Redox-active Mn is introduced into the B site of redox-stable perovskite niobate-titanate to improve the electrocatalytic activity of composite cathode in an oxide-ion-conducting solid oxide electrolyzer. The XRD and ...Redox-active Mn is introduced into the B site of redox-stable perovskite niobate-titanate to improve the electrocatalytic activity of composite cathode in an oxide-ion-conducting solid oxide electrolyzer. The XRD and XPS results reveal the successful partial replacement of Ti/Nb by Mn in the B site of niobate-titanate. The ionic conductivities of the Mndoped niobate-titanate are significantly improved by approximately 1 order of magnitude in reducing atmosphere and 0.5 order of magnitude in oxidizing atmosphere compared with bare niobate-titanate at 800 ℃. The current efficiency for Mn-doped niobate-titanate cathode is accordingly enhanced by ,-25% and 30% in contrast to the bare cathode with and without reducing gas flowing over the cathode under the applied voltage of 2.0 V at 800 ℃ in an oxide-ion-conducting solid oxide electrolyzer, respectively.展开更多
Ni/YSZ fuel electrodes can only operate under strongly reducing conditions for steam elec- trolysis in an oxide-ion-conducting solid oxide electrolyzer （SOE）. In atmosphere with a low content of H2 or without H2, ca...Ni/YSZ fuel electrodes can only operate under strongly reducing conditions for steam elec- trolysis in an oxide-ion-conducting solid oxide electrolyzer （SOE）. In atmosphere with a low content of H2 or without H2, cathodes based on redox-reversible Nb2TiO7 provide a promising alternative. The reversible changes between oxidized Nb2TiO7 and reduced Nbl.33Tio.6704 samples are systematically investigated after redox-cycling tests. The conductivities of Nb2TiO7 and reduced Nb1.33Tio.6704 are studied as a function of temperature and oxygen partial pressure and correlated with the electrochemical properties of the composite electrodes in a symmetric cell and SOE at 830 ℃. Steam electrolysis is then performed using an oxide-ion-conducting SOE based on a Nb1.33Ti0.6704 composite fuel electrode at 830 ℃. The current-voltage and impedance spectroscopy tests demonstrate that the reduction and activation of the fuel electrode is the main process at low voltage; however, the steam electrolysis dominates the entire process at high voltages. The Faradic efficiencies of steam electrolysis reach 98.9% when 3%H2O/Ar/4%H2 is introduced to the fuel electrode and 89% for that with introduction of 3%H2O/Ar.展开更多
As one of the promising hydrogen production technologies,the development of water electrolysis systems including recycling of their functional components is actively investigated.However,the focus lies on energy and c...As one of the promising hydrogen production technologies,the development of water electrolysis systems including recycling of their functional components is actively investigated.However,the focus lies on energy and chemical intensive metallurgical operations and less on mechanical separation processes in most studies.Here,an innovative surfactant-based separation process(using CTAB and SDS)is investigated to contribute to developing a selective physical separation process for ultrafine particles used in high temperature water electrolyzers(composed of NiO,LSM,ZrO_(2),and YSZ).Their different surface charge in alkaline solutions influences the adsorption of surfactants on particle surfaces as well as the modification of particulate wettability,which is a key separation feature.Through the observations of changes in surface charge and wetting behavior in the presence of surfactants,a feasibility of liquid-liquid particle separation(LLPS)is evaluated.The performance of LLPS with model particle mixtures shows the potential of selective separation with recovery of NiO in the organic phase,while the rest of the particles remain in the aqueous phase.Perovskite LSM is not considered in this system because it shows a high possibility of being recovered by magnetic separation.The proposed process can be further optimized by increasing the phase separation stages,and further research is needed on the NiO phase,which showed exceptional behavior in the presence of the surfactants.展开更多
基金V. ACKNOWLEDGEMENTS This work was supported by the National Natural Science Foundation of China （No.21303037）, China Postdoctoral Science Foundation （No.2013M53150）, and tile Fundamental Research Funds for the Central Univcrsitics （No.2012HGZY0001）.
文摘Redox-active Mn is introduced into the B site of redox-stable perovskite niobate-titanate to improve the electrocatalytic activity of composite cathode in an oxide-ion-conducting solid oxide electrolyzer. The XRD and XPS results reveal the successful partial replacement of Ti/Nb by Mn in the B site of niobate-titanate. The ionic conductivities of the Mndoped niobate-titanate are significantly improved by approximately 1 order of magnitude in reducing atmosphere and 0.5 order of magnitude in oxidizing atmosphere compared with bare niobate-titanate at 800 ℃. The current efficiency for Mn-doped niobate-titanate cathode is accordingly enhanced by ,-25% and 30% in contrast to the bare cathode with and without reducing gas flowing over the cathode under the applied voltage of 2.0 V at 800 ℃ in an oxide-ion-conducting solid oxide electrolyzer, respectively.
文摘Ni/YSZ fuel electrodes can only operate under strongly reducing conditions for steam elec- trolysis in an oxide-ion-conducting solid oxide electrolyzer （SOE）. In atmosphere with a low content of H2 or without H2, cathodes based on redox-reversible Nb2TiO7 provide a promising alternative. The reversible changes between oxidized Nb2TiO7 and reduced Nbl.33Tio.6704 samples are systematically investigated after redox-cycling tests. The conductivities of Nb2TiO7 and reduced Nb1.33Tio.6704 are studied as a function of temperature and oxygen partial pressure and correlated with the electrochemical properties of the composite electrodes in a symmetric cell and SOE at 830 ℃. Steam electrolysis is then performed using an oxide-ion-conducting SOE based on a Nb1.33Ti0.6704 composite fuel electrode at 830 ℃. The current-voltage and impedance spectroscopy tests demonstrate that the reduction and activation of the fuel electrode is the main process at low voltage; however, the steam electrolysis dominates the entire process at high voltages. The Faradic efficiencies of steam electrolysis reach 98.9% when 3%H2O/Ar/4%H2 is introduced to the fuel electrode and 89% for that with introduction of 3%H2O/Ar.
基金the German Federal Ministry for Education and Research(BMBF)for funding of the project ReNaRe-Recycling-Nachhaltige Ressourcennutzung(Grant No.:03HY111D,FeinElSep)as part of the technology platform H2Giga.
文摘As one of the promising hydrogen production technologies,the development of water electrolysis systems including recycling of their functional components is actively investigated.However,the focus lies on energy and chemical intensive metallurgical operations and less on mechanical separation processes in most studies.Here,an innovative surfactant-based separation process(using CTAB and SDS)is investigated to contribute to developing a selective physical separation process for ultrafine particles used in high temperature water electrolyzers(composed of NiO,LSM,ZrO_(2),and YSZ).Their different surface charge in alkaline solutions influences the adsorption of surfactants on particle surfaces as well as the modification of particulate wettability,which is a key separation feature.Through the observations of changes in surface charge and wetting behavior in the presence of surfactants,a feasibility of liquid-liquid particle separation(LLPS)is evaluated.The performance of LLPS with model particle mixtures shows the potential of selective separation with recovery of NiO in the organic phase,while the rest of the particles remain in the aqueous phase.Perovskite LSM is not considered in this system because it shows a high possibility of being recovered by magnetic separation.The proposed process can be further optimized by increasing the phase separation stages,and further research is needed on the NiO phase,which showed exceptional behavior in the presence of the surfactants.
