Ji Kai Liu, Ying Ying Sun, Yi Xiao Wu, Peng Fei Liu, Hua Gui Yang
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引用次数: 0
摘要
工业碱性水电解由于涉及高浓度碱性、频繁的气体解吸和高产氢功率,因此需要具有高耐碱性和可扩展性的催化剂电极。然而,大多数高性能氧进化反应(OER)催化剂与泡沫镍或碳纸等导电基底的附着性很差,导致催化剂在恶劣的工业条件下脱落和性能下降。在此,我们报告了一种简单且可扩展的 "浸泡-红外干燥-煅烧 "策略,可在机械坚固的镍网上原位生长出掺铝尖晶石氧化物。通过进一步简单的阳离子置换,我们有效地调节了八面体中心的金属氧键长度和活性位点的价态,显著提高了 OER 活性。电化学测试(1 M KOH,25 °C)表明,NiAl0.5Co1.5O4 表现出优异的性能,在电流密度为 10 mA cm-2 时,过电位为 234 mV。值得注意的是,在工业条件下(6 M KOH,60 °C),当电流密度为 400 mA cm-2 时,过电位仅为 448 mV,优于商用 Raney Ni 催化剂。此外,这种可扩展电极对浓碱性溶液和高电流密度具有出色的耐受性。
Homogeneous Coating of Al-Doped Spinel Oxides on Ni Mesh for Efficient Oxygen Evolution Reaction
Industrial alkaline water electrolysis requires a catalyst electrode with high alkaline resistance and scalability due to the high alkaline concentration, frequent gas desorption, and high hydrogen production power involved. However, most high-performance oxygen evolution reaction (OER) catalysts are poorly adhered to conductive substrates, such as nickel foam or carbon paper, leading to detachment and performance degradation under harsh industrial conditions. Here, we report a simple and scalable strategy of “immersion-infrared drying-calcination” to fabricate Al-doped spinel oxides in situ grown on mechanically robust Ni mesh. By further simple cation substitution, we effectively modulate the metal-oxygen bond length in the octahedral center and the valence state of active sites, significantly enhancing OER activity. Electrochemical tests (1 M KOH, 25°C) show that NiAl0.5Co1.5O4 exhibits excellent performance with an overpotential of 234 mV at a current density of 10 mA cm−2. Remarkably, under industrial conditions (6 M KOH, 60°C), it achieves an overpotential of only 448 mV at a current density of 400 mA cm−2, which is superior to that of commercial Raney Ni catalysts. Moreover, the scalable electrode demonstrates excellent resistance to concentrated alkaline solutions and high current densities.
期刊介绍:
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