Nitrogen and Sulfur Co-doped Mesoporous Carbon for Sodium Ion Batteries
Source abstract
Abstract
Enhanced sodium ion storage capacity of carbon anodes can be realized by heteroatom doping. Designing doped carbons with superior rate performance, high initial Coulombic efficiency (ICE), and excellent cyclability is still vital for practical application of sodium ion batteries. Herein, nitrogen and sulfur co-doped mesoporous carbons have been successfully synthesized from rhodanine using SBA-15 as the template, and the doped carbons exhibit ultrahigh ICE of 90.9%, show superior rate performance with a high capacity of 236 mA h g–1 tested at 10 A g–1, and maintain 88% of their initial capacity even after 5000 cycles in ether-based electrolyte. High nitrogen and sulfur co-doping level, interconnected mesoporous structure, and optimized electrolyte ensure rapid electron/ion transfer. The kinetics analysis indicates that ultrahigh capacitive contribution of 84.5% at 0.2 mV s–1 and 93.9% at 1 mV s–1 can be achieved. Ex situ XPS analysis indicates that heteroatom doping can introduce irreversible capacity, and the functional groups should be strictly controlled for boosting the electrochemical performance. These results open a promising avenue to realize advanced carbon anodes for sodium ion storage by doping with ether-based electrolyte.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Supercapacitor Materials and Fabrication
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering, Ocean University of China, Qingdao 266100, P. R. China
College of Marine Science and Biological Engineering, Qingdao University of Science and Technology, Qingdao 266042, P. R. China
Funding
Ministry of Education of the People's Republic of China · Shandong Province · National Natural Science Foundation of China · Sino-German Center for Research Promotion
References (61)
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