In this study, high quality Magnéli phase TiO bulks with electrical conductivity up to 961.5 S cm were successfully prepared by spark plasma sintering (SPS) and then served as electrode materials for electrochemical oxidation of azo dye methyl orange (MO). The influences of current density and initial dye concentration on the removal rates of MO and chemical oxygen demand (COD) were studied. Removal of MO and COD exhibited an increase with increasing current density and decreasing initial concentration of MO. Complete removal of MO was realized within a short time under all experimental conditions. The removal rate of COD reached 91.7% when current density was 10 mA cm and initial dye concentration was 100 mg L. In addition, the electrochemical oxidation rate could be described through a pseudo-first-order kinetic constant k, and the obtained experimental results could be well fitted with a proposed kinetic model in all the examined conditions. Possible degradation mechanisms for electrochemical oxidation of MO by TiO electrode were proposed on the basis of intermediate products analysis. Tests were also conducted with other commercial electrodes for comparison, including commercial graphite, stainless-steel and dimension stable anode (DSA) electrodes. The results showed that TiO anode exhibited the fastest electrochemical oxidation rates than those of the other electrodes. This study provides a feasible method for realizing high efficiency of electrochemical oxidation degradation by TiO electrode.
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http://dx.doi.org/10.1016/j.chemosphere.2019.125084 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Research Center for Energy and Environmental Materials, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.
Unveiling the key influencing factors towards electrode/electrolyte interface control is a long-standing challenge for a better understanding of microscopic electrode kinetics, which is indispensable to building up guiding principles for designer electrocatalysts with desirable functionality. Herein, we exemplify the oxygen evolution reaction (OER) via water molecule oxidation with the iridium dioxide electrocatalyst and uncovered the significant mismatching effect of pH between local electrode surface and bulk electrolyte: the intrinsic OER activity under acidic or near-neutral condition was deciphered to be identical by adjusting this pH mismatching. This result indicates that the local pH effect at the electrified solid-liquid interface plays the main role in the "fake" OER performance.
View Article and Find Full Text PDFChemistry
January 2025
National Tsing Hua University, Department of Chemical Engineering, 101, Sec 2, Kuang-Fu Rd., 300, Hsinchu, TAIWAN.
This study focuses on enhancing the water oxidation reaction (WOR) efficacy of dinuclear cobalt complex catalysts from both kinetic (turnover frequency, TOF) and thermodynamic (overpotential, η) perspectives. For this purpose, we synthesized six dinuclear cobalt complexes 1-6 comprising non-innocent ligands with different electronically active substituents (-OMe (1), -Me (2), -H (3), -F (4), -Cl (5), and -CN (6)). The electronic effects on the electrochemical WOR under neutral, acidic, and alkaline conditions were investigated experimentally and computationally.
View Article and Find Full Text PDFSmall
January 2025
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, No. 174 Shazheng Road, Chongqing, 400044, China.
Direct electrochemical detection of miRNA biomarkers in tumor tissue interstitial fluid (TIF) holds great promise for adjuvant therapy for tumors in the perioperative period, yet is limited by background interference and weak signal. Herein, a wash-free and separation-free miRNA biosensor based on photoexcited electro-driven reactive oxygen channeling analysis (LEOCA) is developed to solve the high-fidelity detection in physiological samples. In the presence of miRNA, nanoacceptors (ultrasmall-size polydopamine, uPDA) are responsively assembled on the surface of nanodonors (zirconium metal-organic framework, ZrMOF) to form core-satellite aggregates.
View Article and Find Full Text PDFSci Rep
January 2025
Chemistry Department, Faculty of Science, Cairo University, Giza, 12613, Egypt.
Azithromycin (AM) is one of the prescribed drugs in pandemic medication treatment which has paid great attention. We developed in this study a simply modified carbon paste electrode (CPE) to detect AM using poly-threonine (PT). PT or similar polymers are used as carriers to enhance the delivery and effectiveness of AM.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Energy Engineering, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea.
Organic anode materials have garnered attention for use in rechargeable Li-ion batteries (LIBs) owing to their lightweight, cost-effectiveness, and tunable properties. However, challenges such as high electrolyte solubility and limited conductivity, restrict their use in full-cell LIBs. Here, we report the use of highly crystalline Cl-substituted contorted hexabenzocoronene (Cl-cHBC) as an efficient organic anode for full-cell LIBs.
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