The catalytic active sites in partially reduced MoO3 for the hydroisomerization of 1-pentene and n-pentane

Modulating the Electrocatalytic Performance of Palladium with the Electronic Metal–Support Interaction: A Case Study on Oxygen Evolution Reaction

“…Besides, no other metal is found, especially for the contaminative Fe in the as-prepared WO 3 and MoO 3 films (Figure S6). From the core level XPS spectra of Fe 2p, W 4f, and Mo 3d in Figure S7, dominant states of Fe 3+ , W 6+ , and Mo 6+ can be recognized, according to the BE peaks at 710.9 eV (Fe 2p 3/2 ), 35.6 eV (W 4f 7/2 ), and 232.6 eV (Mo 3d 5/2 ), respectively.…”

“…Figure 2a S6). From the core level XPS spectra of Fe 2p, W 4f, and Mo 3d in Figure S7, dominant states of Fe 3+ , W 6+ , and Mo 6+ can be recognized, according to the BE peaks at 710.9 eV (Fe 2p 3/2 ), 44 35.6 eV (W 4f 7/2 ), 45 and 232.6 eV (Mo 3d 5/2 ), 46 respectively. The core level XPS spectra of Pd 3d in metal-oxide/Pd catalysts are displayed in Figure 2c together with those in metallic Pd, Pd-250, Pd-350, and Pd-450.…”

Enhancement of electrochemical and catalytic properties of MoS2 through ball-milling

“…However, after the milling process more signals were recorded accounting for the presence of other elements such as Mg, Si, Ca, Fe and Cu and with an increased oxygen content ( Figure 1E). Mo 5+ and Mo 6+ [15,16] as a result of an oxidative process occurring during the ball-milling. This is also supported by the higher content of oxygen as depicted in Figure 1A and 2A.…”

Simultaneous Removal of Elemental Mercury and NO from Simulated Flue Gas at Low Temperatures over Mn–V–W/TiO2 Catalysts

“…W 4f could be divided into W 4f 7/2 peaks with a binding energy of 35.6 eV and W 4f 5/2 peaks with a binding energy of 37.40 eV, both of which corresponded to WO 3 . 49 This means that W always existed in the catalyst in the form of WO 3 , independent of calcination temperature.…”