4.8 Article

Sulfur-Rich Graphene Nanoboxes with Ultra-High Potassiation Capacity at Fast Charge: Storage Mechanisms and Device Performance

期刊

ACS NANO
卷 15, 期 1, 页码 1652-1665

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c09290

关键词

sulfur-doping; graphene; potassium sulfur battery; potassium metal battery; hybrid ion capacitor

资金

  1. Shandong Provincial Key RD Plan [2019GGX102038]
  2. Public Welfare Special Program, China [2019GGX102038]
  3. Fundamental Research Funds for the Central Universities [201822008, 201941010]
  4. Qingdao City Programs for Science and Technology Plan Projects [19-6-2-77-cg]
  5. National Natural Science Foundation of China [21775142, 21471139]
  6. Sino-German Center for Research Promotion [GZ 1351]
  7. National Science Foundation, Civil, Mechanical and Manufacturing Innovation (CMMI) [1911905]

向作者/读者索取更多资源

The utilization of sulfur-rich graphene nanoboxes in potassium ion battery and potassium ion capacitor anodes demonstrates exceptional rate capability, high reversible capacity, and outstanding cycling stability, along with revealing insights into the reversible energy storage mechanism and kinetic properties.
It is a major challenge to achieve fast charging and high reversible capacity in potassium ion storing carbons. Here, we synthesized sulfur-rich graphene nanoboxes (SGNs) by one-step chemical vapor deposition to deliver exceptional rate and cyclability performance as potassium ion battery and potassium ion capacitor (PIC) anodes. The SGN electrode exhibits a record reversible capacity of 516 mAh g(-1) at 0.05 A g(-1), record fast charge capacity of 223 mA h g(-1) at 1 A g(-1), and exceptional stability with 89% capacity retention after 1000 cycles. Additionally, the SGN-based PIC displays highly favorable Ragone chart characteristics: 112 Wh kg(-1) at 505 W kg(-1) and 28 Wh kg(-1) at 14618 W kg(-1) with 92% capacity retention after 6000 cycles. X-ray photoelectron spectroscopy analysis illustrates a charge storage sequence based primarily on reversible ion binding at the structural-chemical defects in the carbon and the reversible formation of K-S-C and K2S compounds. Transmission electron microscopy analysis demonstrates reversible dilation of graphene due to ion intercalation, which is a secondary source of capacity at low voltage. This intercalation mechanism is shown to be stable even at cycle 1000. Galvanostatic intermittent titration technique analysis yields diffusion coefficients from 10(-10) to 10(-12) cm(2) s(-1), an order of magnitude higher than S-free carbons. The direct electroanalytic/analytic comparison indicates that chemically bound sulfur increases the number of reversible ion bonding sites, promotes reaction-controlled over diffusion-controlled kinetics, and stabilizes the solid electrolyte interphase. It is also demonstrated that the initial Coulombic efficiency can be significantly improved by switching from a standard carbonate-based electrolyte to an ether-based one.

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