Magnesium hydride(MgH_(2))is the most feasible and effective solid-state hydrogen storage material,which has excellent reversibility but initiates decomposing at high temperatures and has slow kinetics performance.Her...Magnesium hydride(MgH_(2))is the most feasible and effective solid-state hydrogen storage material,which has excellent reversibility but initiates decomposing at high temperatures and has slow kinetics performance.Here,zinc titanate(Zn_(2)TiO_(4))synthesised by the solid-state method was used as an additive to lower the initial temperature for dehydrogenation and enhance the re/dehydrogenation behaviour of MgH_(2).With the presence of Zn_(2)TiO_(4),the starting temperature for the dehydrogenation of MgH_(2)was remarkably lowered to around 290℃–305℃.In addition,within 300 s,the MgH_(2)–Zn_(2)TiO_(4)sample absorbed 5.0 wt.%of H_(2)and 2.2–3.6 wt.%H_(2)was liberated from the composite sample in 30 min,which is faster by 22–36 times than as-milled MgH_(2).The activation energy of the MgH_(2)for the dehydrogenation process was also downshifted to 105.5 k J/mol with the addition of Zn_(2)TiO_(4)indicating a decrease of 22%than as-milled MgH_(2).The superior behaviour of MgH_(2)was due to the formation of Mg Zn_(2),MgO and MgTiO_(3),which are responsible for ameliorating the re/dehydrogenation behaviour of MgH_(2).These findings provide a new understanding of the hydrogen storage behaviour of the catalysed-MgH_(2)system.展开更多
Obviously planar anisotropy due to‘TD split’orthotropic texture(TD indicates Transverse direction)always exist in the Rare-earth(RE)or Ca containing Mg alloy sheets,which is likely caused by the lowreduction rolling...Obviously planar anisotropy due to‘TD split’orthotropic texture(TD indicates Transverse direction)always exist in the Rare-earth(RE)or Ca containing Mg alloy sheets,which is likely caused by the lowreduction rolling(and annealing)as revealed in our previous research.In this work,the as-cast billets of a ZWK100 alloy were subjected to final-pass heavy reduction rolling(FHRR)at 500°C with different reductions(30%-70%)after rough rolling,aiming to investigate the reduction effect on the microstructure and texture formation.The results show that FHRR with higher reductions above 50%is in favor of shear banding formation but has little effect on the as-deformed texture components,and the excellent formability with single-pass reduction up to 70%is mainly ascribed to the activation of prismatic slip.FHRR with reduction above 50%and annealing can generate uniform grain structures of~10μm and symmetrical‘oblique-line split’texture in(0001)pole figures,with basal poles tilting by about 50°from ND(Normal direction)towards some oblique-line of TD and RD(Rolling direction)as well as uniform distribution of counter lines as an annular shape,resulting in excellent elongation to failure of~50%and ultra-low planar anisotropyΔr_of~0.1 and high stretch formability(Erichsen value:8.1).The formation‘oblique-line split’texture in(0001)pole figures is mainly correlated with the preferred growth tendency of grains with■//RD,which was suggested to relate to the high mobility of some special boundaries such as 40°-45°■.The influences of starting textures on the mechanical properties,planar anisotropy and related deformation modes,as well as their correlations with the stretch formability were comparatively investigated with the‘TD split’orthotropic texture as a counterpoint.展开更多
A porous ceramic support is designed as a multi-functional independent catalyst layer for solid oxide fuel cells(SOFCs)running on liquid hydrocarbon fuel.The layer consists of a highly porous Ce_(0.9)Ca_(0.1)O_(2−δ)c...A porous ceramic support is designed as a multi-functional independent catalyst layer for solid oxide fuel cells(SOFCs)running on liquid hydrocarbon fuel.The layer consists of a highly porous Ce_(0.9)Ca_(0.1)O_(2−δ)ceramic backbone and active NiMo catalysts,which could be integrated into the conventional Ni metal containing the anode for internal reforming of the hydrocarbon fuel.Compared to conventional catalyst layers sintered on the anodes,this independent catalyst layer could be simply assembled on top of the anode without additional sintering,thereby avoiding the mismatch of the thermal expansion coefficient between the catalyst layer and the anode and improving stability of a single cell.Moreover,a current collector layer could be inserted between the catalyst and the anode to enhance current collection efficiency and electrochemical performance of the single cell.At 750℃,the independent catalyst layer displays high activity towards the catalytic decomposition of methanol,and the single cell could achieve the maximum power density of 400–500 mW·cm^(−2)in dry methanol.Furthermore,by employing the independent catalyst layer,the single cell offers additional in-situ catalyst regeneration capability under the methanol operation mode.Feeding 10 mL·min−1 air into an anode channel for 5 min is found to be effective to burn out carbon species in the catalyst layer,which reduces the degradation rate of the cell voltage by orders of magnitude from 2.6 to 0.024 mV·h−1 during the operation of 360 h in dry methanol.The results demonstrate the significance of the independent catalyst layer design for direct internal reforming methanol fuel cells.展开更多
基金Universiti Malaysia Terengganu(UMT)for the funding provided by Golden Goose Research Grant(GGRG)VOT 55190。
文摘Magnesium hydride(MgH_(2))is the most feasible and effective solid-state hydrogen storage material,which has excellent reversibility but initiates decomposing at high temperatures and has slow kinetics performance.Here,zinc titanate(Zn_(2)TiO_(4))synthesised by the solid-state method was used as an additive to lower the initial temperature for dehydrogenation and enhance the re/dehydrogenation behaviour of MgH_(2).With the presence of Zn_(2)TiO_(4),the starting temperature for the dehydrogenation of MgH_(2)was remarkably lowered to around 290℃–305℃.In addition,within 300 s,the MgH_(2)–Zn_(2)TiO_(4)sample absorbed 5.0 wt.%of H_(2)and 2.2–3.6 wt.%H_(2)was liberated from the composite sample in 30 min,which is faster by 22–36 times than as-milled MgH_(2).The activation energy of the MgH_(2)for the dehydrogenation process was also downshifted to 105.5 k J/mol with the addition of Zn_(2)TiO_(4)indicating a decrease of 22%than as-milled MgH_(2).The superior behaviour of MgH_(2)was due to the formation of Mg Zn_(2),MgO and MgTiO_(3),which are responsible for ameliorating the re/dehydrogenation behaviour of MgH_(2).These findings provide a new understanding of the hydrogen storage behaviour of the catalysed-MgH_(2)system.
