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SnS2 is a two-dimensional (2D) layered semiconductor with a visible-range bandgap (~2.3eV), high charge carrier mobility, long carrier lifetimes, and good environmental stability. This study explores the impact of zero-valent metal intercalation into the van der Waals gaps of SnS2 on charge carrier dynamics. We demonstrate that metal intercalation enhances optical absorption in the yellow-to-IR range and induces metal-dependent bandgap shifts. Time-resolved THz spectroscopy reveals that different metals uniquely influence photoconductivity dynamics: We find that intercalation with Bi, Ni, and Fe shortens the photoconductivity decay times, whereas Rh intercalation results in a slower decay. These findings highlight the potential of metal intercalation to tailor SnS2 properties for diverse applications, from solar energy conversion to high-speed photodetectors. 

Use of nanomaterials for photocatalysis faces challenges such as complex synthesis, high cost, low scalability, and dependance on UV radiation for initiating the photocatalytic activity. We recently demonstrated scalable, one-pot syntheses of one-dimensional (1D) lepidocrocite-based nanofilaments (NFs), 1DL NFs, that have the potential to overcome some of the challenges. 1DL NFs are exceptionally stable in water, have a large surface to volume ratio, and sub-square-nanometer cross sections. Initial reports show the semiconducting nature of this material, with an indirect band gap energy of 4.0 eV, one of the highest ever reported for a titania material. In this work, we present a study of the electronic and optical properties of these newly discovered 1DL NFs using ultrafast transient optical absorption. We show that despite the large band gap of this material, sub-gap states can be accessed with visible light illumination only, and photoexcited species reveal decay times in the nanosecond scale. Long lived photoexcitations in the visible range, without assistance by UV illumination, pave the way for possible application in photocatalysis. 

The advent of dispersion-engineered and highly nonlinear nanophotonics is expected to open up an all-optical path towards the strong-interaction regime of quantum optics by combining high transverse field confinement with ultra-short-pulse operation. Obtaining a full understanding of photon dynamics in such broadband devices, however, poses major challenges in the modeling and simulation of multimode non-Gaussian quantum physics, highlighting the need for sophisticated reduced models that facilitate efficient numerical study while providing useful physical insight. In this manuscript, we review our recent efforts in modeling broadband optical systems at varying levels of abstraction and generality, ranging from multimode extensions of quantum input-output theory for sync-pumped oscillators to the development of numerical methods based on a field-theoretic description of nonlinear waveguides. We expect our work not only to guide ongoing theoretical and experimental efforts towards next-generation quantum devices but also to uncover essential physics of broadband quantum photonics.