Abstract
Nanoparticle films are ubiquitous thermal and electrocatalysts, yet their \textit{operando} characterization remains challenging. Vibrational sum-frequency generation (vSFG) spectroscopy offers unique advantages due to its high sensitivity and surface specificity, but its application to systems with such intermediate length scale disorder, particularly with phase-resolved detection, has been challenging. In this study, we describe an approach to phase-resolved vSFG spectroscopy of nanoparticle films using z-cut $\alpha$-quartz as a local reference. We show, by analysis of an octadecyltrichlorosilane (OTS) film on quartz under the \textit{ppp} polarization condition, quantitative detection of absolute phase is possible and subsequently apply this protocol to a film of Mn-doped \ch{Co3O4} nanoparticles. Two OH species are resolved ($\sim 3585$ and $\sim 3770~\text{cm}^{-1}$), both oriented H-up relative to the surface. This approach delivers a practical, internally referenced, phase-resolved vSFG methodology for nanoparticle ensembles on dielectric supports, and thus offers \textit{operando} access to catalytic interfaces beyond metallic or plasmonically enhanced systems.
Supplementary materials
Title
Supporting Information for ”Characterization of Nanoparticulate Films Using Phase Sensitive Vibrational Sum Frequency Spectroscopy”
Description
SEM, size distribution, XRD of the NPs; Sample preparation details; Details of vSFG measurements; Scheme of the eight-degree-of-freedom sample stage; Detailed theory of the phase-resolved vSFG; Parameters used to calculate the signs in Table I; Azimuthal dependent vSFG field and intensity; Typical shapes of azimuthal dependent pattern for NPs on z-cut quartz; vSFG results of OTS SAM-modified quartz measured under ssp/psp polarization combinations; vSFG results for NPs on quartz measured under ssp/psp polarization combinations; Fitting parameters for the two Lorentzian features of Figure 3; The UV–Vis absorbance and raw SFG spectra of the NPs.
Actions



![Author ORCID: We display the ORCID iD icon alongside authors names on our website to acknowledge that the ORCiD has been authenticated when entered by the user. To view the users ORCiD record click the icon. [opens in a new tab]](https://www.cambridge.org/engage/assets/public/coe/logo/orcid.png)