Puchang Hou , Ruizhe Ru , Ziyong Zhang , Jinyan Xie , Lei Zhang , Fei Han , Guowei Li , Jun-Qiang Wang , Juntao Huo
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引用次数: 0
Abstract
The sluggish four-electron oxygen evolution reaction (OER) with a high kinetic barrier remains the major bottleneck for industrial alkaline water electrolysis, motivating the development of efficient and durable non-noble metal catalysts. Multicomponent alloying offers a powerful route to tune OER-active sites through inter-element electronic interactions and synergistic redox chemistry. However, the enormous compositional space makes the rational optimization of elemental ratios labor-intensive and scientifically challenging. Here, we establish a product-bubble-based high-throughput screening strategy that directly correlates oxygen bubble evolution behavior with catalytic activity, enabling rapid identification of promising compositions from a continuously varied Al–Co–Ni–Fe–Mo multicomponent alloy library. Guided by this screening, we synthesize the target composition Al32Co37.5Ni8.5Fe10Mo12 on nickel foam and further activate it via dealloying. Dealloying induces in situ reconstruction into vertically aligned nanosheet arrays, selectively leaches Al, enriches Co at the surface, and promotes the formation of high-valence metal species. As a result, the dealloyed sample delivers low overpotentials of 269 mV and 312 mV at 10 and 100 mA cm−2 in 1.0 M KOH, respectively, and maintains stable operation at both current densities. This work provides a fast and intuitive pathway for screening and designing non-precious multicomponent OER catalysts with promising potential for practical water electrolysis applications.
缓慢的四电子析氧反应(OER)具有较高的动力学势垒,仍然是工业碱水电解的主要瓶颈,推动着高效、耐用的非贵金属催化剂的发展。多组分合金化通过元素间电子相互作用和协同氧化还原化学,为调整oer活性位点提供了强有力的途径。然而,巨大的构成空间使得元素比例的合理优化成为劳动密集型和科学挑战。在这里,我们建立了一种基于产品气泡的高通量筛选策略,将氧气泡演化行为与催化活性直接联系起来,从而能够从连续变化的Al-Co-Ni-Fe-Mo多组分合金库中快速识别有希望的成分。在此筛选的指导下,我们在泡沫镍上合成了目标组合物Al32Co37.5Ni8.5Fe10Mo12,并通过合金化进一步活化。脱合金诱导原位重构成垂直排列的纳米片阵列,选择性地浸出Al,在表面富集Co,促进高价金属物质的形成。结果表明,合金样品在1.0 M KOH条件下,在10和100 mA cm−2条件下的过电位分别为269 mV和312 mV,并在两种电流密度下保持稳定运行。这项工作为筛选和设计非贵重多组分OER催化剂提供了一种快速直观的途径,具有实际水电解应用的潜力。
期刊介绍:
A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
Impact factor: 5.0
Time to first decision (peer reviewed only): 31 days