2017
DOI: 10.1007/s10854-017-6499-0
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Novel microwave-assisted synthesis of leaf-like MnMoO4 nanostructures and investigation of their photocatalytic performance

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Cited by 25 publications
(7 citation statements)
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“…X-ray diffraction (XRD) patterns were then used to present the phase component of the catalysts. As illustrated in Figure a, the diffraction peaks of the neat Mn- or Mo-based oxide were in good accordance with the standard patterns of Mn 2 O 3 (JCPDS-71-0636) at 23.1, 32.9, 38.2, 45.1, 49.3, 55.1, and 65.7° corresponding to the (211), (222), (400), (332), (431), and (440) crystal planes and those of MoO 3 (JCPDS-99-0080) at 12.8, 23.3, 25.9, 27.3, 33.7, 40.0, 49.2, and 58.8° corresponding to the (020), (110), (120), (111), (150), (002), and (081) crystal planes, respectively. , When the Mn/Mo ratio was 1/1, the diffractions of MnMoO 4 (JCPDS-72-0285) at 22.7, 25.8, 26.7, 31.3, 33.0, 42.5, 46.4, and 51.2° were detected, which were attributed to the (021), (220), (−112), (112), (−222), (−241), (042), and (−204) crystal planes, respectively. At the Mn/Mo ratios of 1/2, the emergence of diffraction peaks was attributed to MoO 3 , while MnO 2 (JCPDS-24-0735) and Mn 2 O 3 phases were detected when Mn was in excess. Notably, the peak intensities corresponding to MnO 2 at 37.3, 56.6, 64.8, and 72.2° corresponding to the (101), (211), (002), and (301) crystal planes increased with the increases in Mn/Mo ratios, indicating the generation of Mn species with higher oxidation states.…”
Section: Resultssupporting
confidence: 76%
“…X-ray diffraction (XRD) patterns were then used to present the phase component of the catalysts. As illustrated in Figure a, the diffraction peaks of the neat Mn- or Mo-based oxide were in good accordance with the standard patterns of Mn 2 O 3 (JCPDS-71-0636) at 23.1, 32.9, 38.2, 45.1, 49.3, 55.1, and 65.7° corresponding to the (211), (222), (400), (332), (431), and (440) crystal planes and those of MoO 3 (JCPDS-99-0080) at 12.8, 23.3, 25.9, 27.3, 33.7, 40.0, 49.2, and 58.8° corresponding to the (020), (110), (120), (111), (150), (002), and (081) crystal planes, respectively. , When the Mn/Mo ratio was 1/1, the diffractions of MnMoO 4 (JCPDS-72-0285) at 22.7, 25.8, 26.7, 31.3, 33.0, 42.5, 46.4, and 51.2° were detected, which were attributed to the (021), (220), (−112), (112), (−222), (−241), (042), and (−204) crystal planes, respectively. At the Mn/Mo ratios of 1/2, the emergence of diffraction peaks was attributed to MoO 3 , while MnO 2 (JCPDS-24-0735) and Mn 2 O 3 phases were detected when Mn was in excess. Notably, the peak intensities corresponding to MnO 2 at 37.3, 56.6, 64.8, and 72.2° corresponding to the (101), (211), (002), and (301) crystal planes increased with the increases in Mn/Mo ratios, indicating the generation of Mn species with higher oxidation states.…”
Section: Resultssupporting
confidence: 76%
“…Concerning the synthetic routes, there are many reports on the preparation of MnMoO 4 . These materials have been produced by the solid-state ceramic route, , combustion synthesis, precipitation, sonochemical, ,, microemulsion-based method, , ultralow temperature, solvent-free microwave, and hydrothermal technology. ,,, In this respect, the hydrothermal technology appears as the most powerful synthesis methodology to produce single-phase, crystalline materials . This technology make use of solubilization/precipitation phenomena shared with redox and acid–base chemistry, which allow the assessment to new hybrid inorganic/organic compounds.…”
Section: Introductionmentioning
confidence: 99%
“…The product was fabricated by a facile two-step hydrothermal route based on previous articles. First, a copper mesh (400 mesh, 8 × 8 cm 2 ) was ultrasonically cleaned for 15 min in acetone, ethanol, and deionized water. The MnCO 3 -coated mesh was synthesized by a hydrothermal route: 0.0125 mol of MnCl 2 ·4H 2 O and 0.0125 mol of sodium citrate were dissolved in 100 mL of deionized water, and the solution was stirred for 30 min.…”
Section: Methodsmentioning
confidence: 99%