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@ARTICLE{Liu:840038,
      author       = {Liu, Haidong and Hu, Huating and Wang, Jun and Niehoff,
                      Philip and He, Xin and Paillard, Elie-Elisée and Eder,
                      Dominik and Winter, Martin and Li, Jie},
      title        = {{H}ierarchical {T}ernary
                      {M}o{O}2/{M}o{S}2/{H}eteroatom-{D}oped {C}arbon {H}ybrid
                      {M}aterials for {H}igh-{P}erformance {L}ithium-{I}on
                      {S}torage},
      journal      = {ChemElectroChem},
      volume       = {3},
      number       = {6},
      issn         = {2196-0216},
      address      = {Weinheim},
      publisher    = {Wiley-VCH},
      reportid     = {FZJ-2017-07604},
      pages        = {922 - 932},
      year         = {2016},
      abstract     = {The synthesis and electrochemical lithium-ion storage
                      behavior of hierarchical MoO2/MoS2/heteroatom-doped carbon
                      (MoO2/MoS2/HD-C) ternary hybrid have been studied. This
                      ternary hybrid is composed of ultrafine MoO2 nanowires and
                      single/few-layer MoS2 encapsulated by heteroatom-doped
                      carbon, constituting secondary cauliflower-like
                      microspheres. The synthesis is achieved through the
                      synergistic interplay of a polymer and an ionic liquid as
                      structure-directing agents and carbon sources, using a
                      solvothermal reaction followed by a simple thermal
                      treatment. In this unique architecture, each component
                      synergistically acts with a specific purpose. The HD-C
                      matrix with abundant defects and vacancies provides fast
                      electronic conduction as well as interfacial storage, and
                      buffers the volume changes during charging/discharging
                      processes. The ultrasmall dimensions of both MoO2 nanowires
                      and single/few-layered MoS2 components enable rapid Li+
                      transport in all directions, which is of great benefit to
                      the reversibility of “conversion” reactions. The
                      hierarchical secondary structures assure the robust
                      stability upon long-term cycling. The ternary hybrid
                      material exhibits enhanced Li+-storage performance as well
                      as reversible capacity, rate capability, and cycling
                      stability. A high reversible specific capacity of
                      1147 mA h g−1 is delivered at 50 mA g−1
                      together with excellent cycling stability, and
                      841 mA h g−1 can be retained after 1000 cycles at
                      500 mA g−1.},
      cin          = {IEK-12},
      ddc          = {540},
      cid          = {I:(DE-Juel1)IEK-12-20141217},
      pnm          = {131 - Electrochemical Storage (POF3-131)},
      pid          = {G:(DE-HGF)POF3-131},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000380045400013},
      doi          = {10.1002/celc.201600062},
      url          = {https://juser.fz-juelich.de/record/840038},
}