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混合金属(氧)氟化物作为一类新型析氧电催化剂的研究。

Investigation of mixed-metal (oxy)fluorides as a new class of water oxidation electrocatalysts.

作者信息

Lemoine Kévin, Lhoste Jérôme, Hémon-Ribaud Annie, Heidary Nina, Maisonneuve Vincent, Guiet Amandine, Kornienko Nikolay

机构信息

Institut des Molécules et Matériaux du Mans (IMMM) , UMR 6283 CNRS , Le Mans Université , Avenue Olivier Messiaen , 72085 Le Mans Cedex 9 , France . Email:

Department of Chemistry , Université de Montréal , Roger-Gaudry Building , Montreal , Quebec H3C 3J7 , Canada . Email:

出版信息

Chem Sci. 2019 Sep 10;10(40):9209-9218. doi: 10.1039/c9sc04027g. eCollection 2019 Oct 28.

DOI:10.1039/c9sc04027g
PMID:32055307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6991172/
Abstract

The development of electrocatalysts for the oxygen evolution reaction (OER) is one of the principal challenges in the area of renewable energy research. Within this context, mixed-metal oxides have recently emerged as the highest performing OER catalysts. Their structural and compositional modification to further boost their activity is crucial to the wide-spread use of electrolysis technologies. In this work, we investigated a series of mixed-metal F-containing materials as OER catalysts to probe possible benefits of the high electronegativity of fluoride ions. We found that crystalline hydrated fluorides, CoFeF(HO) and NiFeF(HO), and amorphous oxyfluorides, NiFeFO and CoFeFO, feature excellent activity (overpotential for 10 mA cm as low as 270 mV) and stability (extended performance for >250 hours with ∼40 mV activity loss) for the OER in alkaline electrolyte. Subsequent electroanalytical and spectroscopic characterization hinted that the electronic structure modulation conferred by the fluoride ions aided their reactivity. Finally, the best catalyst of the set, NiFeFO, was applied as anode in an electrolyzer comprised solely of earth-abundant materials, which carried out overall water splitting at 1.65 V at 10 mA cm.

摘要

开发用于析氧反应(OER)的电催化剂是可再生能源研究领域的主要挑战之一。在此背景下,混合金属氧化物最近已成为性能最高的OER催化剂。对其结构和组成进行改性以进一步提高其活性对于电解技术的广泛应用至关重要。在这项工作中,我们研究了一系列含氟混合金属材料作为OER催化剂,以探究氟离子高电负性可能带来的益处。我们发现,结晶水合氟化物CoFeF(HO)和NiFeF(HO)以及非晶态氧氟化物NiFeFO和CoFeFO在碱性电解质中对OER具有出色的活性(10 mA cm时的过电位低至270 mV)和稳定性(在约40 mV的活性损失下性能可延长>250小时)。随后的电分析和光谱表征表明,氟离子赋予的电子结构调制有助于它们的反应性。最后,该系列中最佳的催化剂NiFeFO被用作仅由储量丰富的材料组成的电解槽的阳极,该电解槽在10 mA cm时于1.65 V下实现了全水分解。

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