首页> 外文期刊>Journal of Materials Chemistry: An Interdisciplinary Journal dealing with Synthesis, Structures, Properties and Applications of Materials, Particulary Those Associated with Advanced Technology >Direct and low energy electrolytic co-reduction of mixed oxides to zirconium-based multi-phase hydrogen storage alloys in molten salts
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Direct and low energy electrolytic co-reduction of mixed oxides to zirconium-based multi-phase hydrogen storage alloys in molten salts

机译:将混合氧化物直接和低能电解共还原为熔融盐中的锆基多相储氢合金

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摘要

Direct synthesis of Zr-based AB2-type hydrogen storage alloys (HSAs) from mixed oxide precursors has been achieved by electrolysis in molten CaCl2 at 900 °C and a cell voltage below 3.2 V. The process resembled direct oxide-to-metal conversion in solid state, and the target alloys, namely ZrCr2, ZrCr_(0.7)Ni_(1.3)and Zr_(0.5)Ti_(0.5)V_(0.5)Cr_(0.2)Ni_(1.3), were formed in situ during electrolysis without going through any melting step. Electrolysis energy consumption could be as low as 9.59 kWh (kg-HSA)~(-1) and the metal recovery yield was generally higher than 90%. The electrolytic products were readily obtained as powders with the designated compositions and crystal structures (e.g. the C14 and C15 Laves phases). More importantly, these Zr-based electrolytic HSA powders were composed of nodular micro-particles which are very desirable for fabrication of electrodes with micro-porosity to facilitate electrolyte ex-and ingression. Galvanostatic discharge-charge tests of the as-prepared electrolytic HSA powders resulted in similar or higher hydrogen storage capacities (up to 280 mAh g~(-1)) in comparison with the same HSAs prepared by e.g. arc-melting the individual metals as reported in literature. Particularly, the electrolytic Zr-based HSAs were unique for their high initial capacities without any pre-treatment for activation, and they also exhibited highly satisfactory discharge rate capability with less than 20% capacity loss when the discharge current increased from 50 to 600 mA g~(-1).
机译:通过在900°C且在低于3.2 V的电池电压下在熔融的CaCl2中进行电解,已经可以从混合氧化物前驱体直接合成Zr基AB2型储氢合金(HSA)。该过程类似于直接氧化转化为金属的过程。固态,在电解过程中原位形成ZrCr2,ZrCr_(0.7)Ni_(1.3)和Zr_(0.5)Ti_(0.5)V_(0.5)Cr_(0.2)Ni_(1.3)的目标合金任何熔化步骤。电解能耗可低至9.59 kWh(kg-HSA)〜(-1),金属回收率通常高于90%。容易获得具有指定组成和晶体结构(例如C14和C15 Laves相)的粉末形式的电解产物。更重要的是,这些基于Zr的电解HSA粉末由球状微粒组成,这对于制造具有微孔结构的电极非常有利,以利于电解质的进出。所制备的电解HSA粉末的恒电流充放电试验与通过例如HPLC制备的相同HSA相比,储氢容量相似或更高(高达280 mAh g〜(-1))。如文献报道的,电弧熔化每种金属。尤其是,基于Zr的电解HSA的独特之处在于其高初始容量,无需进行任何活化前处理,并且当放电电流从50 mA增加到600 mA g时,它们还显示出令人满意的放电速率能力,且容量损失小于20% 〜(-1)。

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