基金financially supported by Basic and Applied Basic Research Fund of Guangdong Province of China(No.2019A1515110573)National Natural Science Foundation of China(No.51901047)+2 种基金Special Innovation Projects of Universities in Guangdong Province(2018KTSCX240)Key Project of Department of Education of Guangdong Province(No.2016GCZX008)Project of Engineering Research Center of Foshan(No.20172010018)。
文摘Obviously planar anisotropy due to‘TD split’orthotropic texture(TD indicates Transverse direction)always exist in the Rare-earth(RE)or Ca containing Mg alloy sheets,which is likely caused by the lowreduction rolling(and annealing)as revealed in our previous research.In this work,the as-cast billets of a ZWK100 alloy were subjected to final-pass heavy reduction rolling(FHRR)at 500°C with different reductions(30%-70%)after rough rolling,aiming to investigate the reduction effect on the microstructure and texture formation.The results show that FHRR with higher reductions above 50%is in favor of shear banding formation but has little effect on the as-deformed texture components,and the excellent formability with single-pass reduction up to 70%is mainly ascribed to the activation of prismatic slip.FHRR with reduction above 50%and annealing can generate uniform grain structures of~10μm and symmetrical‘oblique-line split’texture in(0001)pole figures,with basal poles tilting by about 50°from ND(Normal direction)towards some oblique-line of TD and RD(Rolling direction)as well as uniform distribution of counter lines as an annular shape,resulting in excellent elongation to failure of~50%and ultra-low planar anisotropyΔr_of~0.1 and high stretch formability(Erichsen value:8.1).The formation‘oblique-line split’texture in(0001)pole figures is mainly correlated with the preferred growth tendency of grains with■//RD,which was suggested to relate to the high mobility of some special boundaries such as 40°-45°■.The influences of starting textures on the mechanical properties,planar anisotropy and related deformation modes,as well as their correlations with the stretch formability were comparatively investigated with the‘TD split’orthotropic texture as a counterpoint.
基金support from the National Natural Science Foundation of China(No.22005051)Guangdong Basic and Applied Basic Research Foundation(Nos.2019A1515110237 and 2022A1515012001)+3 种基金Young Creative Talents Project of the Guangdong Provincial Department of Education(No.2019KQNCX166)Innovation Research Project of University in Foshan City(No.2020XCC09).Grateful acknowledgements are extended to the National Natural Science Foundation of China(No.51872047)Key Project Plat Form Programs and Technology Innovation Team Project of Guangdong Provincial Department of Education(Nos.2019KZDXM039,2019GCZX002,and 2020KCXTD011)Guangdong Provincial Key Research and Development Plan(No.2020B090920001)。
文摘A porous ceramic support is designed as a multi-functional independent catalyst layer for solid oxide fuel cells(SOFCs)running on liquid hydrocarbon fuel.The layer consists of a highly porous Ce_(0.9)Ca_(0.1)O_(2−δ)ceramic backbone and active NiMo catalysts,which could be integrated into the conventional Ni metal containing the anode for internal reforming of the hydrocarbon fuel.Compared to conventional catalyst layers sintered on the anodes,this independent catalyst layer could be simply assembled on top of the anode without additional sintering,thereby avoiding the mismatch of the thermal expansion coefficient between the catalyst layer and the anode and improving stability of a single cell.Moreover,a current collector layer could be inserted between the catalyst and the anode to enhance current collection efficiency and electrochemical performance of the single cell.At 750℃,the independent catalyst layer displays high activity towards the catalytic decomposition of methanol,and the single cell could achieve the maximum power density of 400–500 mW·cm^(−2)in dry methanol.Furthermore,by employing the independent catalyst layer,the single cell offers additional in-situ catalyst regeneration capability under the methanol operation mode.Feeding 10 mL·min−1 air into an anode channel for 5 min is found to be effective to burn out carbon species in the catalyst layer,which reduces the degradation rate of the cell voltage by orders of magnitude from 2.6 to 0.024 mV·h−1 during the operation of 360 h in dry methanol.The results demonstrate the significance of the independent catalyst layer design for direct internal reforming methanol fuel cells.