<p>A Fe(III)-iodoargentate hybrid [Fe(DMSO)<sub>6</sub>]Ag<sub>10</sub>I<sub>13</sub> (<b>1</b>) (DMSO = dimethyl sulfoxide) was prepared using a solvated Fe(III) complex cation [Fe(DMSO)<sub>6</sub>]<sup>3+</sup> formed in-situ as the template under solvothermal conditions. It consists of a [Fe(DMSO)<sub>8</sub>]<sup>3+</sup> complex cation, and a 2-D [Ag<sub>10</sub>I<sub>13</sub>]<sub>n</sub><sup>3n‒</sup> layered anion. The 2-D [Ag<sub>10</sub>I<sub>13</sub>]<sub>n</sub><sup>3n‒</sup> anion is composed of ten crystallographically independent AgI<sub>4</sub> tetrahedral units through corner- and edge-sharing, which contains large circles of Ag<sub>7</sub>I<sub>7</sub> with cross sectional dimensions of 7.285 Å × 8.592 Å. Compound <b>1</b> exhibits rapid photocurrent response with steady current density of 4.83 µA·cm<sup>− 2</sup> under visible light irradiation. It shows high photocatalytic activities in the degradation of MB with degradation ratio of 98.8% after light irradiation of 60&#xa0;min.</p>

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Solvothermal synthesis and efficient visible light-driven photocatalytic property of 2-D iodoargentate hybrid directed by solvated Fe(III) cation

  • Hongjin Zhu,
  • Dingxian Jia

摘要

A Fe(III)-iodoargentate hybrid [Fe(DMSO)6]Ag10I13 (1) (DMSO = dimethyl sulfoxide) was prepared using a solvated Fe(III) complex cation [Fe(DMSO)6]3+ formed in-situ as the template under solvothermal conditions. It consists of a [Fe(DMSO)8]3+ complex cation, and a 2-D [Ag10I13]n3n‒ layered anion. The 2-D [Ag10I13]n3n‒ anion is composed of ten crystallographically independent AgI4 tetrahedral units through corner- and edge-sharing, which contains large circles of Ag7I7 with cross sectional dimensions of 7.285 Å × 8.592 Å. Compound 1 exhibits rapid photocurrent response with steady current density of 4.83 µA·cm− 2 under visible light irradiation. It shows high photocatalytic activities in the degradation of MB with degradation ratio of 98.8% after light irradiation of 60 min.