In this study, CoO@MoS is prepared as anodic catalytic material for microbial fuel cells (MFCs). As the mass fraction of MoS is 20%, the best performance of CoO@MoS composite catalytic material is achieved, and the addition of MoS enhances both the electrical conductivity and catalytic performance of the composite catalyst. Through the structural characterization of CoO@MoS composite catalytic material, nanorod-like CoO and lamellar MoS interweaved and stacked each other, and the agglomeration of CoO is weakened. Among the four groups of single-chamber MFCs constructed, the CoO@MoS-MFC shows the best power production performance with a maximum stable output voltage of to 539 mV and a maximum power density of up to 2221 mW/m. Additionally, the ammonia nitrogen removal rate of the MFCs loaded with catalysts is enhanced by about 10% compared with the blank carbon cloth MFC. Overall, the findings suggest that CoO@MoS composite catalysts can significantly improve the performance of MFCs, making them more effective for both energy production and wastewater treatment.
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http://dx.doi.org/10.1016/j.jenvman.2024.121966 | DOI Listing |
Phys Rev Lett
December 2024
Collaborative Innovation Center of Advanced Microstructures, National Laboratory of Solid State Microstructures, College of Engineering and Applied Sciences, Nanjing University, No. 22 Hankou Road, Nanjing, Jiangsu 210093, People's Republic of China.
Water electrolysis suffers from electron transfer barriers during oxygen evolution reactions, which are spin-related for magnetic materials. Here, the electron transfer at the Fe_{64}Ni_{36}-FeNiO_{x}H_{y} interface is effectively accelerated when the electrode is heated to trigger the Invar effect in Fe_{64}Ni_{36} Invar alloy, providing more unoccupied orbitals as electron transfer channels without pairing energy. As a result of thermally stimulated changes in electronic states, Fe_{64}Ni_{36}/FeNiO_{x}H_{y} achieved a cascaded oxidation of the catalytic center and water.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Physical & Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune, Maharashtra 411008, India.
This work aims to deal with the challenges associated with designing complementary bifunctional electrocatalysts and a separator/membrane that enables rechargeable zinc-air batteries (RZABs) with nearly solid-state operability. This solid-state RZAB was accomplished by integrating a bifunctional electrocatalyst based on Ru-RuO interface nanoparticles supported on nitrogen-doped (N-doped) graphene (Ru-RuO/NGr) and a dual-doped poly(acrylic acid) hydrogel (d-PAA) electrolyte soaked in KOH with sodium stannate additive. The catalyst shows enhanced activity and stability toward the two oxygen reactions, i.
View Article and Find Full Text PDFACS Nano
January 2025
College of Chemistry Chemical Engineering and Materials Science, Shandong Normal University, Jinan, Shandong 250014, China.
Coastal/offshore renewable energy sources combined with seawater splitting offer an attractive means for large-scale H electrosynthesis in the future. However, designing anodes proves rather challenging, as surface chlorine chemistry must be blocked, particularly at high current densities (). Additionally, waste seawater with increased salinity produced after long-term electrolysis would impair the whole process sustainability.
View Article and Find Full Text PDFAppl Biochem Biotechnol
January 2025
Department of Plant Sciences, Faculty of Biological Sciences, Quaid-I-Azam University Islamabad, Islamabad, 45320, Pakistan.
The current research was conducted to synthesize Parietaria alsinifolia-mediated iron oxide nanoparticles (P.A@FeONPs) using the green and eco-friendly protocol. The biosynthesized P.
View Article and Find Full Text PDFDalton Trans
January 2025
DICATECh, Politecnico di Bari, Bari, I-70125, Italy.
This systematic study delves into the synthesis and characterization of robust bi-functional aminopropyl-tagged periodic mesoporous organosilica with a high loading of small imidazolium bridges in its framework (PrNH@R-PMO-IL, ∼2 mmol g of IL). The materials proved to be a reliable and enduring support for the immobilization of Ru species, demonstrating strong performance and excellent selectivity in the -bromination of various derivatives of 2-phenylpyridine compounds and other heterocycles, showcasing its effectiveness and robust nature. The synthesized materials were thoroughly characterized to determine their structural properties, such as pore size distribution, loading of organic groups, and surface area, using various analytical techniques.
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