双金属片
材料科学
多孔硅
贵金属
成核
电化学
沉积(地质)
化学工程
硅
金属
纳米颗粒
拉曼光谱
X射线光电子能谱
多孔性
胶体金
蚀刻(微加工)
电极
纳米技术
薄膜
化学气相沉积
表面增强拉曼光谱
纳米结构
作者
Chia-Chi Lu,Hsien-Yü Hsü,I-An Lin,Vincent K. S. Hsiao,Chih-Chien Chu
标识
DOI:10.1021/acsmaterialsau.5c00169
摘要
This study presents a one-step electrochemical etching strategy that enables the simultaneous formation of porous silicon (PSi) and in situ deposition of noble metal nanoparticles (NPs), which subsequently act as nucleation sites for gold growth to form bimetallic SERS substrates. Three metal precursors─K2PtCl4, HAuCl4, and K2PdCl4─were systematically compared to elucidate how precursor type affects PSi morphology, nanoparticle distribution, and subsequent gold deposition. SEM and EDS analyses revealed distinct deposition behaviors among the metals, leading to varied gold nucleation efficiencies and SERS enhancement levels. HAuCl4-treated substrates produced the highest absolute Raman intensity, while K2PtCl4-treated substrates exhibited lower intensity but superior spectral quality with minimal fluorescence background and sharper peaks. XRD and XPS confirmed successful gold deposition and precursor-dependent interfacial interactions, including the formation of Pt–Au bimetallic interfaces. Reusability tests demonstrated that the Pt-assisted substrates maintained stable performance over multiple cycles, confirming their structural robustness and practical feasibility. Overall, this work provides mechanistic insight into how noble metal interfaces govern SERS spectral characteristics and establishes a rational pathway for designing PSi-based SERS substrates emphasizing spectral precision, reproducibility, and reusability rather than mere sensitivity enhancement.
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