All-Vacuum-Deposited Lead-Free Perovskite Films for Charge-Transfer-Assisted SERS Substrates
Yi-Kai Chen a,  b, Shin-Han Huang b,  c, Chih-Chien Lee a, Yu-Ching Huang b,  d, Shun-Wei Liu b,  c
a Department of Electronic Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan
b Organic Electronics Research Center, Ming Chi University of Technology, New Taipei City 24031, Taiwan
c College of Engineering, Ming Chi University of Technology, New Taipei City 243303, Taiwan
d Department of Materials Engineering, Ming Chi University of Technology, New Taipei City 24031, Taiwan
Oral, Yi-Kai Chen, presentation 041
Publication date: 22nd October 2026

Lead-based perovskites have attracted considerable attention for surface-enhanced Raman scattering (SERS) applications owing to their tunable band structures and favorable optoelectronic properties. However, their intrinsic toxicity and associated environmental concerns remain major barriers to practical implementation. To address these challenges, we present lead-free cesium bismuth halide perovskite/Ag hybrid SERS substrates prepared by thermal co-evaporation of CsBr and BiI3 followed by Ag deposition.
     To achieve comparable SERS performance with a more controllable architecture, we developed bilayer structures and systematically tuned their layer thickness ratio and stacking sequence. The incorporation of the lead-free perovskite layer is expected to establish favorable energy-level alignment and facilitate interfacial charge-transfer interactions between the substrate and adsorbed molecules. Such interactions can contribute additional chemical enhancement (CM), which, together with the localized electromagnetic enhancement (EM) originating from Ag nanostructures, leads to amplified Raman responses of target analytes, enabling highly sensitive molecular detection. Rhodamine 6G (R6G) was employed as a probe molecule to evaluate SERS performance. Compared with bare Ag substrates, the lead-free perovskite/Ag substrate exhibited significantly enhanced Raman signals at characteristic peaks of 612, 774, 1362, and 1650 cm-1. Concentration-dependent measurements revealed a limit of detection (LOD) down to 10-7 M. Beyond R6G, the perovskite interlayer extended detection to Thiabendazole (TBZ), which shows no signal on bare Ag, down to 10-7 M. These findings highlight all-vacuum-deposited lead-free perovskite films as scalable, environmentally friendly, charge-transfer-assisted SERS platforms, and show that a rationally designed bilayer can match co-evaporated films while offering precise control for high-sensitivity molecular sensing.

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