The microbial separator (MS) was promising alternative of ion exchange membrane for biocathode microbial electrochemical system (MES). Four microbial separators developed from porous matrixes were equipped in biocathode MESs. The power generation of MESs responded to cross-separator transfer characters of ions, dissolved oxygen (DO) and chemical oxygen demand (COD). The MES with carbon felt (CF) obtained 31% higher maximum power density at 70 ± 3 mW m and 51% higher current density at 271 ± 21 mA m than those of cation exchange membrane (CEM) separator. All MSs showed higher ionic conductivity than CEM. However, the power variation was mainly due to cathodic equilibrium potential changes rather than internal resistance. The power density demonstrated negative correlation with mass transfer coefficients of DO and COD. The cross-separator transfer of COD caused cathode variation and was identified as the primary parameter for further optimization of MES with microbial separators.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.biortech.2020.123478 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Functional Materials and Electrochemistry Lab, Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal 721302, India.
The rational design and synthesis of bifunctionally active and durable oxygen electrocatalysts have garnered significant attention for electrochemical energy conversion and storage. Intermetallic nanostructures are particularly promising for these applications due to their unique catalytic properties and exceptional durability. In this study, we present a fascinating synthetic approach for the direct synthesis of a bifunctional oxygen electrocatalyst based on nitrogen-doped carbon-encapsulated ordered PdFe (o-PdFe@NC) intermetallic, using a cyano-bridged bimetallic single-source precursor tailored for aqueous rechargeable zinc-air batteries (ZABs).
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Département de chimie, Université de Sherbrooke, Sherbrooke, Québec J1K 2R1, Canada.
Two new nonfused ring nonfullerene electron acceptors, NFAs, (dicarbazolyl)bis(2-(3-oxo-2,3-dihydro-1-inden-1-ylidene)malononitrile) () and -(2-(5,6-fluoro-3-oxo-2,3-dihydro-1-inden-1-ylidene)malononitrile) (), thus exhibiting an A-D-A motif, were synthesized and characterized. As thin films, they exhibit the lowest energy absorption signature near 540 nm, extending down to ∼700 nm. This band is due to an intramolecular charge transfer process from the (nonfused dicarbazoyl; ) moiety to the malononitrile-based units () based on density functional theory calculations (DFT), which are also corroborated by time-dependent DFT (TDDFT) computations.
View Article and Find Full Text PDFJ Chem Phys
January 2025
School of Physics, Shandong University, Jinan 250100, China.
We apply the trajectory formulation to analyze the anomalous dynamics of cold atoms in an optical lattice. The phase space probability density function of cold atoms, their dynamics, and the mechanism of dynamic evolution from an initial Gaussian distribution to a power-law distribution are analyzed. The results of the trajectory formulation are in good agreement with the previously reported experimental results for the exponent of position variance for a long time and the position-momentum correlation.
View Article and Find Full Text PDFSmall
January 2025
Centre for Nanotechnology, Indian Institute of Technology Roorkee, Roorkee, 247667, India.
To rival commercial organic electrolytes, it is important to focus on safe, cheap aqueous electrolytes with lower salt concentration (≈5.0 m) and a wider electrochemical stable potential window (ESPW). This study reports the facile synthesis of porphyrin-based covalent organic polymers (PTZ-COP, CBZ-COP, and TPA-COP) through a one-pot aromatic electrophilic polycondensation reaction between pyrrole and monomeric aldehydes (PTZ-CHO, CBZ-CHO and TPA-CHO).
View Article and Find Full Text PDFSmall
January 2025
Key Laboratory of Colloid and Interface Chemistry of the Ministry of Education of the P. R. China, Shandong University, Jinan, 250100, P. R. China.
The dual-site electrocatalysts formed by metal single atoms combines with metal nanoparticles represent a promising strategy to enhance both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) performance. Herein, defect engineering is applied to dual-site ORR and OER electrocatalysts. Its design, synthesis, structural properties, and catalytic performance experimentally and theoretically are insightfully studied for the single-atomic Fe─N and the adjacent FeCo nanoalloy (FeCo) as dual-site loading on nitrogen-doped graphene aerogel (Fe─N/FeCo@NGA).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!