Role of Chloride Ions in the Heat Treatment of β-FeOOH(Cl) Catalysts to Enhance the Oxygen Evolution Reaction Activity

IF 7 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
Takeshi Uyama*, Yusuke Noda, Tomiko M. Suzuki, Keita Sekizawa, Naonari Sakamoto, Takamasa Nonaka and Takeshi Morikawa, 
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引用次数: 0

Abstract

Fe-based catalysts are ideal for the oxygen evolution reaction (OER) owing to their earth abundance. However, most of these catalysts are usable only in an alkaline solution because they dissolve at low pH. Therefore, to be sufficiently versatile for large-scale energy conversion and storage devices, they must maintain high activity over a wide pH range. Cl-stabilized Fe oxyhydroxide, i.e., hollandite-type β-FeOOH(Cl), nanorods have been reported to function in a (nearly) neutral solution with a relatively high activity, which was further improved by heat treatment at ∼200 °C; however, the mechanism underlying this enhancement was poorly understood because of the complicated transformation of β-FeOOH(Cl) to α-Fe2O3 during heating. Therefore, we investigated the structural changes in heat-treated β-FeOOH(Cl) using synchrotron-based X-ray diffraction measurements in addition to several spectroscopic methods and compositional analyses. Structural and compositional analyses, including Rietveld methods, revealed that β-FeOOH(Cl) underwent an indirect phase transformation via a Cl-enriched β-FeOOH(Cl) intermediate phase at 200 °C before α-Fe2O3 formed. The Cl/Fe ratio of the intermediate phase (0.19) was almost twice that of the initial phase (0.08); furthermore, operando X-ray absorption spectroscopy clarified that the Cl-enriched β-FeOOH(Cl) phase was stable during the OER even at a high current density of ∼22 mA cm–2. First-principles calculations using β-FeOOH(Cl) supercell models with Cl/Fe = 0.125 and 0.25 revealed that enrichment with Cl ions increased Cl diffusivity along the tunnel direction in hollandite, notably increasing the electrical conductivity and diffusion coefficient. Both of these properties could enhance the OER activity of β-FeOOH(Cl) catalysts, in addition to previously proposed structural strain. This finding suggests a structure–activity relationship that can serve as a guideline for broadening the use of β-FeOOH(Cl) OER catalysts.

Abstract Image

氯离子在热处理β-FeOOH(Cl)催化剂中提高析氧活性的作用
铁基催化剂由于富含稀土元素,是析氧反应(OER)的理想催化剂。然而,这些催化剂中的大多数只能在碱性溶液中使用,因为它们在低pH下溶解。因此,为了足够多地用于大规模的能量转换和存储设备,它们必须在宽pH范围内保持高活性。据报道,氯稳定的氢氧化铁,即荷兰酸型β-FeOOH(Cl)纳米棒在(接近)中性溶液中发挥作用,具有相对较高的活性,通过在~ 200°C下热处理进一步提高了活性;然而,由于在加热过程中β-FeOOH(Cl)向α-Fe2O3的复杂转变,这种增强的机制尚不清楚。因此,我们利用同步加速器x射线衍射测量以及几种光谱方法和成分分析来研究热处理后β-FeOOH(Cl)的结构变化。采用Rietveld方法对β-FeOOH(Cl)进行了结构和成分分析,发现在α-Fe2O3形成前,β-FeOOH(Cl)在200℃时通过富Cl的β-FeOOH(Cl)中间相发生了间接相变。中间相的Cl/Fe比(0.19)几乎是初始相(0.08)的2倍;此外,operando x射线吸收光谱表明,即使在~ 22 mA cm-2的高电流密度下,富集Cl的β-FeOOH(Cl)相在OER期间也是稳定的。利用Cl/Fe = 0.125和0.25的β-FeOOH(Cl)超级单体模型进行第一性原理计算,发现Cl -离子的富集增加了荷兰石中Cl -沿隧道方向的扩散系数,显著提高了电导率和扩散系数。除了先前提出的结构应变外,这两种性质都可以提高β-FeOOH(Cl)催化剂的OER活性。这一发现提示了一种构效关系,可以作为扩大β-FeOOH(Cl) OER催化剂使用的指导方针。
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来源期刊
Chemistry of Materials
Chemistry of Materials 工程技术-材料科学:综合
CiteScore
14.10
自引率
5.80%
发文量
929
审稿时长
1.5 months
期刊介绍: The journal Chemistry of Materials focuses on publishing original research at the intersection of materials science and chemistry. The studies published in the journal involve chemistry as a prominent component and explore topics such as the design, synthesis, characterization, processing, understanding, and application of functional or potentially functional materials. The journal covers various areas of interest, including inorganic and organic solid-state chemistry, nanomaterials, biomaterials, thin films and polymers, and composite/hybrid materials. The journal particularly seeks papers that highlight the creation or development of innovative materials with novel optical, electrical, magnetic, catalytic, or mechanical properties. It is essential that manuscripts on these topics have a primary focus on the chemistry of materials and represent a significant advancement compared to prior research. Before external reviews are sought, submitted manuscripts undergo a review process by a minimum of two editors to ensure their appropriateness for the journal and the presence of sufficient evidence of a significant advance that will be of broad interest to the materials chemistry community.
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