<p>Amorphous metal oxide (AMO) nanomaterials are attractive because of their unique short-range order structure, but controllable synthesis is still challenging. Here we report a Li<sup>+</sup>-assisted liquid-phase reduction method, which converts a series of crystalline metal oxides into amorphous structures (RuO<sub><i>x</i></sub>, PtO<sub><i>x</i></sub>, CuO<sub><i>x</i></sub>, NiO<sub><i>x</i></sub>, PdO<sub><i>x</i></sub>, MnO<sub><i>x</i></sub> and NiCoO<sub><i>x</i></sub>). Taking RuO<sub>2</sub> as an example, in situ Raman and X-ray absorption spectroscopy indicate that the reduction of Ru–O coordination number and distortion of the medium-range structure of Ru–Ru during the amorphization process are caused by naphthalene radical anions and lithium ions. Theoretical calculations indicate that Li⁺ insertion in RuO<sub><i>x</i></sub> strengthens its electrostatic interaction with the naphthalene radical anion, accelerating the stripping of oxygen from Li⁺-inserted RuO<sub><i>x</i></sub>. The introduction of positive charge by Li⁺ insertion can disrupt the internal charge balance of crystal ruthenium oxide, and therefore reduce the formation energy of intermediates for producing amorphous RuO<sub><i>x</i></sub>. This strategy paves a way for achieving the controllable synthesis of AMOs.</p><p></p>

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Synthesis of amorphous metal oxides via a crystalline to amorphous phase transition strategy

  • Bei Wu,
  • Xiaocheng Liu,
  • Peigen Liu,
  • Geng Wu,
  • Lin Tian,
  • Xiao Han,
  • Junmin Li,
  • Xun Hong

摘要

Amorphous metal oxide (AMO) nanomaterials are attractive because of their unique short-range order structure, but controllable synthesis is still challenging. Here we report a Li+-assisted liquid-phase reduction method, which converts a series of crystalline metal oxides into amorphous structures (RuOx, PtOx, CuOx, NiOx, PdOx, MnOx and NiCoOx). Taking RuO2 as an example, in situ Raman and X-ray absorption spectroscopy indicate that the reduction of Ru–O coordination number and distortion of the medium-range structure of Ru–Ru during the amorphization process are caused by naphthalene radical anions and lithium ions. Theoretical calculations indicate that Li⁺ insertion in RuOx strengthens its electrostatic interaction with the naphthalene radical anion, accelerating the stripping of oxygen from Li⁺-inserted RuOx. The introduction of positive charge by Li⁺ insertion can disrupt the internal charge balance of crystal ruthenium oxide, and therefore reduce the formation energy of intermediates for producing amorphous RuOx. This strategy paves a way for achieving the controllable synthesis of AMOs.