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A kinetics study on promising hydrogen storage properties of Mg-based thin films at room temperature

机译:镁基薄膜室温储氢特性的动力学研究

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摘要

Pd-Mg-Pd thin films with variable thickness of Mg layers were prepared. Their optical and electrical changes in both gasochromic and chemochromic processes were compared to investigate the kinetics of Mg-based thin films at room temperature. Hydrogen absorption and desorption kinetics of Pd-Mg-Pd thin films were strongly dependent on the thickness of the Mg layer. Especially, when the thickness was lowered to 60 nm, a MgH_2 layer formed immediately after exposure to H_2 at room temperature, while a Mg layer was rapidly generated during hydrogen desorption in ambient air. By means of optical and electrical resistance measurements, we found that the diffusion process contributed significantly to hydrogen absorption and desorption. The remarkable absorption and desorption kinetics at room temperature reported here suggested promising applications in Mg-based energy-efficient devices and hydrogen sensors.
机译:制备了Mg层厚度可变的Pd-Mg-Pd薄膜。比较了它们在气致变色和化学致变色过程中的光学和电学变化,以研究室温下基于Mg的薄膜的动力学。 Pd-Mg-Pd薄膜的氢吸收和解吸动力学强烈依赖于Mg层的厚度。特别地,当厚度减小到60nm时,在室温下暴露于H_2之后立即形成MgH_2层,而在环境空气中的氢解吸期间迅速生成Mg层。通过光学和电阻测量,我们发现扩散过程极大地促进了氢的吸收和解吸。此处报道的室温下出色的吸收和解吸动力学表明在基于Mg的节能设备和氢传感器中的应用前景广阔。

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