@article{JiaFriebeSchubertetal.2019,
  author    = {Jia, He and Friebe, Christian and Schubert, Ulrich S. and Zhang, Xiaozhe and Quan, Ting and Lu, Yan and Gohy, Jean-Francois},
  title     = {Core-Shell Nanoparticles with a Redox Polymer Core and a Silica Porous Shell as High-Performance Cathode Material for Lithium-Ion Batteries},
  series = {Energy technology : generation, conversion, storage, distribution},
  volume    = {8},
  journal   = {Energy technology : generation, conversion, storage, distribution},
  number    = {3},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {2194-4288},
  doi       = {10.1002/ente.201901040},
  pages     = {8},
  year      = {2019},
  abstract  = {A facile and novel method for the fabrication of core-shell nanoparticles (PTMA@SiO2) based on a poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) (PTMA) core and a porous SiO2 shell is reported. The core-shell nanoparticles are further self-assembled with negatively charged multi-walled carbon nanotubes (MWCNTs), which results in the formation of a free-standing cathode electrode. The porous SiO2 shell not only effectively improves the stability of the linear PTMA redox polymer with low molar mass in organic electrolytes but also leads to the uniform dispersion of PTMA active units in the MWCNTs conductive network. The PTMA@SiO2@MWCNT composite electrode exhibits a specific capacity as high as 73.8 mAh g at 1 C and only 0.11\% capacity loss per cycle at a rate of 2 C.},
  language  = {en}
}
@article{HerfurthVollBulleretal.2012,
  author    = {Herfurth, Christoph and Voll, Dominik and Buller, Jens and Weiss, Jan and Barner-Kowollik, Christopher and Laschewsky, Andr{\´e}},
  title     = {Radical addition fragmentation chain transfer (RAFT) polymerization of ferrocenyl (meth)acrylates},
  series = {Journal of polymer science : A, Polymer chemistry},
  volume    = {50},
  journal   = {Journal of polymer science : A, Polymer chemistry},
  number    = {1},
  publisher = {Wiley-Blackwell},
  address   = {Malden},
  issn      = {0887-624X},
  doi       = {10.1002/pola.24994},
  pages     = {108 -- 118},
  year      = {2012},
  abstract  = {We report on the controlled free radical homopolymerization of 1-ferrocenylethyl acrylate as well as of three new ferrocene bearing monomers, namely 4-ferrocenylbutyl acrylate, 2-ferrocenylamido-2-methylpropyl acrylate, and 4-ferrocenylbutyl methacrylate, by the RAFT technique. For comparison, the latter monomer was polymerized using ATRP, too. The ferrocene containing monomers were found to be less reactive than their analogues free of ferrocene. The reasons for the low polymerizability are not entirely clear. As the addition of free ferrocene to the reaction mixture did not notably affect the polymerizations, sterical hindrance by the bulky ferrocene moiety fixed on the monomers seems to be the most probable explanation. Molar masses found for 1-ferrocenylethyl acrylate did not exceed 10,000 g mol(-1), while for 4-ferrocenylbutyl (meth) acrylate molar masses of 15,000 g mol(-1) could be obtained. With PDIs as low as 1.3 in RAFT polymerization of the monomers, good control over the polymerization was achieved.},
  language  = {en}
}