Iron(Fe)nanoparticles and graphite(Gr)with different masses of bismuth trisulfide(Bi_(2)S_(3))were mixed by high-energy ball milling treatment to fabricate the corresponding composite iron anodes Bi_(2)S_(3)@Fe-Gr.The...Iron(Fe)nanoparticles and graphite(Gr)with different masses of bismuth trisulfide(Bi_(2)S_(3))were mixed by high-energy ball milling treatment to fabricate the corresponding composite iron anodes Bi_(2)S_(3)@Fe-Gr.The hydrogen evolution reaction and iron passivation process on these iron electrodes were investigated in alkaline and neutral solutions.The iron electrode Bi_(2)S_(3)-3@Fe-Gr(The additional amount of Bi_(2)S_(3)was 3 mg)revealed the strongest ability to inhibit hydrogen evolution among the iron electrodes of the present investigation,while the Bi_(2)S_(3)-6@Fe-Gr electrode(The additional amount of Bi_(2)S_(3)was 6 mg)delivered significant performance in inhibiting anodic passivation.This is because the high-energy ball milling process leads to the well-dispersion of Bi_(2)S_(3)and the changes in the surface of Fe nanoparticles,thereby slowing down the passivation of the iron electrode surface.展开更多
To extend a new family of aminophosphine-coordinated[FeFe]-hydrogenase mimics for catalytic hydro-gen(H_(2))evolution,we carried out the ligand substitutions of diiron hexacarbonyl precursors[Fe_(2)(μ-X_(2)pdt)(CO)_(...To extend a new family of aminophosphine-coordinated[FeFe]-hydrogenase mimics for catalytic hydro-gen(H_(2))evolution,we carried out the ligand substitutions of diiron hexacarbonyl precursors[Fe_(2)(μ-X_(2)pdt)(CO)_(6)](X_(2)pdt=(SCH_(2))_(2)CX_(2),X=Me,H)with aminodiphosphines(Ph_(2)PCH_(2))_(2)NY(Y=(CH_(2))_(2)OH,(CH_(2))_(3)OH)to obtain two new diiron aminophosphine complexes[Fe_(2)(L1)(μ-Me_(2)pdt)(CO)_(5)](1)and[Fe_(2)(L2)(μ-H_(2)pdt)(CO)_(5)](2),where L1=3-[(diphe-nylphosphaneyl)methyl]oxazolidine,L2=3-[(diphenylphosphaneyl)methyl]-1,3-oxazinane.Moreover,the structures of 1 and 2 have been fully confirmed by elemental analysis,spectroscopic techniques,and single-crystal X-ray diffraction.Using cyclic voltammetry(CV),we investigated the electrochemical redox performance and proton reduc-tion activities of 1 and 2 in acetic acid(HOAc).The CV study indicates that diiron aminophosphine complexes 1 and 2 can be considered to be hydrogenase-inspired diiron molecular electrocatalysts for the reduction of protons into H 2 generation in the presence of HOAc.CCDC:2443967,1;2443969,2.展开更多
A compound containing[FeFe]‑hydrogenase,[Fe_(2)((SCH_(2))_(2)R)(CO)_(6)](1)(R=4‑{(1H‑benzo[d]imidazol‑1‑yl)methyl}‑anilino),was prepared and thoroughly characterized by infrared spectroscopy,single‑crystal X‑ray diffr...A compound containing[FeFe]‑hydrogenase,[Fe_(2)((SCH_(2))_(2)R)(CO)_(6)](1)(R=4‑{(1H‑benzo[d]imidazol‑1‑yl)methyl}‑anilino),was prepared and thoroughly characterized by infrared spectroscopy,single‑crystal X‑ray diffraction,and density functional theory calculations.Its performance as a photocatalyst for hydrogen production via water splitting was evaluated under simulated sunlight.Within 3 h,the amount of H_(2)produced was 386.5μmol,achieving a catalytic efficiency of 25.26μmol·mg^(-1)·h^(-1)and a turnover number(TON)of 0.45.CCDC:2457448.展开更多
