TY - JOUR
T1 - Synthesis of Interface-Driven Tunable Bandgap Metal Oxides
AU - Chang, Boyce S.
AU - Martin, Andrew
AU - Thomas, Brijith
AU - Li, Ang
AU - Dorn, Rick W.
AU - Gong, Jinlong
AU - Rossini, Aaron J.
AU - Thuo, Martin M.
N1 - Funding Information:
This work was supported by Iowa State University through startup funds, a Royalty account, and a Black and Veatch faculty fellowship to M.T. Solid state NMR spectroscopy (B.T., R.D., and A.J.R.) was supported by the U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences, Materials Science and Engineering Division. The Ames Laboratory is operated for the U.S. DOE by Iowa State University, under Contract No. DE-AC02-07CH11358. A.J.R. thanks Iowa State University and the Ames Laboratory (Royalty Account) for additional support.
Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/9/8
Y1 - 2020/9/8
N2 - 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.
AB - 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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U2 - 10.1021/acsmaterialslett.0c00251
DO - 10.1021/acsmaterialslett.0c00251
M3 - Article
AN - SCOPUS:85092161748
SN - 2639-4979
VL - 2
SP - 1211
EP - 1217
JO - ACS Materials Letters
JF - ACS Materials Letters
IS - 9
ER -