低铱负载酸性水氧化中氧化铱表面的约束最小界面

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Fang-Yi Li, Renxing Huang, Jingwen Jiang, Changhao Liu, Jun Gu and Zhen-Tao Yu*, 
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引用次数: 0

摘要

铱基氧化物具有较好的稳定性,是酸性析氧反应(OER)的最佳工业催化剂。然而,它们的高价格和低OER活动极大地阻碍了它们的商业化。过渡金属掺杂IrO2能显著提高其活性;然而,过渡金属在OER动力学过程中的不稳定性会导致大量的金属溶解和离子交换。本文报道了一种亚稳无定形Fe:IrO2 OER催化剂,该催化剂具有优异的结构柔韧性,以最小的Ir负载提高了催化剂在OER中的性能。其受约束的最小界面结构确保了稳定性,正如时间电位测定测试后铁离子的最小溶解所示。原位FTIR和dem分析表明,该催化剂利用*O - *O自由基偶联机制生成O2。这些发现说明了亚稳态非晶IrO2催化剂在建立稳定优异电化学性能的最佳催化途径方面的重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Constrained Minimal Interface on Iridium Oxide Surfaces for Acidic Water Oxidation with Low Iridium Loading

Constrained Minimal Interface on Iridium Oxide Surfaces for Acidic Water Oxidation with Low Iridium Loading

Iridium-based oxides are the best commercial catalysts for the acidic oxygen evolution reaction (OER) because of their relatively excellent stability. However, their high price and low OER activity have greatly impeded their commercialization. Doping IrO2 with transition metals significantly enhances its activity; however, the instability of transition metals in OER kinetic processes can result in substantial metal dissolution and ion exchange. Herein, we report a metastable amorphous Fe:IrO2 OER catalyst, which provided excellent structural flexibility, enhancing the catalyst’s performance in the OER with minimal Ir loading. Their constrained minimal interface structure ensures stability, as shown by the minimal dissolution of Fe ions after chronopotentiometry tests. In situ FTIR and DEMS analyses reveal that the catalyst utilizes an *O–*O radical coupling mechanism to generate O2. These findings illustrate the important role of metastable amorphous IrO2 catalysts in establishing an optimal catalytic pathway for stable and excellent electrochemical properties.

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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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