The catalytic performance of two oxides coated anodes （OCSs） meshes and one OCA plate was investigated in a zinc electrowinning electrolyte at 38 ℃. Their electrochemical behaviors were compared with that of a conv...The catalytic performance of two oxides coated anodes （OCSs） meshes and one OCA plate was investigated in a zinc electrowinning electrolyte at 38 ℃. Their electrochemical behaviors were compared with that of a conventional Pb-0.7%Ag alloy anode. Electrochemical measurements such as cyclic voltammetric, galvanostatic, potentiodynamic, open-circuit potential （OCP） and in situ electrochemical noise measurements were considered. After 2 h of OCP test, the linear polarization shows that the corrosion current density of the Ti/（IrO2-Ta2O5） mesh electrode is the lowest （3.37μA/cm^2） among the three OCAs and shows excellent performance. Additionally, after 24 h of galvanostatic polarization at 50 mA/cm^2and 38 ℃, the Ti/MnO2mesh anode has the highest potential （1.799 V）, followed by the Ti/（IrO2-Ta2O5） plate （1.775 V） and Ti/（IrO2-Ta2O5） mesh （1.705 V） anodes. After 24 h of galvanostatic polarization followed by 16 h of decay, the linear polarization method confirms the sequence obtained after 2 h of OCP test, and the Ti/（IrO2-Ta2O5） mesh attains the lowest corrosion current density. The Ti/（IrO2-Ta2O5） mesh anode also shows better performance after 24 h of galvanostatic polarization with the overpotential lower than that of the conventional Pb-Ag anode by about 245 mV.展开更多
Developing non‐noble‐metal electrocatalyst with efficient and durable activity is a urgent task for addressing the sluggish reaction kinetics of electrochemical water oxidation.Structural evolution of the electrocat...Developing non‐noble‐metal electrocatalyst with efficient and durable activity is a urgent task for addressing the sluggish reaction kinetics of electrochemical water oxidation.Structural evolution of the electrocatalyst is an important strategy for achieving enhanced performance.Herein,in situ evolution of surface Co_(2)CrO_(4) to CoOOH/CrOOH(CoOOH/CrOOH‐Co_(2)CrO_(4))by an electrochemical method under alkaline conditions was designed for enhancing the electrocatalytic performance of water oxidation.The experiments demonstrated that the synergy between CoOOH/CrOOH and Co_(2)CrO_(4) resulted in a marked increase in the number of active sites and improved the rate of charge transfer,which enhanced the activity for water oxidation.At a geometrical current density of 20 mA cm^(−2),the overpotential of the oxygen evolution reaction was 244 mV and the turnover frequency was 0.536 s^(−1) in 1.0 M NaOH.展开更多
The increasing exploration of renewable and clean power sources have driven the development of highly active materials for photoelectrochemical （PEC） water splitting. However, it is still a great challenge to enhanc...The increasing exploration of renewable and clean power sources have driven the development of highly active materials for photoelectrochemical （PEC） water splitting. However, it is still a great challenge to enhance the charge utilization. Herein, we report a facile method to fabricate composite photoanode with porous BiVO4 film as the photon absorber and layered double hydroxide （LDH） nanosheet arrays as the oxygen-evolution cocatalysts （OECs）. The as-prepared BiVO4/NiFe-LDH photoanode shows an excellent performance for PEC water splitting benefitting from the synergistic effect of the superior charge separation efficiency facilitated by porous BiVO4 film and the excellent water oxidation activity resulting from LDH nanosheet arrays. A photocurrent density is 4.02 mA cm^-2 at 1.23 V vs. the reversible hydrogen electrode （RHE）. Furthermore, the O2 evolution rate at the surface of BiVO4/NiFe-LDH photoanode is as high as 29.6 μmol h^-1 cm^-2 and the high activity for water oxidation is maintained for over 30 h. Impressively, the performance of the as-fabricated composite photoanode for PEC water splitting can be further enhanced through incorporating a certain amount of Co^2＋ cation into NiFe-LDH as OEC. The photocurrent density is achieved up to 4.45 mA cm^-2 at 1.23 V vs. RHE. This value is the highest yet reported for un-doped BiVO4-based photoanodes so far.展开更多
SnO2 nanosheet films about 200 nm in thickness are successfully fabricated on fluorine-doped tin oxide （FTO） glass by a facile solution-grown approach. The prepared SnO2 nanosheet film is appfied as an interfacial l...SnO2 nanosheet films about 200 nm in thickness are successfully fabricated on fluorine-doped tin oxide （FTO） glass by a facile solution-grown approach. The prepared SnO2 nanosheet film is appfied as an interfacial layer between the nanocrystalline TiO2 film and the FTO substrate in dye-sensitized solar cells （DSCs）. Experimental results show that the introduction of a SnO2 nanosheet film not only suppresses the electron back-transport reaction at the electrolyte/FTO interface but also provides an efficient electron transition channel along the SnO2 nanosheets, and as a result, increasing the open circuit voltage and short current density, and finally improving the conversion efficiency for the DSCs from 3.89% to 4.62%.展开更多
