用于增强安培级可持续制氢的铈优化无铂高熵合金纳米团簇

Yujia Zhang, Kunkun Nie, Binjie Li, Lixin Yi, Chen Hu, Ziyi Wang, Xiaorong Hao, Wenlin Zhang, Zhengqing Liu, Wei Huang
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引用次数: 0

摘要

在高熵合金(HEA)中加入稀土元素作为氢进化反应(HER)的电催化剂,在解决能源危机方面显示出巨大的潜力。在此,我们采用简便的湿化学合成策略,成功合成了具有化学均匀性和稳定性的铈(Ce)定制 PdCeMoCuRu HEA。所获得的 PdCeMoCuRu HEA 具有丰富的活性金属位点,因此与最先进的 Pt/C 相比,其 HER 性能更为优异。它只需要 12.8 mV 就能达到 10 mA cm 的电流密度,几乎是 Pt/C 所需值(24.8 mV)的一半。重要的是,即使在安培级 1.0 A cm 的高电流密度下,它也能表现出 100 小时的出色电催化耐久性。密度泛函理论(DFT)计算证实,引入 Ce 可以改变电子构型,并在钯、铜和钌活性位点周围产生协同效应。这项工作为设计高效的 RE 定制 HEA 电催化剂提供了一种新方法。
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Cerium-optimized platinum-free high-entropy alloy nanoclusters for enhanced ampere-level sustainable hydrogen generation
The incorporation of rare earth (RE) elements into high-entropy alloys (HEAs) as electrocatalysts for hydrogen evolution reaction (HER) shows great potential in addressing the energy crisis. Here, we successfully synthesized cerium (Ce)-tailored PdCeMoCuRu HEA with chemical homogeneity and stability using a facile wet-chemical synthesis strategy. The obtained PdCeMoCuRu HEA provides abundant active metal sites, resulting in superior HER performance compared to state-of-the-art Pt/C. It only requires 12.8 mV to achieve a current density of 10 mA cm, which is nearly half that required for Pt/C (24.8 mV). Importantly, it exhibits excellent electrocatalytic durability for 100 hours even under a high current density of 1.0 A cm at the ampere level. Density functional theory (DFT) calculations confirm that the introduction of Ce can modify the electronic configuration and generate synergistic effects around Pd, Cu, and Ru active sites. This work establishes a novel approach for designing efficient RE-tailored HEA electrocatalysts.
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