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To endow microbial fuel cells (MFCs) with low cost, long-term stability and high-power output, a novel cobalt-based cathode electrocatalyst (Nano-Co@NC) is synthesized from a polygonal metal-organic framework ZIF-67. After calcining the resultant ZIF-67, the as-synthesized Nano-Co@NC is characteristic of cobalt nanoparticles (Nano-Co) embedded in nitrogen-doped carbon (NC) that inherits the morphology of ZIF-67 with a large surface area. The Nano-Co particles that are highly dispersed and firmly fixed on NC not only ensure electrocatalytic activity of Nano-Co@NC toward the oxygen reduction reaction on the cathode, but also inhibit the growth of non-electrogenic bacteria on the anode. Consequently, the MFC using Nano-Co@NC as the cathode electrocatalyst demonstrates excellent performance, delivering a comparable initial power density and exhibiting far better durability than that using Pt/C (20 wt%) as the cathode electrocatalyst. The low cost and the excellent performance of Nano-Co@NC make it promising for MFCs to be used in practice.
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http://dx.doi.org/10.1039/d3cp02582a | DOI Listing |
ACS Electrochem
September 2025
Department of Chemistry, Molecular Sciences Research Hub, Imperial College London, White City Campus, Wood Lane, London W12 0BZ, United Kingdom.
The development of copper-catalyzed C-H functionalization processes is challenging due to the inefficiency of conventional chemical oxidants in regenerating the copper catalyst. This study details the development of a mediated electrosynthetic approach involving triple catalytic cycles in transient C-H functionalization to achieve efficient copper-catalyzed C-(sp)-H sulfonylation of benzylamines with sodium sulfinate salts. The triple catalytic system consists of a copper organometallic cycle for C-H functionalization, an aldehyde transient directing group (TDG) as an organocatalyst for imine formation, and a ferrocenium salt as an electrocatalyst.
View Article and Find Full Text PDFACS Electrochem
September 2025
Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.
The surface structure of an electrocatalyst plays a crucial role in determining the activity. As a model system, gold has been widely investigated as an electro-oxidation catalyst, although there has been much less research on the oxygen evolution reaction (OER) in the potential region of gold oxidation. Here, we combine voltammetric scanning electrochemical cell microscopy (SECCM) and electron backscatter diffraction (EBSD), at different spatial and angular resolutions, respectively, to correlate the local crystallographic structure of polycrystalline goldfocusing on grains close to (113), (011), (114), and (111) orientationswith the electrocatalytic behavior for the OER.
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 PDFSmall Methods
September 2025
School of Physics and Optoelectronics, South China University of Technology, Wushan Road 381, Guangzhou, 510640, China.
Magnetic-field enhancement of the oxygen evolution reaction (OER) represents a promising route toward more efficient alkaline water electrolyzers, yet its origin remains debated due to overlapping effects of mass transport and reaction kinetics. Here, we present a general experimental strategy that employs strong forced convection to suppress uncontrolled transport arising from natural diffusion and magnetohydrodynamic (MHD) flows. Using polycrystalline Au electrodes, we show that this approach resolves subtle OER variations under controlled flow and field conditions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, 130012, P.R. China.
Neutral aqueous Zn-air batteries (ZABs), while promising for extended lifespans and recyclability compared to alkaline systems, are hindered by sluggish kinetics that limit energy efficiency and power output. Here, we report an effective approach to construct a photo-assisted near-neutral ZAB based on a photo-responsive titanium silicalite-1 zeolite (TS-1). The incorporation of Ru active centers into the 3D porous architecture of TS@C (Ru@TS@C), which exhibits remarkably enhanced electronic conduction, creates interconnected conductive pathways.
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