Dimensionally stable anodes (DSA) were polarized at different constant potential values for several days in garden compost. After an initial lag period ranging from 1 to 10.5 days, the current increased fast and then stabilized for days. Current densities higher than 100 mA m(-2) and up to 385 mA m(-2) were obtained with the sole organic matter contained in compost as substrate. Control experiments performed with sterilized compost, oscillations of the current with the temperature, kinetics of the exponential phase of current increase and observations of the surface of electrodes by epifluorescence microscopy showed that the current was controlled by the colonization of the electrode surface by a biofilm which originated the indigenous flora of compost. Three individually addressed electrodes polarized at different potentials in the same reactor led to identical current evolutions on each electrode, which underlined the key role of the microbial flora of the compost in the discrepancy observed in the other experiments. Chronoamperometry revealed a promising technique to check natural environments for new electrochemically active microbial species.
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http://dx.doi.org/10.1016/j.biortech.2007.09.047 | DOI Listing |
Chem Sci
January 2025
Guangxi Key Laboratory of Electrochemical Energy Materials, School of Chemistry and Chemical Engineering, Guangxi University Nanning Guangxi 530004 China
Acentric crystalline materials are the cornerstone of numerous cutting-edge technologies and have been highly sought-after, but they are difficult to construct controllably. Herein, by introducing a new p-block element to break the symmetrical environment of the d transition metal in the centric matrix TiTeO, a novel acentric tellurite sulfate, namely Ti(TeO)(SO), was successfully constructed. In its structure, two types of p-block element-centered oxo-anionic groups, [TeO] and [SO], endow [TiO] with an out-of-center distortion along the local C[111] direction, which is rare in titanium oxides containing a lone-pair cation.
View Article and Find Full Text PDFChemistry
January 2025
Justus-Liebig Universität, Institut für Organische Chemie, Heinrich-Buff-Ring 17, 35392, Giessen, GERMANY.
Aryl diazenes, particularly azobenzenes (AB), represent a versatile class of compounds with significant historical and practical relevance, ranging from dyes to molecular machines, solar thermal and electrochemical storage. Their oxygen-substituted counterparts, azoxybenzenes (AOB), share structural similarities but have been less explored, especially in energy storage applications. This study investigates the redox properties of AOB, comparing them to AB, and evaluates their potential as redox-active materials for energy storage systems.
View Article and Find Full Text PDFJ Mater Chem B
January 2025
School of Chemistry and Materials Science, Ludong University, Key Laboratory of High Performance and Functional Polymer in the Universities of Shandong Province, Collaborative Innovation Center of Shandong Province for High Performance Fibers and Their Composites, Yantai 264025, China.
With the miniaturization, integration and intelligence of sweat electrochemical sensor technology, hydrogel flexible sensors have demonstrated immense potential in the field of real-time and non-invasive personal health monitoring. However, it remains a challenge to integrate excellent mechanical properties, self-healing properties, and electrochemical sensing capabilities into the preparation of hydrogel-based flexible sensors. The utilization of CBPG (cellulose nanocrystals (CNCs)@bovine serum albumin (BSA)@polyethyleneimine (PEI) glucose oxidase (GOD) nanomaterial) as both an enhancing phase and sensor probe within a hydrogel matrix, with poly(vinyl alcohol) (PVA) serving as the primary network constituent, has been proposed as a non-invasive technique for monitoring trace glucose levels in sweat.
View Article and Find Full Text PDFInorg Chem
January 2025
College of Material Science and Engineering, Guilin University of Technology, Guilin 541004, China.
Defining the active sites and further optimizing their activity are of great significance for enhancing the hydrogen evolution reaction (HER) performances, especially for inexpensive Ni-based catalysts doped with metals and nonmetal elements. This work reports the role of the incorporated molybdenum and sulfur in enhancing the HER activity of nickel. The prepared molybdenum and sulfur coincorporated Ni (NMS) electrocatalysts exhibit excellent HER performance, with an overpotential and Tafel slope of 77.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2020
State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249, P. R. China.
The lower limit of overpotential derived from the scaling relationship in the generally proposed adsorbate evolution mechanism (AEM) greatly hinders the oxygen evolution reaction (OER) activity in electrochemical energy conversion. The lattice oxygen mechanism tends to be triggered on oxygen-enriched surfaces under conditions; however, the required specific geometry and electronic structure need in-depth exploration. Here, tunable CoO is used as a model material, where the reconstruction of dominantly exposed (110) surface under reaction conditions is first presented using an thermodynamic approach.
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