Yasukazu Kobayashi*, Sumire Miyakoshi, Luke Murakami, Kanako Utada, Suguru Noda and Nobuko Hanada*,
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引用次数: 0
Abstract
Liquid ammonia electrolysis is a promising route to generate hydrogen. It is performed at room temperature to obtain highly purified hydrogen isolated at the cathode. Theoretically, hydrogen can be extracted by electrolyzing liquid ammonia at a voltage of 0.077 V vs H2/NH3 at 25 °C. However, the onset voltage exceeds the theoretical value in practice owing to the high overpotential associated with the anodic reaction in the amide ion oxidation process. In this study, we prepared high entropy alloy IrRhRuCoNi powder to serve as an anodic catalyst. This powder exhibited a high specific surface area (66.2 m2/g) and was synthesized by reducing the oxide precursor in molten LiCl–CaH2 at 600 °C. A comprehensive structural analysis involving X-ray diffraction and scanning/transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy revealed that the synthesized powder consisted primarily of a face-centered cubic structure with a well-dispersed mixture of Ir, Rh, Ru, Co, and Ni at the nanoscale. The IrRhRuCoNi powder was then supported on carbon nanotubes and used as an anodic catalyst in liquid ammonia electrolysis. Chronoamperometry measurements demonstrated that the anodic catalyst exhibited current densities comparable to a commercial ruthenium black catalyst, reaching 0.93/4.20 mA/cm2 at 0.3/0.5 V vs H2/NH3 after 300 s. Furthermore, the catalytic performance remained stable over a 50 h period. Notably, the alloyed catalyst maintained high current densities of 1.03/3.50 mA/cm2 at 0.3/0.5 V vs H2/NH3 even during cyclic voltammetry measurements at an exceptionally slow scan rate of 2 mV/min from 0 to 0.5 V vs H2/NH3. In contrast, the commercial ruthenium black catalyst exhibited substantial decreases in current densities under these conditions. These results demonstrate the superior performance of the synthesized high entropy alloy IrRhRuCoNi catalyst for liquid ammonia electrolysis compared to the single Ru catalyst, which is likely attributed to the synergistic effects arising from the multielemental composition.
液氨电解是一种很有前途的制氢途径。它在室温下进行,以获得在阴极隔离的高度纯化的氢。理论上,在25℃条件下,以0.077 V vs H2/NH3的电压电解液氨可以提取氢气。然而,在实际应用中,由于酰胺离子氧化过程中阳极反应产生的高过电位,导致起始电压超过理论值。在本研究中,我们制备了高熵合金IrRhRuCoNi粉末作为阳极催化剂。该粉末具有较高的比表面积(66.2 m2/g),在熔融LiCl-CaH2中还原氧化物前驱体,在600℃下合成。通过x射线衍射、扫描/透射电子显微镜以及能量色散x射线光谱的综合结构分析表明,合成的粉末主要由面心立方结构组成,在纳米尺度上由分散良好的Ir、Rh、Ru、Co和Ni混合而成。将制备的IrRhRuCoNi粉末负载在碳纳米管上,用作液氨电解的阳极催化剂。计时安培测量表明,阳极催化剂的电流密度与商业钌黑催化剂相当,在0.3/0.5 V vs H2/NH3下,300 s后达到0.93/4.20 mA/cm2。此外,催化性能在50 h内保持稳定。值得注意的是,合金催化剂在0.3/0.5 V vs H2/NH3下保持了1.03/3.50 mA/cm2的高电流密度,即使在循环伏安法测量中,从0到0.5 V vs H2/NH3的扫描速率为2 mV/min。相比之下,在这些条件下,商用钌黑催化剂的电流密度明显降低。这些结果表明,合成的高熵合金IrRhRuCoNi液氨电解催化剂的性能优于单一Ru催化剂,这可能是由于多元素组成产生的协同效应。
期刊介绍:
ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important energy applications.