2009
DOI: 10.1016/j.susc.2009.07.006
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SEM and XPS studies of nanohole arrays on InP(100) surfaces created by coupling AAO templates and low energy Ar+ ion sputtering

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Cited by 10 publications
(10 citation statements)
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“…A peak appeared at 134.5 eV for S1, which originated from the oxidized state of P atoms. 12 This indicated the oxidization of InP substrate took place, which was consistent with XRR analysis. Al 2p peak located at 74.1 eV for S1 but it shifted down to 73.9eV for S2.…”
supporting
confidence: 81%
“…A peak appeared at 134.5 eV for S1, which originated from the oxidized state of P atoms. 12 This indicated the oxidization of InP substrate took place, which was consistent with XRR analysis. Al 2p peak located at 74.1 eV for S1 but it shifted down to 73.9eV for S2.…”
supporting
confidence: 81%
“…37 − 40 For our In 4d measurements shown in Figure 4 a–c(ii), we observe a small component (orange) shifted to 0.6 eV higher binding energy than the bulk component (blue), which may arise from an oxide component. 41 43 However, we can also see an additional component at 0.75 eV lower binding energy in the In 4d spectra (red), principally on the upper end of the nanowire (n-doped region). This may indicate the presence of metallic In or some In/Au alloy species 43 either arising from the In enriched Au particle at the top of the nanowire 25 or some alloying of the In of the NW with the Au-covered electrodes.…”
mentioning
confidence: 95%
“…Porous AAO was used as the catalyst support; it was prepared by anodization of aluminum sheet using aqueous oxalic acid solution [50][51][52][53]. Briefly, a high purity aluminum foil was anodized …”
Section: Preparation Of Aao Support and Nio-ceo2/aao Catalystmentioning
confidence: 99%
“…Porous AAO was used as the catalyst support; it was prepared by anodization of aluminum sheet using aqueous oxalic acid solution [50][51][52][53]. Briefly, a high purity aluminum foil was anodized in the oxalic acid solution of 0.3 M at 40 V for 24 h at a temperature of 10 • C to form a porous γ-Al 2 O 3 layer, and then, pore widening treatment was performed with the same aqueous oxalic acid solution mentioned above for 4 h at 30 • C. When the pore widening treatment was finished, it was immersed in deionized water for sufficient time to wash out the residual oxalic acid.…”
Section: Preparation Of Aao Support and Nio-ceo 2 /Aao Catalystmentioning
confidence: 99%