Multiple active sites in robust covalent organic frameworks for high-performance lithium/sodium/potassium storage

نویسندگانحیدر رئیسی
نشریهJournal of Energy Storage
شماره صفحات116269-116287
شماره سریال۱۱۷
شماره مجلد۱
نوع مقالهFull Paper
تاریخ انتشار۲۰۲۵
نوع نشریهچاپی
کشور محل چاپهلند
نمایه نشریهJCR،Scopus
کلید واژه هاCovalent organic frameworks Rechargeable alkali metal, ions batteries (LIBs/ SIBs/KIBs) Solid supercapacitors Molecular dynamic simulation Metadynamics technique A B S T R A C T With the escalating demand for portable electronic devices and electric vehicles, there is a critical need for advancements in battery performance metrics. In this context, lithium, sodium, and potassium ion batteries (LIBs, SIBs, and KIBs, respectively) with electrodes based on covalent organic frameworks hold great promise for energy storage. Herein, we applied nanostructures (COFs, COFs@CNT, and functionalized CNTs with carboxyl (, COOH), hydroxyl (, OH), and amino (, NH₂) groups (F, CNT@COFs) as superior materials for energy storage applications, specifically for LIB, SIB, and KIB. Next, the effect of functionalizing with, COOH and, NH₂ groups was analyzed and compared. Furthermore, the Li/Na/K, ion storage mechanism and the substrate structure’

چکیده مقاله

With the escalating demand for portable electronic devices and electric vehicles, there is a critical need for advancements in battery performance metrics. In this context, lithium, sodium, and potassium ion batteries (LIBs, SIBs, and KIBs, respectively) with electrodes based on covalent organic frameworks hold great promise for energy storage. Herein, we applied nanostructures (COFs, COFs@CNT, and functionalized CNTs with carboxyl (–COOH), hydroxyl (–OH), and amino (–NH₂) groups (F-CNT@COFs) as superior materials for energy storage applications, specifically for LIB, SIB, and KIB. Next, the effect of functionalizing with -COOH and -NH₂ groups was analyzed and compared. Furthermore, the Li/Na/K-ion storage mechanism and the substrate structure’s stability were studied through molecular dynamics simulation and well-tempered metadynamics. Moreover, interactions involving π-π stacking between layers of COFs have been proven to enhance the conductivity. Most importantly, the main point is realizing rapid Li/Na/K-ion diffusion kinetics toward the active sites of COFs, COFs@CNTs, and F-CNTs@COFs. Our findings suggest that the movement of Li+ toward the positive electrode material is notably more pronounced than other ions’ migration throughout the charging and discharging processes. Moreover, the storage energy is influenced by active sites, which include contributions from C– –N, C– –O, and the interaction cations-π bonds. In addition, the results of the free energy identified that the energy values for the Li+/COFs and Li+/COOH-CNT@COFs systems at their global minima are approximately ~ − 512.127 kJ mol− 1 and ~ − 650.86 kJ mol− 1, respectively. 1. Introduction Energy plays an essential role in developing both social and environmental facets, thereby bolstering the national economy [1–3]. As time advances, the energy demand steadily escalates in concert with the expansion of the economy and the population. The growing demand for higher energy density and advanced functionalities in electric vehicles, smart grids, and aerospace sectors has spurred significant advancements in supercapacitors and batteries. Among these technologies, rechargeable batteries, such as alkali metal-ion batteries (AMIBs) [4–6], have emerged as promising solutions for addressing the challenge of intermittent power generation. Their advancement is closely tied to the development of improved electrode materials. They are considered ideal energy storage and conversion systems [7] due to their unique characteristics and capabilities. However, advanced AMIBs [8,9] have a high energy density that allows for significant energy storage in a compact design. By effectively managing the intermittent nature of renewable energy, these batteries play a crucial role in mainta

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