Quaternary Wurtzitic Nitrides (1 - x )ZnGeN 2 -2 x GaN ( x = 0.02, 0.05): Disorder-Induced Band-Gap Narrowing and Potentiality as a Solar-Active Photocatalyst

We examined the ZnGeN -GaN solid-solution system (Zn Ge Ga N ) in the unexplored compositional region of < 0.10 to reveal the transitional structural and optical properties caused by the introduction of Ga. Fairly stoichiometric fine powder specimens with compositions of = 0.02 and 0.05 were prep...

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Bibliographic Details
Published inInorganic chemistry Vol. 60; no. 3; pp. 1542 - 1549
Main Authors Suehiro, Takayuki, Tansho, Masataka, Ishigaki, Toru, Shimizu, Tadashi
Format Journal Article
LanguageEnglish
Published United States 01.02.2021
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Summary:We examined the ZnGeN -GaN solid-solution system (Zn Ge Ga N ) in the unexplored compositional region of < 0.10 to reveal the transitional structural and optical properties caused by the introduction of Ga. Fairly stoichiometric fine powder specimens with compositions of = 0.02 and 0.05 were prepared by the gas-reduction-nitridation method, and their partially ordered 2 structure was identified by solid-state Ga NMR spectroscopy and time-of-flight neutron powder diffraction. The Rietveld refinement results of the neutron diffraction data showed that the introduction of 2 atom % Ga readily retards the cation ordering in ZnGeN , and this composition-induced transition to the wurtzite disordered phase proceeds mostly in the range of < 0.10. The synthesized samples showed gradual red shifts of the absorbance and photoluminescence excitation spectra with their value, consistent with their degree of disorder, indicating that the narrowing of the band gap achieved in the current system results primarily from the disorder of the cation sublattice accompanied by octet-rule violation, as has been predicted theoretically. The test reactions for photocatalytic water splitting resulted in improved H evolution rates of 6.1-72.6 μmol/h under UV-visible-light irradiation, and stable solar H evolution of up to 5 days was demonstrated.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.0c02894