaction (HER) in the aqueous phase from oil-soluble hydrogenation.
  • This innovative setup achieved an impressive hydrogenation yield of 187.37 mmol·g-1·h-1 and a high apparent quantum yield of 43.24%, demonstrating significant improvements over traditional methods and providing valuable insights for future tandem catalytic processes.
View Article and Find Full Text PDF

Bioinspired catalytic pocket promotes CO-to-ethanol photoconversion on colloidal quantum wells.

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 PDF

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.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!