基金Project(RDCPJ 428402)supported by the Natural Sciences and Engineering Research Council of Canada
文摘The catalytic performance of two oxides coated anodes （OCSs） meshes and one OCA plate was investigated in a zinc electrowinning electrolyte at 38 ℃. Their electrochemical behaviors were compared with that of a conventional Pb-0.7%Ag alloy anode. Electrochemical measurements such as cyclic voltammetric, galvanostatic, potentiodynamic, open-circuit potential （OCP） and in situ electrochemical noise measurements were considered. After 2 h of OCP test, the linear polarization shows that the corrosion current density of the Ti/（IrO2-Ta2O5） mesh electrode is the lowest （3.37μA/cm^2） among the three OCAs and shows excellent performance. Additionally, after 24 h of galvanostatic polarization at 50 mA/cm^2and 38 ℃, the Ti/MnO2mesh anode has the highest potential （1.799 V）, followed by the Ti/（IrO2-Ta2O5） plate （1.775 V） and Ti/（IrO2-Ta2O5） mesh （1.705 V） anodes. After 24 h of galvanostatic polarization followed by 16 h of decay, the linear polarization method confirms the sequence obtained after 2 h of OCP test, and the Ti/（IrO2-Ta2O5） mesh attains the lowest corrosion current density. The Ti/（IrO2-Ta2O5） mesh anode also shows better performance after 24 h of galvanostatic polarization with the overpotential lower than that of the conventional Pb-Ag anode by about 245 mV.
文摘Developing non‐noble‐metal electrocatalyst with efficient and durable activity is a urgent task for addressing the sluggish reaction kinetics of electrochemical water oxidation.Structural evolution of the electrocatalyst is an important strategy for achieving enhanced performance.Herein,in situ evolution of surface Co_(2)CrO_(4) to CoOOH/CrOOH(CoOOH/CrOOH‐Co_(2)CrO_(4))by an electrochemical method under alkaline conditions was designed for enhancing the electrocatalytic performance of water oxidation.The experiments demonstrated that the synergy between CoOOH/CrOOH and Co_(2)CrO_(4) resulted in a marked increase in the number of active sites and improved the rate of charge transfer,which enhanced the activity for water oxidation.At a geometrical current density of 20 mA cm^(−2),the overpotential of the oxygen evolution reaction was 244 mV and the turnover frequency was 0.536 s^(−1) in 1.0 M NaOH.
基金supported by the National Natural Science Foundation of China(21422104)the Key Project of Natural Science Foundation of Tianjin City(16JCZDJC30600)
文摘The increasing exploration of renewable and clean power sources have driven the development of highly active materials for photoelectrochemical （PEC） water splitting. However, it is still a great challenge to enhance the charge utilization. Herein, we report a facile method to fabricate composite photoanode with porous BiVO4 film as the photon absorber and layered double hydroxide （LDH） nanosheet arrays as the oxygen-evolution cocatalysts （OECs）. The as-prepared BiVO4/NiFe-LDH photoanode shows an excellent performance for PEC water splitting benefitting from the synergistic effect of the superior charge separation efficiency facilitated by porous BiVO4 film and the excellent water oxidation activity resulting from LDH nanosheet arrays. A photocurrent density is 4.02 mA cm^-2 at 1.23 V vs. the reversible hydrogen electrode （RHE）. Furthermore, the O2 evolution rate at the surface of BiVO4/NiFe-LDH photoanode is as high as 29.6 μmol h^-1 cm^-2 and the high activity for water oxidation is maintained for over 30 h. Impressively, the performance of the as-fabricated composite photoanode for PEC water splitting can be further enhanced through incorporating a certain amount of Co^2＋ cation into NiFe-LDH as OEC. The photocurrent density is achieved up to 4.45 mA cm^-2 at 1.23 V vs. RHE. This value is the highest yet reported for un-doped BiVO4-based photoanodes so far.
基金supported by the National Natural Science Foundation of China (Nos.20903073 and 20671070)the Key Project of Education Ministry of China (No.207008)+1 种基金the Natural Science Foundation of Tianjin (No.09JCYBJC07000)the Science and Technology Developing Foundation for Tianjin Universities (No.20080309)
文摘SnO2 nanosheet films about 200 nm in thickness are successfully fabricated on fluorine-doped tin oxide （FTO） glass by a facile solution-grown approach. The prepared SnO2 nanosheet film is appfied as an interfacial layer between the nanocrystalline TiO2 film and the FTO substrate in dye-sensitized solar cells （DSCs）. Experimental results show that the introduction of a SnO2 nanosheet film not only suppresses the electron back-transport reaction at the electrolyte/FTO interface but also provides an efficient electron transition channel along the SnO2 nanosheets, and as a result, increasing the open circuit voltage and short current density, and finally improving the conversion efficiency for the DSCs from 3.89% to 4.62%.
