TY - JOUR
T1 - Oxidation Anchoring Cross-Linking Strategy Synthesis of Semicoke-Based Hard Carbon for Low-Cost and High-Performance Sodium-Ion Batteries
AU - Wang, Yingying
AU - Zhang, Yue
AU - Ma, Huizhen
AU - Tang, Yakun
AU - Dai, Mengyao
AU - Liu, Lang
AU - Cao, Yuliang
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/7/2
Y1 - 2025/7/2
N2 - Semicoke is extensively utilized in the production of carbon-based materials due to its advantages of high carbon yield and low cost. However, as a thermoplastic precursor, it tends to undergo melting and reorganization during thermal decomposition, resulting in the formation of a well-structured graphite lattice, which limits its application in sodium storage. Herein, we introduce an oxidation anchoring cross-linking strategy to synthesize semicoke-based hard carbon (SBHC). This approach effectively incorporates C-O-C and −C(O)-O- functional groups into the semicoke molecules. The introduced oxygen functional groups (OFGs) will enlarge the interlayer spacing and form a more nanoporous structure in the bulk of hard carbon. The optimized SBHC demonstrates a significantly enhanced reversible capacity of 280.84 mAh g-1, which significantly surpasses the capacity of the raw semicoke-derived hard carbon (134.53 mAh g-1), with the plateau capacity increase of 2.6 times. This study presents a viable strategy for producing cost-effective, high-performance hard carbon materials for sodium-ion batteries.
AB - Semicoke is extensively utilized in the production of carbon-based materials due to its advantages of high carbon yield and low cost. However, as a thermoplastic precursor, it tends to undergo melting and reorganization during thermal decomposition, resulting in the formation of a well-structured graphite lattice, which limits its application in sodium storage. Herein, we introduce an oxidation anchoring cross-linking strategy to synthesize semicoke-based hard carbon (SBHC). This approach effectively incorporates C-O-C and −C(O)-O- functional groups into the semicoke molecules. The introduced oxygen functional groups (OFGs) will enlarge the interlayer spacing and form a more nanoporous structure in the bulk of hard carbon. The optimized SBHC demonstrates a significantly enhanced reversible capacity of 280.84 mAh g-1, which significantly surpasses the capacity of the raw semicoke-derived hard carbon (134.53 mAh g-1), with the plateau capacity increase of 2.6 times. This study presents a viable strategy for producing cost-effective, high-performance hard carbon materials for sodium-ion batteries.
UR - https://www.scopus.com/pages/publications/105009541523
U2 - 10.1021/acs.langmuir.5c01677
DO - 10.1021/acs.langmuir.5c01677
M3 - Article
AN - SCOPUS:105009541523
SN - 0743-7463
JO - Langmuir
JF - Langmuir
ER -