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Identification of carbon-encapsulated iron nanoparticles as active species in non-precious metal oxygen reduction catalysts

机译:在非贵金属氧还原催化剂中鉴定碳包裹的铁纳米颗粒作为活性物种

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The widespread use of fuel cells is currently limited by the lack of efficient and cost-effective catalysts for the oxygen reduction reaction. Iron-based non-precious metal catalysts exhibit promising activity and stability, as an alternative to state-of-the-art platinum catalysts. However, the identity of the active species in non-precious metal catalysts remains elusive, impeding the development of new catalysts. Here we demonstrate the reversible deactivation and reactivation of an iron-based non-precious metal oxygen reduction catalyst achieved using high-temperature gas-phase chlorine and hydrogen treatments. In addition, we observe a decrease in catalyst heterogeneity following treatment with chlorine and hydrogen, using M?ssbauer and X-ray absorption spectroscopy. Our study reveals that protected sites adjacent to iron nanoparticles are responsible for the observed activity and stability of the catalyst. These findings may allow for the design and synthesis of enhanced non-precious metal oxygen reduction catalysts with a higher density of active sites.
机译:当前,燃料电池的广泛使用受到氧还原反应缺乏有效和成本有效的催化剂的限制。铁基非贵金属催化剂表现出有希望的活性和稳定性,可以替代最新的铂催化剂。然而,在非贵金属催化剂中活性物种的身份仍然难以捉摸,这阻碍了新催化剂的开发。在这里,我们证明了使用高温气相氯和氢处理可实现的铁基非贵金属氧还原催化剂的可逆失活和再活化。此外,使用Msssbauer和X射线吸收光谱法,观察到用氯和氢处理后催化剂异质性的降低。我们的研究表明,与铁纳米颗粒相邻的保护位点负责观察到的催化剂活性和稳定性。这些发现可以允许设计和合成具有更高活性位点密度的增强的非贵金属氧还原催化剂。

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