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Ti–Si–Zr–Zn Nanometallic Glass Substrate with a Tunable Zinc Composition for Surface-Enhanced Raman Scattering of Cytochrome c
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Number of Authors: 82023 (English)In: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 15, no 21, p. 25275-25284Article in journal (Refereed) Published
Abstract [en]

As a remarkably powerful analytical technique, surface-enhanced Raman scattering (SERS) continues to find applications from molecular biology and chemistry to environmental and food sciences. In search of reliable and affordable SERS substrates, the development has moved from noble metals to other diverse types of structures, e.g., nano-engineered semiconductor materials, but the cost of the enhancement factors (EF) substantially decreasing. In this work, we employ biocompatible thin films of Ti–Si–Zr–Zn nanometallic glasses as the SERS substrates, while tuning the Zn composition. Aided by quartz crystal microbalance, we find that the composition of 4.3% Zn (Ti–Si–Zr–Zn4.3) gives an ultrasensitive detection of Cytochrome c (Cyt c) with an EF of 1.38 × 104, 10-fold higher than the previously reported EF in the semiconducting metal oxide nanomaterials, such as TiO2, and even comparable to the reported noble-metal-assisted semiconducting tungsten oxide hydrate. Ti–Si–Zr–Zn4.3 exhibits a stronger adhesion force toward Cyt c, which ensures the strong binding of Cyt c to the surface, facilitating the Cyt c adsorption onto the surface and thus enhancing the SERS signal. The high separation efficiency of photoinduced electrons and holes in Ti–Si–Zr–Zn4.3 is also acknowledged for promoting the SERS activity. 

Place, publisher, year, edition, pages
2023. Vol. 15, no 21, p. 25275-25284
Keywords [en]
surface-enhanced Raman scattering, nanometallic glass, enhancement factors, ultrasensitive detection of proteins, amorphous
National Category
Analytical Chemistry Materials Chemistry
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URN: urn:nbn:se:su:diva-230077DOI: 10.1021/acsami.3c00498ISI: 001014376700001PubMedID: 37212432Scopus ID: 2-s2.0-85160964875OAI: oai:DiVA.org:su-230077DiVA, id: diva2:1867173
Available from: 2024-06-10 Created: 2024-06-10 Last updated: 2024-06-10Bibliographically approved

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Laaksonen, Aatto

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