Laser-structured open transport pathways for enhanced electrochemical accessibility in aqueous Cu-Se batteries
Year: 2026
Type: article
Abstract: Selenium (Se) is a promising cathode material for copper (Cu)-ion batteries due to its high volumetric capacity and reversible conversion reactions with Cu ions. However, Se electrodes often suffer from limited electrolyte accessibility and sluggish ion transport, particularly under high-rate conditions. In this study, a nanosecond pulsed laser is employed to fabricate open transport pathways within commercial carbon paper (CP). The morphological changes as a function of laser power and scan speed are systematically analyzed. The optimal results for laser-structured carbon paper (LSCP) are achieved at 600 mm/s and 87.5 W. Insignificant physicochemical changes in LSCP are observed through energy-dispersive X-ray spectroscopy, X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy, making it suitable for Se battery applications. Additionally, insignificant change in weight and crystal structure of Se/C composite are confirmed through thermogravimetric analyzer and XRD, respectively. The LSCP features uniform channels integrated with the porous fibrous CP network, forming a hierarchical transport architecture that promotes electrolyte infiltration, activation of inaccessible Se domains, mass transport, and active surface utilization. Consequently, the Se/LSCP composite cathode achieves a reversible capacity of 952 mAh/g after 1000 cycles at 2 A/g with excellent capacity retention, delivering 512 mAh/g after 4000 cycles at 10 A/g. Electrochemical analyses confirm improved diffusion kinetics and enhanced electrochemical accessibility through the open transport architecture. These findings demonstrate that laser structuring is an effective strategy for enhancing mass transport and maximizing the utilization of Se-based electrodes in aqueous Cu-ion batteries.
Institution: Kongju National University
Language: English
Topic: Aqueous and Flow Batteries
Subfield: Electrical and Electronic Engineering
Field: Engineering
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $1,640
Awards: G2294094328, G9000376040
OpenAlex ID: W7214016554
