To modify the thermodynamics and kinetic performance of magnesium hydride(MgH_(2))for solid-state hydrogen storage,Ni_(3)V_(2)O_(8)-rGO(rGO represents reduced graphene oxide)and Ni_(3)V_(2)O_(8)nanocomposites were pre...To modify the thermodynamics and kinetic performance of magnesium hydride(MgH_(2))for solid-state hydrogen storage,Ni_(3)V_(2)O_(8)-rGO(rGO represents reduced graphene oxide)and Ni_(3)V_(2)O_(8)nanocomposites were prepared by hydrothermal and subsequent heat treatment.The beginning hydrogen desorption temperature of 7 wt.%Ni_(3)V_(2)O_(8)-rGO modified MgH_(2)was reduced to 208°C,while the additive-free MgH_(2)and 7 wt.%Ni_(3)V_(2)O_(8)doped MgH_(2)appeared to discharge hydrogen at 340 and 226°C,respectively.A charging capacity of about 4.7 wt.%H_(2)for MgH_(2)+7 wt.%Ni_(3)V_(2)O_(8)-rGO was achieved at 125°C in 10 min,while the dehydrogenated MgH_(2)took 60 min to absorb only 4.6 wt.%H_(2)at 215°C.The microstructure analysis confirmed that the in-situ generated Mg_(2)Ni/Mg_(2)NiH4 and metallic V contributed significantly to the enhanced performance of MgH_(2).In addition,the presence of rGO in the MgH_(2)+7 wt.%Ni_(3)V_(2)O_(8)-rGO composite reduced particle aggregation tendency of Mg/MgH_(2),leading to improving the cyclic stability of MgH_(2)during 20 cycles.展开更多
Magnesium hydride(MgH_(2)),which possesses high hydrogen density of 7.6 wt%,abundant resource and non-toxicity,has captured intense attention as one of the potential hydrogen storage materials.However,the practical ap...Magnesium hydride(MgH_(2)),which possesses high hydrogen density of 7.6 wt%,abundant resource and non-toxicity,has captured intense attention as one of the potential hydrogen storage materials.However,the practical application of Mg/MgH_(2) system is suffering from high thermal stability,sluggish absorption and desorption kinetics.Herein,two-dimensional(2D) vanadium nanosheets(V_(NS)) were successfully prepared via a facile wet chemical ball milling method and proved to be highly effective on improving the hydrogen storage performance of MgH_(2).For instance,the MgH_(2)+7 wt% V_(NS) composite began to release hydrogen at 187.2℃,152 ℃ lower than that of additive-free MgH_(2).At 300℃,6.3 wt% hydrogen was released from the MgH_(2)+7 wt% V_(NS) composite within 10 min.In addition,the fully dehydrogenated sample could absorb hydrogen even at room temperature under hydrogen pressure of 3.2 MPa.X-ray diffractometer(XRD) and transmission electron microscopy(TEM)results confirmed metallic vanadium served as catalytic unit for facilitating the de/rehydrogenation reaction of MgH_(2).This finding presents an example of facile synthesis of two-dimensional(2D) vanadium with excellent catalysis,which may shed light on future design and preparation of highly effective layered catalysts for hydrogen storage and other energy-related areas.展开更多
The exploration of efficient,long-lived and cost-effective transition metal catalysts is highly desirable for the practical hydrogen storage of magnesium hydride(MgH_(2)) in sustainable energy devices.Herein,FeCoNiCrT...The exploration of efficient,long-lived and cost-effective transition metal catalysts is highly desirable for the practical hydrogen storage of magnesium hydride(MgH_(2)) in sustainable energy devices.Herein,FeCoNiCrTi high-entropy alloy(HEA) nanosheets were prepared via a facile wet chemical ball milling strategy and they were introduced into MgH_(2) to boost the hydrogen storage performance.The refined HEA exhibited superior catalytic activity on MgH_(2).In contrast to additive-free MgH_(2),the initial desorption temperature of the constructed MgH_(2)-HEA composite was reduced from 330.0 to 198.5℃ and a remarkable 51% reduction in the dehydrogenation activation energy was achieved.Besides,the MgH_(2)-HEA composite only required one-twentieth time of that consumed by pure MgH_(2) to absorb 5.0 wt% of H_(2) at 225℃.The synergy between the "hydrogen pumping" effect of Mg_2Ni/Mg_2NiH_4 and Mg_2Co/Mg_2CoH_5 couples,as well as the good dispersion of Fe,Cr and Ti on the surface of MgH_(2) contributed to the enhanced de/hydrogenation performance of the MgH_(2)-HEA composites.This study furnishes important steering for the design and fabrication of multiple transition metal catalysts and may push the commercial application of magnesium-based hydrides one step forward.展开更多
基金financial supports from the National Natural Science Foundation of China (No. 51801078)the Natural Science Foundation of Jiangsu Province, China (No. BK20180986)。
基金the financial support from the National Natural Science Foundation of China(No.51801078).
