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梁凤丽
招生学科专业:
动力工程及工程热物理 -- 【招收硕士研究生】 -- 能源与动力学院
航空宇航科学与技术 -- 【招收硕士研究生】 -- 能源与动力学院
能源动力 -- 【招收硕士研究生】 -- 能源与动力学院
性别:女
联系方式:15195761621 fengli0912@163.com 学位:工学博士学位

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 硕士生导师 学历:华中科技大学 所在单位:能源与动力学院 办公地点:10-439 电子邮箱:

Amorphous Ni0.75Fe0.25(OH)2-Decorated Layered Double Perovskite Pr0.5Ba0.5CoO3-δfor Highly Efficient and Stable Water Oxidation

点击次数: 所属单位:能源与动力学院 发表刊物:ChemElectroChem 摘要:Highly active, durable, and cost-effective electrocatalysts for water oxidation into oxygen gas hold a key role to realise a range of renewable energy solutions which include water-splitting and rechargeable metal-air batteries. Despite its very stable oxygen evolution reaction (OER) performance over large number of cycles, layered double perovskite PrBaCo2O5+δ(PBC) has a rather limited surface area. It is, thus, desirable to have the stability of PBC combined with the higher OER activity obtained by enlarging its surface area. Here, we used micro-sized PBC particles as the substrate for the deposition of nano-sized nickel-iron hydroxide, Ni0.75Fe0.25(OH)2, which led to an order of magnitude improvement in the OER current density at 1.63 V versus the reversible hydrogen electrode for the amorphous Ni0.75Fe0.25(OH)2-decorated PBC catalyst (A-Ni0.75Fe0.25(OH)2+PBC), relative to the PBC catalyst. We showed that the crystal ordering of the decoration affects the OER activity, that is, the amorphous decoration provided a higher OER activity than the crystalline decoration by enabling a larger contact area between the catalyst and the aqueous electrolyte. The results we show here could potentially stimulate more innovative future works utilising simple chemical preparation route to realise high-performance hybrid OER catalysts involving novel constituents. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 是否译文: 发表时间:2017-03-01 合写作者:Sunarso, Jaka,毛军逵,Yang, Ziqiong,Zhou, Wei 通讯作者:梁凤丽,毛军逵,梁凤丽