首页> 美国卫生研究院文献>Scientific Reports >Plasma engraved Bi0.1(Ba0.5Sr0.5)0.9Co0.8Fe0.2O3−δ perovskite for highly active and durable oxygen evolution
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Plasma engraved Bi0.1(Ba0.5Sr0.5)0.9Co0.8Fe0.2O3−δ perovskite for highly active and durable oxygen evolution

机译:等离子刻有Bi0.1(Ba0.5Sr0.5)0.9Co0.8Fe0.2O3-δ钙钛矿可产生高活性和持久性的氧气

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摘要

The development of highly active and cost-effective catalysts based on noble metal free oxygen electro-catalysis is critical to energy storage and conversion devices. Herein, we highlight a plasma-treated Bi0.1(Ba0.5Sr0.5)0.9Co0.8Fe0.2O3−δ perovskite (denoted as P-Bi0.1BSCF) as a promising catalyst for oxygen evolution reaction (OER) in alkaline media. H2/Ar plasma engraving could significantly increase electrochemically active O22−/O concentration and tune the electronic structure of Co ions efficiently, and consequently tailor the intrinsic electrocatalytic ability for OER. Of note, P-Bi0.1BSCF, with unique crystalline core/amorphous shell structure, exhibits an enhanced intrinsic OER activity and higher stability than the noble metal IrO2 catalyst, which outperforms most of the reported perovskite catalysts. The present work provides new insights into exploring efficient catalysts for OER, and it suggests that, in addition to the extensively applied for surface treatment of various catalysts such as carbons and metal oxides, the plasma engraved perovskite materials also exhibits great potential as precious metal-free catalysts.
机译:基于无金属贵金属氧电催化的高活性和高性价比催化剂的开发对于能量存储和转化装置至关重要。在本文中,我们重点介绍了经过等离子体处理的Bi0.1(Ba0.5Sr0.5)0.9Co0.8Fe0.2O3-δ钙钛矿(表示为P-Bi0.1BSCF),是碱性介质中有希望的氧释放反应(OER)的催化剂。 H2 / Ar等离子体刻蚀可以显着提高电化学活性O2 2- / O -的浓度并有效地调节Co离子的电子结构,从而调整OER的固有电催化能力。值得注意的是,具有独特的结晶核/非晶壳结构的P-Bi0.1BSCF与贵金属IrO2催化剂相比,其表现出的固有OER活性增强,稳定性更高,后者优于大多数报道的钙钛矿催化剂。本工作为探索可用于OER的高效催化剂提供了新见识,它表明,除了广泛用于各种催化剂(如碳和金属氧化物)的表面处理之外,等离子雕刻钙钛矿材料还具有作为贵金属的巨大潜力,游离催化剂。

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