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Synthesis of Interface-Driven Tunable Bandgap Metal Oxides AITranslate

Iowa State University; Iowa State University; Iowa State University; Tianjin University; Iowa State University; Tianjin University; Iowa State University; Iowa State University
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Publisher: ACS
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Abstract AITranslate

Mixed bandgap and bandgap tunability in semiconductors is critical in expanding their use. Composition alterations through single-crystal epitaxial growth and the formation of multilayer tandem structures are often employed to achieve mixed bandgaps, albeit with limited tunability. Herein, self-assembled one-dimensional coordination polymers provide facile synthons and templates for graphitic C-doped mesoporous oxides, gC-β-Ga2O3 or gC-In2O3 via controlled oxidative ligand ablation. These materials have mixed bandgaps and colors, depending on amount of gC present. The carbon/oxide interface leads to induced gap states, hence, a stoichiometrically tunable band structure. Structurally, a multiscale porous network percolating throughout the material is realized. The nature of the heat treatment and the top-down process allows for facile tunability and the formation of mixed bandgap metal oxides through controlled carbon deposition. As a proof of concept, gC-β-Ga2O3 was utilized as a photocatalyst for CO2 reduction, which demonstrated excellent conversion rates into CH4 and CO.

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DOI:https://doi.org/10.1021/acsmaterialslett.0c00251

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Citation Information:

Mixed bandgap and bandgap tunability in semiconductors is critical in expanding their use. Composition alterations through single-crystal epitaxial growth and the formation of multilayer tandem structures are often employed to achieve mixed bandgaps, albeit with limited tunability. Herein, self-assembled one-dimensional coordination polymers provide facile synthons and templates for graphitic C-doped mesoporous oxides, gC-β-Ga2O3 or gC-In2O3 via controlled oxidative ligand ablation. These materials have mixed bandgaps and colors, depending on amount of gC present. The carbon/oxide interface leads to induced gap states, hence, a stoichiometrically tunable band structure. Structurally, a multiscale porous network percolating throughout the material is realized. The nature of the heat treatment and the top-down process allows for facile tunability and the formation of mixed bandgap metal oxides through controlled carbon deposition. As a proof of concept, gC-β-Ga2O3 was utilized as a photocatalyst for CO2 reduction, which demonstrated excellent conversion rates into CH4 and CO.

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GB/T 7714-2015 [1] Boyce S. Chang, Andrew Martin, Brijith Thomas, et al. ACS Materials Letters, 2020(2). DOI:10.1021/acsmaterialslett.0c00251.
MLA [1] Boyce S. Chang, et al., ACS Materials Letters, no. 2, 2020, https://doi.org/10.1021/acsmaterialslett.0c00251.
APA [1] Boyce S. Chang, Andrew Martin, Brijith Thomas, Ang Li, Rick W. Dorn, Jinlong Gong, Aaron J. Rossini, & Martin M. Thuo. (2020). ACS Materials Letters(2). https://doi.org/10.1021/acsmaterialslett.0c00251
IEEE [1] Boyce S. Chang, Andrew Martin, Brijith Thomas, Ang Li, Rick W. Dorn, Jinlong Gong, Aaron J. Rossini, and Martin M. Thuo, ACS Materials Letters, no. 2, 2020, doi: 10.1021/acsmaterialslett.0c00251.