2021
DOI: 10.1016/j.nanoen.2020.105449
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Direct piezocatalytic conversion of methane into alcohols over hydroxyapatite

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Cited by 39 publications
(37 citation statements)
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“…Fig. 2c shows the PFM result of tip displacement against applied voltage for the as-prepared sample, indicating a hysteresis with butterfly shape, which is a characteristic and direct evidence of the piezoelectric response of the Bi2S3 nanorods [12,23]. 3d-f, respectively.…”
Section: Resultsmentioning
confidence: 92%
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“…Fig. 2c shows the PFM result of tip displacement against applied voltage for the as-prepared sample, indicating a hysteresis with butterfly shape, which is a characteristic and direct evidence of the piezoelectric response of the Bi2S3 nanorods [12,23]. 3d-f, respectively.…”
Section: Resultsmentioning
confidence: 92%
“…Besides the most commonly used piezoelectric materials, which are the perovskitetype structure, such as BaTiO3 [7], PbTiO3 [8], and LiNbO3 [9] that have the general formula of ABO3, other classes of materials have been investigated for piezocatalytic response. These classes encompass binary oxide [10], metal chalcogenide [11], apatite [12], and so on. Recently, Liu and collaborators reported the activity of submicrorod particles of m-Bi2O4 for the piezocatalytic degradation of sulfamethazine antibiotic [13].…”
Section: Introductionmentioning
confidence: 99%
“…In parallel, when using 3 mL H 2 16 O, 1 bar 18 O 2 and 19 bar CH 4 , the signals at m/z = 34 and 33 were attributed to the isotopic labelled CH 3 18 OH and its fragment (Figure 4d), suggesting O 2 was the only oxygen source for CH 3 OH formation. Carbon source for methanol production were also studied in the presence of 5 bar isotopic labelled 13 CH 4 (Figure 4e), where the signal of mass spectra (MS) at m/z = 33 was ascribed to 13 CH 3 OH, demonstrating that CH 4 was the carbon source for oxygenates production.…”
Section: Mechanism Investigationmentioning
confidence: 99%
“…[6][7][8] Industrial multistep route via steam reforming and subsequent Fischer-Tropsch synthesis could e ciently activate CH 4 , while it requires harsh experimental conditions (eg. > 700 o C temperature and/or high pressure), causing huge energy-consumption and safety issues [9][10][11][12][13]. In parallel, it is relatively di cult to achieve high selectivity due to the more reactive characteristics of the desired oxygenates against both the reactant CH 4 and stable product CO 2 .…”
Section: Introductionmentioning
confidence: 99%
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