{"title":"Evolution of Ultrathin CoFe-Nanomesh for Oxygen Evolution Reaction: From Slit Pores to Ink-Bottle Pores","authors":"Shashank Sharma, Amit Paul","doi":"10.1002/asia.202401156","DOIUrl":null,"url":null,"abstract":"<p>The time-dependent mechanism underlying the formation of Co<sub>0.8</sub>Fe<sub>0.2</sub>(OH)<sub>x</sub>-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 N<sub>2</sub>-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 (Co<sub>0.8</sub>Fe<sub>0.2</sub>(OH)<sub>x</sub>-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. Co<sub>0.8</sub>Fe<sub>0.2</sub>(OH)<sub>x</sub>-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<sup>−1</sup>. 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 cm<sup>2</sup>) 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/cm<sup>2</sup>. 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.</p>","PeriodicalId":145,"journal":{"name":"Chemistry - An Asian Journal","volume":"20 4","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - An Asian Journal","FirstCategoryId":"1","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/asia.202401156","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
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.
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).