A reflux-treatment of soluble polyaniline(SPA)in dimethylformamide(DMF)containing CoCl_2 yields an active catalyst for dioxygen reduction which can be adsorbed on the electrode surface firmly.The catalytic reduction o...A reflux-treatment of soluble polyaniline(SPA)in dimethylformamide(DMF)containing CoCl_2 yields an active catalyst for dioxygen reduction which can be adsorbed on the electrode surface firmly.The catalytic reduction of dioxygen at the glassy carbon(GC)electrode modified by the cata- lyst was studied with cyclic voltammetry(CV),rotating disk electrode(RDE)and rotating ring-disk electrode(RRDE).The kinetic process of dioxygen reduction at the modified electrode was analyzed with a new RRDE theory dealing with a nondiffusion-controlled process on ring electrode.The rate constants for each scheme of dioxygen reduction were calculated,showing that only 2-electron reduction to H_2O_2 was conducted at the modified electrode.The effect of solution acidity on the electrocatalytic behaviour for dioxygen reduction was investigated.A possibility of initiating catalytic activity for dioxygen reduction was explored with ESCA method.展开更多
The synthesis and spectroscopic characterization of cobalt(Ⅱ) 5-(4-pyridyl)-10,15,20-triphe- nylporphyrin,cobalt(Ⅱ) 5-(4-N-hexadecylpyridiniumyl)-10,15,20-triphenylporphyrin bromide and cobalt(Ⅱ) 5-(2-aminophenyl)-...The synthesis and spectroscopic characterization of cobalt(Ⅱ) 5-(4-pyridyl)-10,15,20-triphe- nylporphyrin,cobalt(Ⅱ) 5-(4-N-hexadecylpyridiniumyl)-10,15,20-triphenylporphyrin bromide and cobalt(Ⅱ) 5-(2-aminophenyl)-10,15,20-triphenyl-porphyrin are reported.The corresponding copper and vanadyl derivatives ((TriP)Cu,[(hTriP)Cu]^+Br^- and [(hTriP)VO]^+Br^-) were also studied.Each metalloporphyrin was characterized by UV-visible,ESR and ~1H NMR spectroscopy.These me- talloporphyrins can be firmly adsorbed on the glassy carbon (GC) surface.The catalytic reduction of dioxygen at GC electrodes modified by these catalysts was studied by cyclic voltammetry (CV).The kinetic process of dioxygen reduction at the cobalt porphyrin-modified electrodes was studied with a rotating ring disk electrode.展开更多
Hydrogen peroxide has attracted increasing interest as an environmentally benign and green oxidant that can also be used as a solar fuel in fuel cells.This review focuses on recent progress in production of hydrogen p...Hydrogen peroxide has attracted increasing interest as an environmentally benign and green oxidant that can also be used as a solar fuel in fuel cells.This review focuses on recent progress in production of hydrogen peroxide by solar-light-driven oxidation of water by dioxygen and its usage as a green oxidant and fuel.The photocatalytic production of hydrogen peroxide is made possible by combining the e^(-)and 4e-oxidation of water with the e^(-)reduction of dioxygen using solar energy.The catalytic control of the selectivity of the e^(-)vs.4e-oxidation of water is discussed together with the selectivity of the e^(-)vs.4e-reduction of dioxygen.The combination of the photocatalytic e^(-)oxidation of water and the e^(-)reduction of dioxygen provides the best efficiency because both processes afford hydrogen peroxide.The solar-light-driven hydrogen peroxide production by oxidation of water and by reduction of dioxygen is combined with the catalytic oxidation of substrates with hydrogen peroxides,in which dioxygen is used as the greenest oxidant.展开更多
文摘A reflux-treatment of soluble polyaniline(SPA)in dimethylformamide(DMF)containing CoCl_2 yields an active catalyst for dioxygen reduction which can be adsorbed on the electrode surface firmly.The catalytic reduction of dioxygen at the glassy carbon(GC)electrode modified by the cata- lyst was studied with cyclic voltammetry(CV),rotating disk electrode(RDE)and rotating ring-disk electrode(RRDE).The kinetic process of dioxygen reduction at the modified electrode was analyzed with a new RRDE theory dealing with a nondiffusion-controlled process on ring electrode.The rate constants for each scheme of dioxygen reduction were calculated,showing that only 2-electron reduction to H_2O_2 was conducted at the modified electrode.The effect of solution acidity on the electrocatalytic behaviour for dioxygen reduction was investigated.A possibility of initiating catalytic activity for dioxygen reduction was explored with ESCA method.
基金the National Natural Science Foundation of China
文摘The synthesis and spectroscopic characterization of cobalt(Ⅱ) 5-(4-pyridyl)-10,15,20-triphe- nylporphyrin,cobalt(Ⅱ) 5-(4-N-hexadecylpyridiniumyl)-10,15,20-triphenylporphyrin bromide and cobalt(Ⅱ) 5-(2-aminophenyl)-10,15,20-triphenyl-porphyrin are reported.The corresponding copper and vanadyl derivatives ((TriP)Cu,[(hTriP)Cu]^+Br^- and [(hTriP)VO]^+Br^-) were also studied.Each metalloporphyrin was characterized by UV-visible,ESR and ~1H NMR spectroscopy.These me- talloporphyrins can be firmly adsorbed on the glassy carbon (GC) surface.The catalytic reduction of dioxygen at GC electrodes modified by these catalysts was studied by cyclic voltammetry (CV).The kinetic process of dioxygen reduction at the cobalt porphyrin-modified electrodes was studied with a rotating ring disk electrode.
基金supported by the JSPS KAKENHI(16H02268)from MEXTJapan and by the CRI(2012R1A3A2048842)Basic Science Research Program(NRF-2020R1I1A1A01074630)through NRF of Korea.
文摘Hydrogen peroxide has attracted increasing interest as an environmentally benign and green oxidant that can also be used as a solar fuel in fuel cells.This review focuses on recent progress in production of hydrogen peroxide by solar-light-driven oxidation of water by dioxygen and its usage as a green oxidant and fuel.The photocatalytic production of hydrogen peroxide is made possible by combining the e^(-)and 4e-oxidation of water with the e^(-)reduction of dioxygen using solar energy.The catalytic control of the selectivity of the e^(-)vs.4e-oxidation of water is discussed together with the selectivity of the e^(-)vs.4e-reduction of dioxygen.The combination of the photocatalytic e^(-)oxidation of water and the e^(-)reduction of dioxygen provides the best efficiency because both processes afford hydrogen peroxide.The solar-light-driven hydrogen peroxide production by oxidation of water and by reduction of dioxygen is combined with the catalytic oxidation of substrates with hydrogen peroxides,in which dioxygen is used as the greenest oxidant.
