The diverse textures and tunable surface properties of abundant bioresources offer great opportunities to utilize biochar materials as sulfur hosts for naturally boosting the electrochemical performances of Li-S batteries. Herein, a N, S-codoped micro-mesoporous carbon was synthesized from boat-fruited sterculia seed, and used as a sulfur host matrix for Li-S batteries. After sulfur infiltration (≈62% sulfur) and cell assembly, the obtained S/NSBC cathode shows outstanding discharge-charge performance, good rate capability, and especially long cycling stability. A high initial discharge capacity of 1478 mA h g was achieved at 0.1C, and the reversible discharge capacity was still retained at 649 mA h g after 500 cycles at 0.5C with ultralow decay rate of 0.08% per cycle, and especially zero-capacity-decay after 300 cycles. Such superior electrochemical performance of S/NSBC cathode is attributed to the synergy of the unique 3D conductive micro-mesoporous frameworks and huge N, S-codoped polar surface within the carbon matrix, which can physically confine the dissolved polysulfides within the pore structures, and chemically anchor the polysulfides through chemical interaction between lithium polysulfides and N and S sites, thus enabling the favorable reaction kinetics, efficient utilization of sulfur, and effective mitigation of polysulfide diffusion and shuttling within the cathode. This work well manifests the great feasibility and superiority of utilizing bioresources for high performance Li-S batteries.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064315 | PMC |
http://dx.doi.org/10.1039/c9ra02037c | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Harbin Institute of Technology, School of Chemistry and Chemical Engineering, No. 92, West Dazhi Street, 150001, Harbin, CHINA.
Commercial hard carbon (HC) anode suffers from unexpected interphase chemistry rooted in the parasitic reactions between surface oxygen-functional groups and ester-based electrolytes. Herein, an innovative strategy is proposed to regulate interphase chemistry by tailoring targeted functional groups on the HC surface, where highly active undesirable oxygen-functional groups are skillfully converted into a Si-O-Si molecular layer favorable for anchoring anions. Then, an inorganic/organic hybrid solid electrolyte interphase with low interfacial charge transfer resistance and enhanced cycling durability is constructed successfully.
View Article and Find Full Text PDFSci Rep
January 2025
Hangzhou Yanqu Information Technology Co., Ltd., Hangzhou, 310003, Zhejiang, China.
Electrocatalytic materials with dual functions of oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) have received increasing attention in the field of zinc-air batteries (ZABs) research. In this study, bifunctional CoNC@NCXS catalysts were prepared by anchoring Co and N co-doped CoNC on N-doped carbon xerogel sphere (NCXS) based on the spatially confined domain effect and in-situ doping technique. CoNC@NCXS exhibited excellent ORR/OER activity in alkaline electrolytes with the ORR onset potential of 0.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
State Key Laboratory of Physical Chemistry of Solid Surface, Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials, College of Materials, Xiamen University, Xiamen 361005, China.
Sluggish redox kinetics and dendrite growth perplex the fulfillment of efficient electrochemistry in lithium-sulfur (Li-S) batteries. The complicated sulfur phase transformation and sulfur/lithium diversity kinetics necessitate an all-inclusive approach in catalyst design. Herein, a compatible mediator with nanoscale-asymmetric-size configuration by integrating Co single atoms and defective CoTe (Co-CoTe@NHCF) is elaborately developed for regulating sulfur/lithium electrochemistry synchronously.
View Article and Find Full Text PDFRSC Adv
January 2025
Department of Nanoscience and Engineering, Center for Nano Manufacturing, Inje University 197 Inje-ro Gimhae Gyeongnam-do 50834 Republic of Korea
Recently, lithium-sulfur batteries have captivated those in the energy storage industry due to the low cost and high theoretical capacity of the sulfur cathode (1675 mA h g). However, to enhance the practical usability of Li-S batteries, it is crucial to address issues such as the insulating nature of sulfur cathodes and the high solubility of lithium polysulfides (LiPS, LiS , 4 ≤ ≤ 8) that cause poor active sulfur utilization. Designing innovative sulfur hosts can effectively overcome sulfur bottlenecks and achieve stable Li-sulfur batteries.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Innovative Centre for Flexible Devices (iFLEX), Max Planck-NTU Joint Laboratory for Artificial Senses, School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Singapore.
Current lithium batteries experience significant performance degradation under extreme temperature conditions, both high and low. Traditional wide-temperature electrolyte designs typically addressed these challenges by manipulating the solvation sheath and selecting solvents with extreme melting/boiling points. However, these solvent-mediated solutions, while effective at one temperature extreme, invariably fail at the opposite end due to the inherent difficulties in maintaining solvent stability across wide temperatures.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!