The study of electronic structure of molybdenum and tungsten trisulfides and their lithium intercalates by x-ray electron and x-ray emission and absorption spectroscopy
“…Figure c shows the S 2p spectrum and the results of the deconvolution, revealing spectra corresponding to various valence states of sulfur; five sulfur environments were identified. For WS 3 and S 2p, the spectra show two partially overlapping doublets attributed to S 2− 2 pairs (on the high‐energy side) and to S 2− (on the low‐energy side) in 1:2 proportions as observed in a previous report . The singlet peak located at 164 eV was assigned to the S–S bond from elemental sulfur; the other two peaks between 169 and 170 eV are due to the presence of SO 2− 4 or SO 2− 3 , which were likely produced via the oxidation of sulfur during the hydrothermal reaction .…”
in order to restrict the loss of material. Furthermore, due to their scalability and flexibility, 3D flexible electronics (see Supporting Information (SI), where Table S1 contains a list) were considered revolutionary materials and were used in many fields such as imperceptible electronic devices, wearable electronic devices, and bionic technology. [11][12][13] Recently studies have shown the encapsulation of sulfur in the pores of carbon materials, such as meso-/microporous carbons, [11] cable-shaped carbon, [12] and carbon nanotubes/fibers, [13] can reduce the capacity fading. However, such nonpolar flexible carbon materials have a destructive disadvantage; they only have physical van der Waals (vdW) adsorption for polar Li 2 S n , which leads to the facile detachment of Li 2 S n from the carbon surface. [14] This proves that carbon-based materials alone cannot serve as the perfect host. In light of this new insight, various types of polar functional groups on carbon-based materials have been demonstrated to increase the interaction between Li 2 S n species and the electrode; these materials can generally be categorized into three types: polymers (polyaniline, polypyrrole, poly(3,4ethylenedioxythiophene) (PEDOT)), [15] metal oxides
“…Figure c shows the S 2p spectrum and the results of the deconvolution, revealing spectra corresponding to various valence states of sulfur; five sulfur environments were identified. For WS 3 and S 2p, the spectra show two partially overlapping doublets attributed to S 2− 2 pairs (on the high‐energy side) and to S 2− (on the low‐energy side) in 1:2 proportions as observed in a previous report . The singlet peak located at 164 eV was assigned to the S–S bond from elemental sulfur; the other two peaks between 169 and 170 eV are due to the presence of SO 2− 4 or SO 2− 3 , which were likely produced via the oxidation of sulfur during the hydrothermal reaction .…”
in order to restrict the loss of material. Furthermore, due to their scalability and flexibility, 3D flexible electronics (see Supporting Information (SI), where Table S1 contains a list) were considered revolutionary materials and were used in many fields such as imperceptible electronic devices, wearable electronic devices, and bionic technology. [11][12][13] Recently studies have shown the encapsulation of sulfur in the pores of carbon materials, such as meso-/microporous carbons, [11] cable-shaped carbon, [12] and carbon nanotubes/fibers, [13] can reduce the capacity fading. However, such nonpolar flexible carbon materials have a destructive disadvantage; they only have physical van der Waals (vdW) adsorption for polar Li 2 S n , which leads to the facile detachment of Li 2 S n from the carbon surface. [14] This proves that carbon-based materials alone cannot serve as the perfect host. In light of this new insight, various types of polar functional groups on carbon-based materials have been demonstrated to increase the interaction between Li 2 S n species and the electrode; these materials can generally be categorized into three types: polymers (polyaniline, polypyrrole, poly(3,4ethylenedioxythiophene) (PEDOT)), [15] metal oxides
“…MoS 3 synthesized by acidification of ATTM [34] solution is also included. This sample was prepared in order to compare the corresponding binding energies with those of the precipitated nanoparticles before reaction since the binding energy values reported in the literature vary widely [37][38][39][40][41][42][43][44][45][46][47].…”
More than half of the total world oil reserves are heavy oil, extra heavy oil, and bitumen; however their catalytic conversion to more valuable products is challenging. The use of submicronic particles or nanoparticles of catalysts suspended in the feedstock may be a viable alternative to the conversion of heavy oils at refinery level or downhole (in situ upgrading). In the present work, molybdenum sulfide (MoS2) particles with varying diameters (10000–10 nm) were prepared using polyvinylpyrrolidone as capping agent. The prepared particles were characterized by DLS, TEM, XRD, and XPS and tested in the hydrodesulfurization (HDS) of a vacuum gas oil (VGO). A correlation between particle size and activity is presented. It was found that particles with diameters around 13 nm show double the HDS activity compared with the material with micrometric particle sizes (diameter ≈ 10,000 nm).
“…Signals of W 4+ and W 5+ species are commonly observed from amorphous WS x and its derivatives [67], but the ratios of the contents are smaller in amorphous NiWS than crystalline WS x . The W 6+ peaks representing oxidation of W are more obvious in NiWS, as the precursor becomes more unstable after WS 4 2− interacts with Ni 2+ [48,67]. In the S 2p spectrum, the peaks at 162.47-162.75 and 161.37−161.65 eV correspond to the S 2p 1/2 and 2p 3/2 of S 2− ligand [38].…”
Section: Msmentioning
confidence: 99%
“…The W 4f spectra are fitted to several doublets including W 4+ 4f 5/2-7/2 , W 5+ 4f 5/2-7/2 , and W 6+ 4f 5/2-7/2 [44]. Signals of W 4+ and W 5+ species are commonly observed from amorphous WS x and its derivatives [67], but the ratios of the contents are smaller in amorphous NiWS than crystalline WS x . The W 6+ peaks representing oxidation of W are more obvious in NiWS, as the precursor becomes more unstable after WS 4 2− interacts with Ni 2+ [48,67].…”
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