Raman and IR Signatures of Mo3S4 and Mo3S13 Molybdenum Sulphide Molecular Catalysts for Solar Hydrogen Evolution

TL;DR

This study provides detailed Raman and IR vibrational signatures of Mo3S4 and Mo3S13 molybdenum sulfide clusters, supporting their use in catalysis and energy conversion, with DFT validation and enhanced detection methods.

Contribution

It offers the first comprehensive vibrational characterization of Mo3S4 and Mo3S13 clusters using combined experimental and theoretical approaches.

Findings

Raman spectra identify key vibrational modes for both clusters.

IR spectra complement Raman data, providing complete vibrational fingerprints.

Raman spectroscopy is more sensitive than XRD for detecting these clusters.

Abstract

Molybdenum sulfide clusters, [Mo3S4]4+ and [Mo3S13]2-, have emerged as key molecular models for understanding active sites in Mo-S-based catalysts and as promising candidates for energy conversion applications. Despite their importance, comprehensive vibrational characterization of these clusters remains limited. Here, we present a detailed Raman and infrared spectroscopic analysis of both clusters, supported by density functional theory (DFT) calculations. High-quality crystalline samples were synthesized and characterized using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX) to confirm morphology and stoichiometry. Raman spectra, acquired using 488 nm and 532 nm laser excitation, were deconvoluted using Lorentzian fitting. Vibrational mode assignments were made through direct comparison with DFT predictions. For [Mo3S4]4+, major Raman bands appear near 200 cm^-1, 350 cm^-1, and 450 cm^-1, corresponding to Mo-S-Mo bending, Mo-S stretching, and terminal sulfur vibrations. [Mo3S13]2- shows two distinct spectral regions: 100-400 cm^-1 for Mo-S and S-S bending and stretching, and 450-550 cm^-1 for terminal disulfide (S-S) stretching. Complementary IR spectra calculations reveal additional vibrational features, yielding a more complete fingerprint for each cluster. Finally, we demonstrate that Raman spectroscopy offers greater sensitivity than X-ray diffraction (XRD) in detecting these clusters on supporting materials. This work provides a detailed vibrational reference for [Mo3S4]4+ and [Mo3S13]2-, establishing Raman and IR spectroscopy as powerful tools for characterizing Mo-S molecular clusters in both fundamental and applied contexts.