4.6 Article

Unearth the understanding of interfacial engineering techniques on nano sulfur cathodes for steady Li-S cell systems

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 8, 期 24, 页码 11976-11985

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta04592f

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资金

  1. National Natural Science Foundation of China [51802269, 21773138]
  2. Chongqing Natural Science Foundation [cstc2018jcyjAX0624]
  3. Fundamental Research Funds for the Central Universities [XDJK2019AA002]
  4. Venture & Innovation Support Program for Chongqing overseas returnees [cx2018027]

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Inherent/tough cell issues such as the troublesome shuttling of intermediate Li2Sn(n= 3-8) and the inferior conductivity of S/Li2S are still hardly eliminated in rechargeable Li-S cells. Continually rationalizing the cathodesviainnovative interfacial engineering would, thereby, be an indispensable propellant for expediting cell kinetics for practical utilizations. By the deliberate choice of nano S cathodes as a typical fundamental research paradigm, we herein affirm a special controllable engineering protocolvia(i)in situpyrrole molecules polymerization on S nanoparticles and (ii)osmosis-driven procedures where inner high-density S atoms tend to be evenly etched/lost. Parameters such as the aging time and persulfate salt addition are verified as dominant factors to tune the exterior shell thickness and S content in samples. To further strengthen the cathode structural integrity and conductivity, virus-like hierarchical S@PPy@ZnIn(2)S(4)products are constructed by the intimate growth of conductive/polar ZnIn(2)S(4)nanolayers on all exterior S@PPy surfaces. Given the positive collaborations from electrode functionality integration and architecture setup, such interface-reinforced cathodes showcase prominent Li-storage performances on either long-lasting cyclic stability/endurance or rate capabilities. This work provides insights into delicate engineering techniques on elemental S for superior Li-S cell systems, and may also open up a smart nano-interface-level platform for more artificial/control designs toward other relatively inert molecular nanocrystals.

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