Affiliation:
1. Faculty of Material and Chemistry China University of Geosciences Wuhan 430074 P. R. China
2. Guangxi Key Laboratory of Low Carbon Energy Materials School of Chemical and Pharmaceutical Sciences Guangxi Normal University Guilin 541004 P. R. China
3. School of Physical and Mathematical Sciences Nanyang Technological University Singapore 637371 Singapore
Abstract
AbstractHard carbon (HC) has become the most promising anode material for sodium‐ion batteries (SIBs), but its plateau capacity at ≈0.1 V (Na+/Na) is still much lower than that of graphite (372 mAh g−1) in lithium‐ion batteries (LIBs). Herein, a CO2‐etching strategy is applied to generate abundant closed pores in starch‐derived hard carbon that effectively enhances Na+ plateau storage. During CO2 etching, open pores are first formed on the carbon matrix, which are in situ reorganized to closed pores through high‐temperature carbonization. This CO2‐assisted pore‐regulation strategy increases the diameter and the capacity of closed pores in HC, and simultaneously maintains the microsphere morphology (10–30 µm in diameter). The optimal HC anode exhibits a Na‐storage capacity of 487.6 mAh g−1 with a high initial Coulomb efficiency of 90.56%. A record‐high plateau capacity of 351 mAh g−1 is achieved, owing to the abundant closed micropores generated by CO2‐etching. Comprehensive in situ and ex situ tests unravel that the high Na+ storage performance originates from the pore‐filling mechanism in the closed micropores.
Funder
National Natural Science Foundation of China
Shenzhen Science and Technology Innovation Program
Natural Science Foundation of Zhejiang Province
Subject
General Materials Science,Renewable Energy, Sustainability and the Environment
Cited by
58 articles.
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