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A new strategy for achieving high K+ storage capacity with fast kinetics: realizing covalent sulfur-rich carbon by phosphorous doping

机译:一个新的策略实现高K +存储能力与快速动力学:实现共价高硫磷掺杂的碳

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摘要

Designing carbon anodes with rich heteroatoms and dilated graphitic interlayer spacing via a one-step synthesis process plays a vital role in accelerating the practical application of potassium ion batteries, but it is still a big challenge. Herein, P-doped S-rich mesoporous carbon (PSMC) is prepared by direct phosphate-assisted carbonization of carrageenan, and it exhibits excellent potassium storage capacity (449 mA h g(-1) at 0.1 A g(-1)), superior rate performance (233 mA h g(-1) at 2 A g(-1)) and long-term stability (97.3% capacity retention after 1000 cycles), due to the high sulfur doping (16.48 wt%) and the coexistence of ordered and disordered regions in the structure. Ex situ characterization, GITT and theoretical calculations reveal that the promotion of covalent sulfur can effectively increase the adsorption of K+ and enhance the K+ reaction kinetics. The proposed one-step synthesis strategy demonstrates the precise use of the composition in biomass, enabling large-scale production of high-performance anodes for K+ storage.
机译:设计与丰富的杂原子和碳阳极膨胀石墨层间间距通过一步法合成过程中起着至关重要的作用加速的实际应用钾离子电池,但它仍然是一个大的挑战。碳(PSMC)是由直接phosphate-assisted碳化的卡拉胶,这展览优秀的钾存储容量(449毫安h g (1) 0.1 g (1)),优越的速度性能(233毫安h g(1)在2g(1))和长期稳定(97.3%产能保留1000周期)后,由于高硫掺杂(16.48 wt %)的共存有序和无序区域的结构。非原位表征,GITT和理论计算表明,促进共价硫可以有效地增加K +的吸附,提高K +的反应动力学。战略演示了精确的使用在生物质成分,使大规模的K +高性能阳极的生产存储。

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