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Designing a low-cost, high-efficiency and robust doped-carbon-based oxygen reduction reaction electrocatalyst for large-scale implementations of fuel cells is highly desirable but challenging. In this work, we report a new type of hollow FeO with oxygen vacancy incorporating on mesoporous carbon prepared by pyrolyzing mesoporous carbon enriched with oxygen-containing functional groups, in combination with ferric acetylacetonate. The catalysts possess high specific surface area with predominantly mesoporous architecture and ultrahigh nitrogen content (up to 7.47 wt%). Benefiting from the integration of abundant active nitrogen and Fe-N species, and synergistic effect between FeO nanoparticles cooperated with oxygen vacancy and N-doped carbon, the half-wave potential of the preparing hybrid catalyst is 30 mV more positive than that of the commercial Pt/C catalyst in alkaline medium, and exhibits a high selectivity (4 e process), and outstanding long-term stability. More importantly, the C-FePPDA-900 catalyst displays a high power density (106 mW cm) and specific capacity of 724 mAh g when it is used as an air cathode catalyst in a specifically assembling Zn-air cell, superior to those of most reported catalysts.
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http://dx.doi.org/10.1016/j.jcis.2020.02.013 | DOI Listing |
Int J Radiat Biol
September 2025
Department of Geography, Nara Women's University, Nara, Japan.
Purpose: The number of oxygen vacancies in quartz measured by electron spin resonance (ESR) as the intensity of the E' center has been used to investigate the provenance of the sediments and has been found to be a good proxy in discussing the direction and intensity of the wind system in the past. While its temporal variations have been examined using marine sediments. The present study aimed to show that terrestrial sediments are also useful for such studies on climate change when it is continuous.
View Article and Find Full Text PDFLangmuir
September 2025
Key Laboratory of Functional Molecular Solids (Ministry of Education), College of Chemistry and Materials Science, Anhui Key Laboratory of Biomedical Materials and Chemical Measurement, Anhui Normal University, Wuhu 241000, China.
The sluggish kinetics and diffusion of lithium polysulfide (LiPS) intermediates lead to the decline in the capacity and rate of high-energy lithium-sulfur (Li-S) batteries. Integrating adsorbents and electrocatalysts into the Li-S system is an effective strategy for suppressing the polysulfide shuttle and enhancing the redox kinetics of sulfur species. The disordered structure of the electrocatalysts exhibits significantly enhanced catalytic activity.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Biomedical Engineering, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Electrochemical CO reduction reaction (CORR) has emerged as a key negative-emission technology, yet its industrial adoption hinges on cathode catalysts that deliver high selectivity and production rates at low cost. Herein, we reported a facile hydrothermal route to synthesize different scales of ZnOHF ultrathin nanowires with hybridized ZnO/ZnOHF heterointerfaces, where the 40 nm variant (NW-ZnOHF) showed a high FE of 93 % and a of -17.2 mA/cm at -1.
View Article and Find Full Text PDFAdv Mater
September 2025
Key Lab of Artificial Micro- and Nano-Structures of Ministry of Education of China, School of Physics and Technology, Wuhan University, Wuhan, 430072, China.
Sequential deposition technique is widely used to fabricate perovskite films with large grain size in perovskite solar cells (PSCs). Residual lead halide (PbI) in the perovskite film tends to be decomposed into metallic lead (Pb) under long-term heating or light soaking. Here, a chiral levetiracetam (LEV) dopant containing α-amide and pyrrolidone groups is introduced into the PbI precursor solution.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (O) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which O actively participates in O-O bond formation and is continuously refilled by water-derived species.
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