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  • 1
    UID:
    gbv_1821573153
    ISSN: 0169-4332
    Content: Semiconductors have been modulated in thickness to optimize their surface-enhanced Raman scattering (SERS) activity in noble metal/semiconductor SERS substrates. However, the charge transfer (CT) resonance mechanism caused by the change of the semiconductor thickness has not been fully clarified yet, due to the influence of the strong surface plasmon resonance (SPR) effect from the noble metals. Here, systems of p-aminothiophenol (PATP) molecules chemisorbed on TiO2/Ni nanopillar array films with precisely controlled TiO2 thicknesses (PATP/TiO2/Ni) were developed to systematically evaluate the TiO2 thickness-dependent CT mechanism on the premise of minimizing the SPR influence. Ultraviolet-visible, photoluminescence and X-ray photoelectron spectroscopy results demonstrated that four parts that ascribed to the SERS enhancement, photo-induced CT from Ni to TiO2, resonance excitation of TiO2, CT from TiO2 surface states to PATP molecules, and the molecular resonance of PATP molecules, are highly TiO2-thickness dependent. Hence the whole system exhibits a strong TiO2-thickness-dependent CT effect (at the two interfaces of Ni-TiO2 and TiO2-PATP) and SERS activity with a maximum SERS intensity at a TiO2 thickness of 40 nm. This work shall be valuable for future developing an optimal metal/semiconductor SERS substrates and obtaining an in-depth understanding of the semiconductor-thickness-dependent charge transfer mechanism for SERS applications.
    In: Applied surface science, Amsterdam [u.a.] : Elsevier, 1985, 610(2023) vom: 1. Feb., Artikel-ID 155573, 0169-4332
    In: volume:610
    In: year:2023
    In: day:1
    In: month:02
    In: elocationid:155573
    Language: English
    Author information: Lei, Yong
    Author information: Zhao, Huaping
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    UID:
    gbv_1821573056
    Content: Semiconductors have been modulated in thickness to optimize their surface-enhanced Raman scattering (SERS) activity in noble metal/semiconductor SERS substrates. However, the charge transfer (CT) resonance mechanism caused by the change of the semiconductor thickness has not been fully clarified yet, due to the influence of the strong surface plasmon resonance (SPR) effect from the noble metals. Here, systems of p-aminothiophenol (PATP) molecules chemisorbed on TiO2/Ni nanopillar array films with precisely controlled TiO2 thicknesses (PATP/TiO2/Ni) were developed to systematically evaluate the TiO2 thickness-dependent CT mechanism on the premise of minimizing the SPR influence. Ultraviolet-visible, photoluminescence and X-ray photoelectron spectroscopy results demonstrated that four parts that ascribed to the SERS enhancement, photo-induced CT from Ni to TiO2, resonance excitation of TiO2, CT from TiO2 surface states to PATP molecules, and the molecular resonance of PATP molecules, are highly TiO2-thickness dependent. Hence the whole system exhibits a strong TiO2-thickness-dependent CT effect (at the two interfaces of Ni-TiO2 and TiO2-PATP) and SERS activity with a maximum SERS intensity at a TiO2 thickness of 40 nm. This work shall be valuable for future developing an optimal metal/semiconductor SERS substrates and obtaining an in-depth understanding of the semiconductor-thickness-dependent charge transfer mechanism for SERS applications.
    In: Applied surface science, Amsterdam : Elsevier, 1985, 610(2023) vom: 1. Feb., Artikel-ID 155573
    In: volume:610
    In: year:2023
    In: day:1
    In: month:02
    In: elocationid:155573
    Language: English
    URL: Volltext  (lizenzpflichtig)
    Author information: Lei, Yong
    Author information: Zhao, Huaping
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    UID:
    gbv_1771305606
    Format: 9
    ISSN: 0009-2509
    Content: Nanostructured current collectors have larger specific surface area and short ion/electron transport path, which are highly desirable for supercapacitors applications. Herein, Co0.85SeNiNPs (Co0.85Se@NiNP) hybrid electrodes are proposed and fabricated, in which NiNP is served as nanostructured current collectors. NiNP has a vertical pore structure and a large specific surface area, which could effectively promote the ion/electron transport efficiency and reduce internal electrical resistance. Compared with Ni foam and Ni foil as current collectors, NiNP enables Co0.85Se@NiNP electrodes show significantly improved specific capacity, rate performance and cycle stability. Finally, an asymmetric supercapacitor device was assembled with Co0.85Se@NiNP hybrid electrode as the binder-free positive electrode and activated carbon (AC) coated on nickel foam as negative electrode. The Co0.85Se@NiNP//AC asymmetric supercapacitors can work in a wide potential window of 0 - 1.6 V with an ultrahigh specific capacity of 182.3 F g^-1 at 1 A g^-1. Most importantly, Co0.85Se@NiNP//AC has a high energy density of 64.81 Wh kg^-1 at 800 W kg^-1 and an outstanding cycle stability of up to 12000 cycles, indicating that Co0.85Se@NiNP electrode has great application potential in supercapacitors.
    In: Chemical engineering science, Amsterdam : Elsevier, 1951, Volume 247 (2022), 117081, Seite 1-9, 0009-2509
    In: volume:247
    In: year:2022
    In: pages:117081
    In: extent:9
    Language: English
    Author information: Lei, Yong
    Author information: Zhao, Huaping
    Library Location Call Number Volume/Issue/Year Availability
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