Electrochemical synthesis of trimetallic nickel-iron-copper nanoparticles via potential-cycling for high current density anion exchange membrane water-splitting applications
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引用次数: 0
Abstract
Hydrogen is known for its elevated energy density and environmental compatibility and is a promising alternative to fossil fuels. Alkaline water electrolysis utilizing renewable energy sources has emerged as a means to obtain high-purity hydrogen. Nevertheless, electrocatalysts used in the process are fabricated using conventional wet chemical synthesis methods, such as sol–gel, hydrothermal, or surfactant-assisted approaches, which often necessitate intricate pretreatment procedures and are vulnerable to post-treatment contamination. Therefore, this study introduces a streamlined and environmentally conscious one-step potential-cycling approach to generate a highly efficient trimetallic nickel-iron-copper electrocatalyst in situ on nickel foam. The synthesized material exhibited remarkable performance, requiring a mere 476 mV to drive electrochemical water splitting at 100 mA cm−2 current density in alkaline solution. Furthermore, this material was integrated into an anion exchange membrane water-splitting device and achieved an exceptionally high current density of 1 A cm−2 at a low cell voltage of 2.13 V, outperforming the noble-metal benchmark (2.51 V). Additionally, ex situ characterizations were employed to detect transformations in the active sites during the catalytic process, revealing the structural transformations and providing inspiration for further design of electrocatalysts.
氢以其高能量密度和环境兼容性而闻名,是一种有前途的化石燃料替代品。利用可再生能源的碱水电解已成为获得高纯度氢的一种手段。然而,该工艺中使用的电催化剂是使用传统的湿化学合成方法制造的,例如溶胶-凝胶,水热或表面活性剂辅助方法,这些方法通常需要复杂的预处理程序,并且容易受到后处理污染。因此,本研究引入了一种流线型的、环保的一步电位循环方法,在泡沫镍上原位生成高效的三金属镍-铁-铜电催化剂。在碱性溶液中,在100 mA cm−2电流密度下,仅需要476 mV就能驱动电化学水分解。此外,将该材料集成到阴离子交换膜水分解装置中,在2.13 V的低电池电压下获得了1 A cm−2的超高电流密度,优于贵金属基准(2.51 V)。此外,采用非原位表征来检测催化过程中活性位点的转变,揭示了结构转变,为进一步设计电催化剂提供了灵感。