4.8 Article

A copolymer-co-morphology conception for shape-controlled synthesis of Prussian blue analogues and as-derived spinel oxides

Journal

NANOSCALE
Volume 8, Issue 4, Pages 2333-2342

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5nr07193c

Keywords

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Funding

  1. National Natural Science Foundation of China [11079036, 21476232]
  2. Chinese Academy of Sciences Visiting Professorships for Senior International Scientists [2011T1G15, 2013T2G0009]
  3. China-Egypt Scientific Exchange Project of National Natural Science Foundation of China
  4. Academy of Scientific Research and Technology of Egypt [21311140474]
  5. European Research Council [ERC-StG-259709]
  6. 'Lendulet' (Momentum) Program of the Hungarian Academy of Sciences

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The morphologically and compositionally controlled synthesis of coordination polymers and spinel oxides is highly desirable for realizing new advanced nanomaterial functionalities. Here we develop a novel and scalable strategy, containing a copolymer-co-morphology conception, to shape-controlled synthesis of various types of Prussian blue analogues (PBAs). Three series of PBAs MyFe1-y[Co(CN)(6)](0.67)center dot nH(2)O (MyFe1-y-Co, M = Co, Mn and Zn) with well-controlled morphology have been successfully prepared through this strategy. Using MnyFe1-y-Co PBAs as the model, by increasing the relative content of Mn, flexible modulation of the morphology could be easily realized. In addition, a series of porous MnxFe1.8-xCo1.2O4 nano-dices with well-inherited morphologies and defined cation distribution could be obtained through a simple thermal treatment of the PBAs. All these results demonstrate the good universality of this novel strategy. When evaluated as an electrocatalyst, the octahedral-site Mn-III/Mn-IV content in MnxFe1.8-xCo1.2O4, mainly determined by sensitive Fe-57 Mossbauer in combination with X-ray photoelectron spectroscopic techniques, was discovered to be directly correlated with the oxygen reduction/evolution reaction (ORR/OER) activity.

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