The electrochemical properties of cellulose dissolved in NaOH solution at a Au surface were investigated by cyclic voltammetry, FTIR spectroscopy, the electrochemical quartz crystal microbalance technique, and electrochemical impedance spectroscopy. The reaction products were characterized by SEM, TEM, and FTIR and NMR spectroscopy. The results imply that cellulose is irreversibly oxidized. Adsorption and desorption of hydroxide ions at the Au surface during potential cycling have an important catalytic role in the reaction (e.g., approach of cellulose to the electrode surface, electron transfer, adsorption/desorption of the reaction species at the electrode surface). Moreover, two types of cellulose derivatives were obtained as products. One is a water-soluble cellulose derivative in which some hydroxyl groups are oxidized to carboxylic groups. The other derivative is a water-insoluble hybrid material composed of cellulose and Au nanoparticles (≈4 nm). Furthermore, a reaction scheme of the electrocatalytic oxidation of cellulose at a gold electrode in a basic medium is proposed.
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http://dx.doi.org/10.1002/cssc.201402139 | DOI Listing |
Nat Commun
December 2024
Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology, School of Chemistry and Chemical Engineering, Northwestern Polytechnical University, Xi'an, Shaanxi, China.
Coordination complexes are promising candidates for powerful electrocatalytic oxygen evolution reaction but challenges remain in favoring the kinetics behaviors through local coordination regulation. Herein, by refining the synergy of carboxylate anions and multiconjugated benzimidazole ligands, we tailor a series of well-defined and stable coordination complexes with three-dimensional supramolecular/coordinated structures. The coordinated water as potential open coordination sites can directly become intermediates, while the metal center easily achieves re-coordination with water molecules in the pores to resist lattice oxygen dissolution.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
State Key Laboratory of Electrical Insulation and Power Equipment, Centre for Plasma Biomedicine, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.
Liquid fertilizers, particularly when integrated with precision irrigation systems, offer a more efficient and sustainable alternative to traditional solid nitrogen fertilizers. The industrial production of ammonium nitrate (NHNO) is environmentally detrimental due to its reliance on fossil fuels. This study introduces an innovative air-to-NOx-to-NHNO pathway for synthesizing liquid nitrogen fertilizer.
View Article and Find Full Text PDFChemistry
December 2024
Shaanxi Normal University, School of Chemistry and Chemical Engineering, Zhizhi Building 1206, 710119, Xi'an, CHINA.
Spinel oxides have attracted much attention in electrocatalytic water oxidation. Specially, the Mn-based spinel structures merits fundamental investigation, as Mn is involved in water oxidation in natural photosynthesis. Herein, Al-doped Mn3O4 spinel electrocatalyst was prepared for water oxidation.
View Article and Find Full Text PDFLangmuir
December 2024
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources and International Innovation Center for Forest Chemicals and Materials, Nanjing Forestry University, Nanjing 210037, China.
This study reports the development of an innovative electrochemical sensor based on organometallic framework nanostructures for detecting valganciclovir (VLCV). VLCV is employed in the treatment of cytomegalovirus retinitis in AIDS patients. Rational design of nanoarchitectures for electroactive materials is a crucial approach for boosting their electrocatalytic performance.
View Article and Find Full Text PDFChemSusChem
December 2024
Sungkyunkwan University, Department of Physics, 2066, Seobu-ro,, Jangan-gu,, 16419, Suwon, KOREA, REPUBLIC OF.
The oxygen evolution reaction (OER) is a critical challenge in electrocatalytic water splitting, hindered by high energy demands and slow kinetics. Polyoxometalates (POMs), recognized for their unique redox capabilities, structural archetypes, and molecular precision, are promising candidates for the oxygen evolution reaction (OER). Yet, their application is hindered by high water solubility, causing rapid degradation and efficiency loss under harsh OER conditions.
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