The development of an efficient artificial H_(2)O_(2) photosynthesis system is a challenging work using H_(2)O and O_(2) as starting materials.Herein,3D In_(2.77)S_(4) nanoflower precursor was in-situ deposited on K^(...The development of an efficient artificial H_(2)O_(2) photosynthesis system is a challenging work using H_(2)O and O_(2) as starting materials.Herein,3D In_(2.77)S_(4) nanoflower precursor was in-situ deposited on K^(+)-doped g-C_(3)N_(4)(KCN)nanosheets using a solvothermal method,then In_(2.77)S_(4)/KCN(IS/KCN)het-erojunction with an intimate interface was obtained after a calcination process.The investigation shows that the photocatalytic H_(2)O_(2) production rate of 50IS/KCN can reach up to 1.36 mmol g^(-1)h^(-1)without any sacrificial reagents under visible light irradiation,which is 9.2 times and 4.1 times higher than that of KCN and In_(2.77)S_(4)/respectively.The enhanced activity of the above composite can be mainly attributed to the S-scheme charge transfer route between KCN and In_(2.77)S_(4) according to density functional theory calculations,electron paramagnetic resonance and free radical capture tests,leading to an expanded light response range and rapid charge separation at their interface,as well as preserving the active electrons and holes for H_(2)O_(2) production.Besides,the unique 3D nanostructure and surface hydrophobicity of IS/KCN facilitate the diffusion and transportation of O_(2) around the active centers,the energy barriers of O_(2) protonation and H_(2)O_(2) desorption steps are ef-fectively reduced over the composite.In addition,this system also exhibits excellent light harvesting ability and stability.This work provides a potential strategy to explore a sustainable H_(2)O_(2) photo-synthesis pathway through the design of heterojunctions with intimate interfaces and desired reac-tion thermodynamics and kinetics.展开更多
The Ni 2+/poly(o-aminophenol)electropolymerization was carried out by a continuous cyclic voltammetric scanning at a carbon paste electrode in a mixture of 0.02 mol/L o-aminophenol,0.3 mol/L NiSO 4 and 0.6 mol/L HCl...The Ni 2+/poly(o-aminophenol)electropolymerization was carried out by a continuous cyclic voltammetric scanning at a carbon paste electrode in a mixture of 0.02 mol/L o-aminophenol,0.3 mol/L NiSO 4 and 0.6 mol/L HClO 4.dsDNA was linked to the conducting polymer via three-dimensional structure of polymer film and electrostatic attraction between the negatively charged phosphate backbone of DNA and Ni 2+ ion.The results were testified by the electrochemical methods by using Co(phen)2+3 as an electrochemical indicator.The currents of redox peaks of Co(phen)2+3 increased after immobilizing dsDNA.The conditions for the preparation of Ni 2+/P-OAP/CPE and DNA immobilization were optimized.The voltammetric behavior of dopamine was investigated at the modified electrode.It was found that the modified electrode exhibited a highly electrocatalytic activity toward dopamine oxidation.Differential pulse voltammetry was used for determination of dopamine in pH 5.1 phosphate buffer solution.A linear response of the peak current versus the concentration was found in the range from 5.0×10-6 to 2.0×10-4mol/L with 1.0×10-2 mol/L AA(ascorbic acid)coexisting.The presence of a high concentration of AA did not interfere with the determination.The proposed method exhibits a good recovery and reproducibility.展开更多
文摘The development of an efficient artificial H_(2)O_(2) photosynthesis system is a challenging work using H_(2)O and O_(2) as starting materials.Herein,3D In_(2.77)S_(4) nanoflower precursor was in-situ deposited on K^(+)-doped g-C_(3)N_(4)(KCN)nanosheets using a solvothermal method,then In_(2.77)S_(4)/KCN(IS/KCN)het-erojunction with an intimate interface was obtained after a calcination process.The investigation shows that the photocatalytic H_(2)O_(2) production rate of 50IS/KCN can reach up to 1.36 mmol g^(-1)h^(-1)without any sacrificial reagents under visible light irradiation,which is 9.2 times and 4.1 times higher than that of KCN and In_(2.77)S_(4)/respectively.The enhanced activity of the above composite can be mainly attributed to the S-scheme charge transfer route between KCN and In_(2.77)S_(4) according to density functional theory calculations,electron paramagnetic resonance and free radical capture tests,leading to an expanded light response range and rapid charge separation at their interface,as well as preserving the active electrons and holes for H_(2)O_(2) production.Besides,the unique 3D nanostructure and surface hydrophobicity of IS/KCN facilitate the diffusion and transportation of O_(2) around the active centers,the energy barriers of O_(2) protonation and H_(2)O_(2) desorption steps are ef-fectively reduced over the composite.In addition,this system also exhibits excellent light harvesting ability and stability.This work provides a potential strategy to explore a sustainable H_(2)O_(2) photo-synthesis pathway through the design of heterojunctions with intimate interfaces and desired reac-tion thermodynamics and kinetics.
文摘The Ni 2+/poly(o-aminophenol)electropolymerization was carried out by a continuous cyclic voltammetric scanning at a carbon paste electrode in a mixture of 0.02 mol/L o-aminophenol,0.3 mol/L NiSO 4 and 0.6 mol/L HClO 4.dsDNA was linked to the conducting polymer via three-dimensional structure of polymer film and electrostatic attraction between the negatively charged phosphate backbone of DNA and Ni 2+ ion.The results were testified by the electrochemical methods by using Co(phen)2+3 as an electrochemical indicator.The currents of redox peaks of Co(phen)2+3 increased after immobilizing dsDNA.The conditions for the preparation of Ni 2+/P-OAP/CPE and DNA immobilization were optimized.The voltammetric behavior of dopamine was investigated at the modified electrode.It was found that the modified electrode exhibited a highly electrocatalytic activity toward dopamine oxidation.Differential pulse voltammetry was used for determination of dopamine in pH 5.1 phosphate buffer solution.A linear response of the peak current versus the concentration was found in the range from 5.0×10-6 to 2.0×10-4mol/L with 1.0×10-2 mol/L AA(ascorbic acid)coexisting.The presence of a high concentration of AA did not interfere with the determination.The proposed method exhibits a good recovery and reproducibility.