2021
DOI: 10.1016/s1872-2067(20)63669-5
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Highly dispersed boron-nitride/CuO -supported Au nanoparticles for catalytic CO oxidation at low temperatures

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Cited by 14 publications
(12 citation statements)
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“…[28] The chemical structure of the prepared nanofiber catalysts before and after calcination was investigated by FT-IR spectroscopy (Figure 3a). The band observed at 3412 cm À 1 for the uncalcined nanofiber catalyst was attributed to the stretching vibrations of SiÀ OH [32] or BÀ OH [33] bond, and band at 1210 cm À 1 was ascribed to the stretching vibration of BÀ O bond. [10] Due to the interference of the stretching vibrations of SiÀ OH group, it was difficult to confirm the BÀ OH in the nanofiber catalyst.…”
Section: Design and Structure Characterization Of H-bn/sio 2 Nanofibersmentioning
confidence: 97%
See 1 more Smart Citation
“…[28] The chemical structure of the prepared nanofiber catalysts before and after calcination was investigated by FT-IR spectroscopy (Figure 3a). The band observed at 3412 cm À 1 for the uncalcined nanofiber catalyst was attributed to the stretching vibrations of SiÀ OH [32] or BÀ OH [33] bond, and band at 1210 cm À 1 was ascribed to the stretching vibration of BÀ O bond. [10] Due to the interference of the stretching vibrations of SiÀ OH group, it was difficult to confirm the BÀ OH in the nanofiber catalyst.…”
Section: Design and Structure Characterization Of H-bn/sio 2 Nanofibersmentioning
confidence: 97%
“…[10] Due to the interference of the stretching vibrations of SiÀ OH group, it was difficult to confirm the BÀ OH in the nanofiber catalyst. However, the presence of BÀ OH [33] (3394 cm À 1 ) was observed for the exfoliated h-BN by ball-milling (Figure 3b). According to the above experimental results, we speculated that the existence of BÀ OH species over the h-BN/SiO 2 nanofiber catalyst.…”
Section: Design and Structure Characterization Of H-bn/sio 2 Nanofibersmentioning
confidence: 98%
“…The h ‐BN was processed by planetary ball‐milling (Pulverisette 7, Fritsch) at 800 r/min for 15 min at room temperature and then washed for 2 h with deionized water at 80 o C. [ 34‐35 ] Subsequently, the wet sample was suction‐filtered and dried in an oven at 50 o C for 12 h. In this way, the obtained sample was named BN.…”
Section: Methodsmentioning
confidence: 99%
“…that give BN the potential to be used in many applications. In recent years, BN has demonstrated its great potential in optics (optoelectronic devices and detectors), electrochemistry (electrochemical sensor platforms and biocompatibility), catalysis, and detection (temperature sensing, gas sensing, and humidity sensing). …”
Section: Introductionmentioning
confidence: 99%