In the water-in-oil mieroemulsion system of Triton X-100, 1-hexanol, cyclohexane and Fe（NO3）3 aqueous solution, α－Fe2O3 ultrafine particles were prepared by the method of precipitation using NH3. From transndssion...In the water-in-oil mieroemulsion system of Triton X-100, 1-hexanol, cyclohexane and Fe（NO3）3 aqueous solution, α－Fe2O3 ultrafine particles were prepared by the method of precipitation using NH3. From transndssion electron ndcrographs the mean dianreter of particles is about 3nm. The trifornlity of particle is good. These result have been confirmed by the method of Mossbauer spectrum measurement. The conditions of preparation of α－Fe2O3 ultrallne particles could be controlled easily and the reaction medium could be used cyclically.展开更多
文摘Iron(Fe)nanoparticles and graphite(Gr)with different masses of bismuth trisulfide(Bi_(2)S_(3))were mixed by high-energy ball milling treatment to fabricate the corresponding composite iron anodes Bi_(2)S_(3)@Fe-Gr.The hydrogen evolution reaction and iron passivation process on these iron electrodes were investigated in alkaline and neutral solutions.The iron electrode Bi_(2)S_(3)-3@Fe-Gr(The additional amount of Bi_(2)S_(3)was 3 mg)revealed the strongest ability to inhibit hydrogen evolution among the iron electrodes of the present investigation,while the Bi_(2)S_(3)-6@Fe-Gr electrode(The additional amount of Bi_(2)S_(3)was 6 mg)delivered significant performance in inhibiting anodic passivation.This is because the high-energy ball milling process leads to the well-dispersion of Bi_(2)S_(3)and the changes in the surface of Fe nanoparticles,thereby slowing down the passivation of the iron electrode surface.
文摘To extend a new family of aminophosphine-coordinated[FeFe]-hydrogenase mimics for catalytic hydro-gen(H_(2))evolution,we carried out the ligand substitutions of diiron hexacarbonyl precursors[Fe_(2)(μ-X_(2)pdt)(CO)_(6)](X_(2)pdt=(SCH_(2))_(2)CX_(2),X=Me,H)with aminodiphosphines(Ph_(2)PCH_(2))_(2)NY(Y=(CH_(2))_(2)OH,(CH_(2))_(3)OH)to obtain two new diiron aminophosphine complexes[Fe_(2)(L1)(μ-Me_(2)pdt)(CO)_(5)](1)and[Fe_(2)(L2)(μ-H_(2)pdt)(CO)_(5)](2),where L1=3-[(diphe-nylphosphaneyl)methyl]oxazolidine,L2=3-[(diphenylphosphaneyl)methyl]-1,3-oxazinane.Moreover,the structures of 1 and 2 have been fully confirmed by elemental analysis,spectroscopic techniques,and single-crystal X-ray diffraction.Using cyclic voltammetry(CV),we investigated the electrochemical redox performance and proton reduc-tion activities of 1 and 2 in acetic acid(HOAc).The CV study indicates that diiron aminophosphine complexes 1 and 2 can be considered to be hydrogenase-inspired diiron molecular electrocatalysts for the reduction of protons into H 2 generation in the presence of HOAc.CCDC:2443967,1;2443969,2.
文摘A compound containing[FeFe]‑hydrogenase,[Fe_(2)((SCH_(2))_(2)R)(CO)_(6)](1)(R=4‑{(1H‑benzo[d]imidazol‑1‑yl)methyl}‑anilino),was prepared and thoroughly characterized by infrared spectroscopy,single‑crystal X‑ray diffraction,and density functional theory calculations.Its performance as a photocatalyst for hydrogen production via water splitting was evaluated under simulated sunlight.Within 3 h,the amount of H_(2)produced was 386.5μmol,achieving a catalytic efficiency of 25.26μmol·mg^(-1)·h^(-1)and a turnover number(TON)of 0.45.CCDC:2457448.
文摘In the water-in-oil mieroemulsion system of Triton X-100, 1-hexanol, cyclohexane and Fe（NO3）3 aqueous solution, α－Fe2O3 ultrafine particles were prepared by the method of precipitation using NH3. From transndssion electron ndcrographs the mean dianreter of particles is about 3nm. The trifornlity of particle is good. These result have been confirmed by the method of Mossbauer spectrum measurement. The conditions of preparation of α－Fe2O3 ultrallne particles could be controlled easily and the reaction medium could be used cyclically.
