Mengling Liu , Qiuping Zhao , Lei Wang , Luyun Chen , Na Shang , Xueliang Wang , Haibin Wang , Chunlei Li , Junying Tian
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引用次数: 0
Abstract
Strong binding affinity for H, CO, and oxygen-containing species of Ru often hinder its electrocatalytic efficiency in hydrogen oxidation reaction (HOR) within alkaline exchange membrane fuel cells (AEMFCs). To address this, a RuNi alloy encased within a carbon shell (Ru0.55Ni0.45@C) is prepared through interchain cross-linking, freeze-drying and carbonization processes. The Ru0.55Ni0.45@C electrcatalyst demonstrates remarkable HOR activity of 526 A gRu−1, surpassing the Pt/C by 2.0 times. Most notably, the electrocatalyst exhibits high tolerance CO. Experimental data indicate that electron transfer from Ni and carbon layer to Ru leads to a decrease in the d-band center of Ru, which in turn reduces both the H and CO binding energy. Additionally, the Ru0.55Ni0.45@C electrocatalyst shows an unusual surge in activity at potentials exceeding 0.375 V vs. RHE. Quasi in situ X-ray photoelectron spectroscopy (XPS) analysis reveals this surge in activity is due to electron enrichment of the Ru component.
在碱性交换膜燃料电池(aemfc)中,钌对H、CO和含氧物质的强结合亲和性往往会阻碍其在氢氧化反应(HOR)中的电催化效率。为了解决这个问题,通过链间交联、冷冻干燥和碳化工艺制备了一种包裹在碳壳内的RuNi合金(Ru0.55Ni0.45@C)。Ru0.55Ni0.45@C电催化剂的HOR活性为526 A gRu−1,是Pt/C的2.0倍。实验数据表明,电子从Ni和碳层转移到Ru,导致Ru的d带中心减小,从而降低了H和CO的结合能。此外,与RHE相比,Ru0.55Ni0.45@C电催化剂在电位超过0.375 V时表现出异常的活性激增。准原位x射线光电子能谱(XPS)分析表明,这种活性的激增是由于Ru成分的电子富集。
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
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