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Extraordinary Performance of Carbon‐Coated Anatase TiO(2) as Sodium‐Ion Anode

The synthesis of in situ polymer‐functionalized anatase TiO(2) particles using an anchoring block copolymer with hydroxamate as coordinating species is reported, which yields nanoparticles (≈11 nm) in multigram scale. Thermal annealing converts the polymer brushes into a uniform and homogeneous carb...

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Detalles Bibliográficos
Autores principales: Tahir, Muhammad Nawaz, Oschmann, Bernd, Buchholz, Daniel, Dou, Xinwei, Lieberwirth, Ingo, Panthöfer, Martin, Tremel, Wolfgang, Zentel, Rudolf, Passerini, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845639/
https://www.ncbi.nlm.nih.gov/pubmed/27134618
http://dx.doi.org/10.1002/aenm.201501489
Descripción
Sumario:The synthesis of in situ polymer‐functionalized anatase TiO(2) particles using an anchoring block copolymer with hydroxamate as coordinating species is reported, which yields nanoparticles (≈11 nm) in multigram scale. Thermal annealing converts the polymer brushes into a uniform and homogeneous carbon coating as proven by high resolution transmission electron microscopy and Raman spectroscopy. The strong impact of particle size as well as carbon coating on the electrochemical performance of anatase TiO(2) is demonstrated. Downsizing the particles leads to higher reversible uptake/release of sodium cations per formula unit TiO(2) (e.g., 0.72 eq. Na(+) (11 nm) vs only 0.56 eq. Na(+) (40 nm)) while the carbon coating improves rate performance. The combination of small particle size and homogeneous carbon coating allows for the excellent electrochemical performance of anatase TiO(2) at high (134 mAh g(−1) at 10 C (3.35 A g(−1))) and low (≈227 mAh g(−1) at 0.1 C) current rates, high cycling stability (full capacity retention between 2nd and 300th cycle at 1 C) and improved coulombic efficiency (≈99.8%).