Poly(vinylferrocene)-Reduced Graphene Oxide as a High Power/High Capacity Cathodic Battery Material

Autor(en): Beladi-Mousavi, Seyyed Mohsen
Sadaf, Shamaila
Walder, Lorenz 
Gallei, Markus
Ruettiger, Christian
Eigler, Siegfried
Halbig, Christian E.
Stichwörter: AQUEOUS DISPERSIONS; CARBON NANOTUBES; Chemistry; Chemistry, Physical; ELECTRICAL-CONDUCTIVITY; ELECTROLYTE-TYPE; Energy & Fuels; FERROCENE; FUNCTIONALIZED GRAPHENE; GRAPHITE OXIDE; Materials Science; Materials Science, Multidisciplinary; ORGANIC-SOLVENTS; Physics; Physics, Applied; Physics, Condensed Matter; RAMAN-SPECTROSCOPY; REDUCTION
Erscheinungsdatum: 2016
Herausgeber: WILEY-V C H VERLAG GMBH
Journal: ADVANCED ENERGY MATERIALS
Volumen: 6
Ausgabe: 12
Zusammenfassung: 
The preparation and performance of a new cathodic battery material consisting of a composite of poly(vinylferrocene) (PVFc) and reduced graphene oxide (rGO) is described. It shows the highest charge/discharge efficiency (at a rate of 100 A g(-1)) ever reported for ferrocene-polymer materials. The composite allows for specific capacities up to 0.21 mAh cm(-2) (770 mC cm(-2), 29 mu m film thickness) at a specific capacity density of 114 mAh g(-1) and less than 5% performance decay over 300 cycles. The composite material is binder free and the charge storing PVFc accounts for 88% of the total weight of the cathodic material. The superb performance is based on (i) perfect self-assembling of oxidized PVFc on graphene oxide (GO) leading to PVFc@GO, (ii) its stepwise (n steps) transfer onto a current collector (CC) (PVFc@GO)(n) @CC (n = drop casting steps), and (iii) the efficient electrochemical transformation of GO into rGO in the composite using viologen as homogeneous electrocatalyst. The self-assembling step is analyzed by zeta potential and atomic force microscopy (AFM) studies, demonstrating heavy ferrocene loading on GO and a mesoporous composite structure, respectively. Complete GO/rGO transition and quantitative ClO4- on breathing of the composite are found by electrochemical quartz crystal microbalance and by electrochemical AFM.
ISSN: 16146832
DOI: 10.1002/aenm.201600108

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