文摘To modify the thermodynamics and kinetic performance of magnesium hydride(MgH_(2))for solid-state hydrogen storage,Ni_(3)V_(2)O_(8)-rGO(rGO represents reduced graphene oxide)and Ni_(3)V_(2)O_(8)nanocomposites were prepared by hydrothermal and subsequent heat treatment.The beginning hydrogen desorption temperature of 7 wt.%Ni_(3)V_(2)O_(8)-rGO modified MgH_(2)was reduced to 208°C,while the additive-free MgH_(2)and 7 wt.%Ni_(3)V_(2)O_(8)doped MgH_(2)appeared to discharge hydrogen at 340 and 226°C,respectively.A charging capacity of about 4.7 wt.%H_(2)for MgH_(2)+7 wt.%Ni_(3)V_(2)O_(8)-rGO was achieved at 125°C in 10 min,while the dehydrogenated MgH_(2)took 60 min to absorb only 4.6 wt.%H_(2)at 215°C.The microstructure analysis confirmed that the in-situ generated Mg_(2)Ni/Mg_(2)NiH4 and metallic V contributed significantly to the enhanced performance of MgH_(2).In addition,the presence of rGO in the MgH_(2)+7 wt.%Ni_(3)V_(2)O_(8)-rGO composite reduced particle aggregation tendency of Mg/MgH_(2),leading to improving the cyclic stability of MgH_(2)during 20 cycles.
基金financially supported by the National Natural Science Foundation of China(No.51801078)the Natural Science Foundation of Jiangsu Province(No.BK20180986)。
文摘Magnesium hydride(MgH_(2)),which possesses high hydrogen density of 7.6 wt%,abundant resource and non-toxicity,has captured intense attention as one of the potential hydrogen storage materials.However,the practical application of Mg/MgH_(2) system is suffering from high thermal stability,sluggish absorption and desorption kinetics.Herein,two-dimensional(2D) vanadium nanosheets(V_(NS)) were successfully prepared via a facile wet chemical ball milling method and proved to be highly effective on improving the hydrogen storage performance of MgH_(2).For instance,the MgH_(2)+7 wt% V_(NS) composite began to release hydrogen at 187.2℃,152 ℃ lower than that of additive-free MgH_(2).At 300℃,6.3 wt% hydrogen was released from the MgH_(2)+7 wt% V_(NS) composite within 10 min.In addition,the fully dehydrogenated sample could absorb hydrogen even at room temperature under hydrogen pressure of 3.2 MPa.X-ray diffractometer(XRD) and transmission electron microscopy(TEM)results confirmed metallic vanadium served as catalytic unit for facilitating the de/rehydrogenation reaction of MgH_(2).This finding presents an example of facile synthesis of two-dimensional(2D) vanadium with excellent catalysis,which may shed light on future design and preparation of highly effective layered catalysts for hydrogen storage and other energy-related areas.
基金the financial support from the National Natural Science Foundation of China (Grant No.51801078)。
文摘The exploration of efficient,long-lived and cost-effective transition metal catalysts is highly desirable for the practical hydrogen storage of magnesium hydride(MgH_(2)) in sustainable energy devices.Herein,FeCoNiCrTi high-entropy alloy(HEA) nanosheets were prepared via a facile wet chemical ball milling strategy and they were introduced into MgH_(2) to boost the hydrogen storage performance.The refined HEA exhibited superior catalytic activity on MgH_(2).In contrast to additive-free MgH_(2),the initial desorption temperature of the constructed MgH_(2)-HEA composite was reduced from 330.0 to 198.5℃ and a remarkable 51% reduction in the dehydrogenation activation energy was achieved.Besides,the MgH_(2)-HEA composite only required one-twentieth time of that consumed by pure MgH_(2) to absorb 5.0 wt% of H_(2) at 225℃.The synergy between the "hydrogen pumping" effect of Mg_2Ni/Mg_2NiH_4 and Mg_2Co/Mg_2CoH_5 couples,as well as the good dispersion of Fe,Cr and Ti on the surface of MgH_(2) contributed to the enhanced de/hydrogenation performance of the MgH_(2)-HEA composites.This study furnishes important steering for the design and fabrication of multiple transition metal catalysts and may push the commercial application of magnesium-based hydrides one step forward.
