Pseudocapacitive Heteroatom-Doped Carbon Cathode for Aluminum-Ion Batteries with Ultrahigh Reversible StabilityShow others and affiliations
2024 (English)In: Energy & Environmental Materials, E-ISSN 2575-0356, Vol. 7, no 5, article id e12733Article in journal (Refereed) Published
Abstract [en]
Aluminum (Al)-ion batteries have emerged as a potential alternative to conventional ion batteries that rely on less abundant and costly materials like lithium. Nonetheless, given the nascent stage of advancement in Al-ion batteries (AIBs), attaining electrode materials that can leverage both intercalation capacity and structural stability remains challenging. Herein, we demonstrate a C3N4-derived layered N,S heteroatom-doped carbon, obtained at different pyrolysis temperatures, as a cathode material for AIBs, encompassing the diffusion-controlled intercalation and surface-induced capacity with ultrahigh reversibility. The developed layered N,S-doped corbon (N,S-C) cathode, synthesized at 900 degrees C, delivers a specific capacity of 330 mAh g(-1) with a relatively high coulombic efficiency of similar to 85% after 500 cycles under a current density of 0.5 A g(-1). Owing to its reinforced adsorption capability and enlarged interlayer spacing by doping N and S heteroatoms, the N,S-C900 cathode demonstrates outstanding energy storage capacity with excellent rate performance (61 mAh g(-1) at 20 A g(-1)) and ultrahigh reversibility (90 mAh g(-1) at 5 A g(-1) after 10 000 cycles).
Place, publisher, year, edition, pages
WILEY , 2024. Vol. 7, no 5, article id e12733
Keywords [en]
2D carbon; adsorption energy; heteroatoms-doping; high capacity; long cycling life
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:liu:diva-203441DOI: 10.1002/eem2.12733ISI: 001207832300001Scopus ID: 2-s2.0-85191261480OAI: oai:DiVA.org:liu-203441DiVA, id: diva2:1857547
Note
Funding Agencies|National Natural Science Foundation of China; SSF Synergy Program [EM16-0004]; Swedish Research Council [2022-06725]; [52203092]
2024-05-142024-05-142025-04-05Bibliographically approved