Evolution of Ultrathin CoFe-Nanomesh for Oxygen Evolution Reaction: From Slit Pores to Ink-Bottle Pores

IF 3.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemistry - An Asian Journal Pub Date : 2024-11-07 DOI:10.1002/asia.202401156
Shashank Sharma, Amit Paul
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Abstract

The time-dependent mechanism underlying the formation of Co0.8Fe0.2(OH)x-t nanomesh (nanomesh having 80 % Co and 20 % Fe, “t” represents materials synthesis time) has been identified towards the development of a highly effective catalyst for the oxygen evolution reaction (OER). Utilizing 2-ethyl imidazole (2-HEIM) as an etching reagent and the Ostwald ripening process enabled the evolution of nanomesh formation with a precise pore size of ink-bottle shape. Characterization techniques, including N2-adsorption/desorption, and transmission electron microscopy (TEM) analyses, confirmed the evolution of pore structure from layered double hydroxide-like structure to hierarchical slit-pores to uniform ink-bottle pores after 24 h of synthesis with limited pore shrinkage attributable to iron redeposition at the pore entrances. Atomic force microscopy (AFM) showed a gradual reduction in nanomesh thickness with an increase in synthesis time up to 24 h, indicative of successful exfoliation. The best catalyst (Co0.8Fe0.2(OH)x-24 h) was developed after 24 h of synthesis, having 3.8 nm ink-bottle-shaped pores on the basal plane of nanosheets with only 3–4 layers. Co0.8Fe0.2(OH)x-24 h nanomesh exhibited the best catalytic performance, characterized by a 330 mV overpotential, a mass activity of 309.1 A/g, and a turnover frequency of 2.28 s−1. Furthermore, electrochemical impedance spectroscopy indicated a low charge transfer resistance (5.9 Ω) and pseudoresistance (35.3 Ω), highlighting efficient electron transfer at the electrode/electrolyte interface and enhanced oxygen evolution reaction kinetics, respectively. An increased electrochemical surface area (70.74 cm2) and a high roughness factor of approximately 1010 underlined the importance of narrow mesopores in facilitating catalyst-electrolyte interactions and improving mass transport. The best material demonstrated remarkable stability during 25 h of electrolysis with a high average current density of 14.5 mA/cm2. Hence, this research underscores the critical role of pore morphology in nanomeshes for optimizing catalytic performance and providing stability under vigorous gas evolution due to catalysis.

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用于氧进化反应的超薄 CoFe-Nanomesh 的演变:从狭缝孔隙到墨水瓶孔隙。
研究发现了 Co0.8Fe0.2(OH)x-t 纳米网(含 80% Co 和 20% Fe 的纳米网,"t "代表材料合成时间)形成的时间依赖性机理,从而开发出一种用于 OER 的高效催化剂。利用 2- 乙基咪唑作为蚀刻试剂和奥斯特瓦尔德熟化过程,形成了具有墨水瓶形状精确孔径的纳米网。材料表征证实,合成 24 小时后,孔隙结构从层状双氢氧化物样结构演变为分层缝隙孔隙,再演变为均匀的墨水瓶状孔隙,孔隙收缩有限,原因是铁在孔隙入口处重新沉积。原子力显微镜(AFM)显示,随着合成时间的延长,纳米网厚度逐渐减少,直至 24 小时,表明剥离成功。最佳催化剂(Co0.8Fe0.2(OH)x-24h)是在合成 24 小时后形成的,其纳米片基底面上有 3.8 nm 的墨水瓶形孔,只有 3-4 层。Co0.8Fe0.2(OH)x-24h 的催化性能最好,过电位为 330 mV,质量活性为 309.1 A/g ,翻转频率为 2.28 s-1。增加的电化学表面积(70.74 平方厘米)和大约 1010 的高粗糙度系数凸显了狭窄介孔在促进催化剂与电解质相互作用和改善质量传输方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemistry - An Asian Journal
Chemistry - An Asian Journal 化学-化学综合
CiteScore
7.00
自引率
2.40%
发文量
535
审稿时长
1.3 months
期刊介绍: Chemistry—An Asian Journal is an international high-impact journal for chemistry in its broadest sense. The journal covers all aspects of chemistry from biochemistry through organic and inorganic chemistry to physical chemistry, including interdisciplinary topics. Chemistry—An Asian Journal publishes Full Papers, Communications, and Focus Reviews. A professional editorial team headed by Dr. Theresa Kueckmann and an Editorial Board (headed by Professor Susumu Kitagawa) ensure the highest quality of the peer-review process, the contents and the production of the journal. Chemistry—An Asian Journal is published on behalf of the Asian Chemical Editorial Society (ACES), an association of numerous Asian chemical societies, and supported by the Gesellschaft Deutscher Chemiker (GDCh, German Chemical Society), ChemPubSoc Europe, and the Federation of Asian Chemical Societies (FACS).
期刊最新文献
Cover Feature: Evolution of Ultrathin CoFe-Nanomesh for Oxygen Evolution Reaction: From Slit Pores to Ink-Bottle Pores (Chem. Asian J. 4/2025) Front Cover: Covalent Organic Framework Controls the Aggregation of Metal Porphyrins for Enhanced Photocatalytic H2 Evolution (Chem. Asian J. 4/2025) Organophotocatalytic Three-Component Assembly of C4-Cyanoalkylated Phthalazin-1(2H)-Ones. Pd/NHCs-Catalyzed Denitrative/Dechlorinated N-Arylation of Nitroarenes/Chloroarenes to Hydrazine Derivatives. UNUSUAL COORDINATION TYPE OF THE HALOGENATED BIAN LIGANDS IN SILVER(I) COMPLEXES.
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