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Third-generation photovoltaic materials, including metal halide perovskites (MHPs), colloidal quantum dots (QDs), copper zinc tin sulfide (CZTS), and organic semiconductors, among others, have become attractive in the past two decades. Unlike their first- and second-generation counterparts, these advanced materials boast properties beyond mere photovoltaic performance, such as mechanical flexibility, light weight, and cost-effectiveness. Meanwhile, these materials possess more intricate crystalline structures that aid in understanding and predicting their transport properties. In particular, the distinctive phonon dispersions in MHPs, the layered architecture in quasi-two-dimensional (2D) perovskites, the strong quantum confinement in QDs, and the complex crystal structures interspersed with abundant disorders in quaternary CZTS result in unique and sometimes anomalous thermal transport behaviors. Concurrently, the criticality of thermal management in applications such as photovoltaics, thermoelectrics, light emitting diodes, and photodetection devices has received increased recognition, considering that many of these third-generation photovoltaic materials are not good thermal conductors. Effective thermal management necessitates precise measurement, advanced modeling, and a profound understanding and interpretation of thermal transport properties in these novel materials. In this review, we provide a comprehensive summary of various techniques for measuring thermal transport properties of these materials and discuss the ultralow thermal conductivities of three-dimensional (3D) MHPs, superlattice-like thermal transport in 2D perovskites, and novel thermal transport characteristics inherent in QDs and CZTS. By collecting and comparing the literature-reported results, we offer a thorough discussion on the thermal transport phenomenon in these materials. The collective understanding from the literature in this area, as reviewed in this article, can provide guidance for improving thermal management across a wide spectrum of applications extending beyond photovoltaics. 

The detection of mid-infrared (MIR) light is technologically important for applications such as night vision, imaging, sensing, and thermal metrology. Traditional MIR photodetectors either require cryogenic cooling or have sophisticated device structures involving complex nanofabrication. Here, we conceive spectrally tunable MIR detection by using two-dimensional metal halide perovskites (2D-MHPs) as the critical building block. Leveraging the ultralow cross-plane thermal conductivity and strong temperature-dependent excitonic resonances of 2D-MHPs, we demonstrate ambient-temperature, all-optical detection of MIR light with sensitivity down to 1 nanowatt per square micrometer, using plastic substrates. Through the adoption of membrane-based structures and a photonic enhancement strategy unique to our all-optical detection modality, we further improved the sensitivity to sub–10 picowatt-per-square-micrometer levels. The detection covers the mid-wave infrared regime from 2 to 4.5 micrometers and extends to the long-wave infrared wavelength at 10.6 micrometers, with wavelength-independent sensitivity response. Our work opens a pathway to alternative types of solution-processable, long-wavelength thermal detectors for molecular sensing, environmental monitoring, and thermal imaging. 

In recent years, optical pump-probe microscopy (PPM) has become a vital technique for spatiotemporally imaging electronic excitations and charge-carrier transport in metals and semiconductors. However, existing methods are limited by mechanical delay lines with a probe time window of only several nanoseconds (ns), or monochromatic pump and probe sources with restricted spectral coverage and temporal resolution, hindering their amenability in studying relatively slow processes. To bridge these gaps, we introduce a dual-hyperspectral PPM setup with a time window spanning from ns to milliseconds and single-ns resolution. Our method features a wide-field probe tunable from 370 nm to 1000 nm and a pump spanning from 330 nm to 16 µm. We apply this PPM technique to study various two-dimensional metal-halide perovskites (2D-MHPs) as representative semiconductors by imaging their transient responses near the exciton resonances under both above-bandgap, electronic pump excitation, and below-bandgap, vibrational pump excitation. The resulting spatially- and temporally-resolved images reveal insights into heat dissipation, film uniformity, distribution of impurity phases, and film-substrate interfaces. In addition, the single-ns temporal resolution enables the imaging of in-plane strain wave propagation in 2D-MHP single crystals. Our method, which offers extensive spectral tunability and significantly improved time resolution, opens new possibilities for the imaging of charge carriers, heat, and transient phase transformation processes, particularly in materials with spatially-varying composition, strain, crystalline structure, and interfaces.