Ultra-broadband detection by photovoltaic and thermoelectric coupling based on large-scale single-crystalline SnSe thin film

Recently, the layered tin selenide (SnSe) has attracted intense attention from the researchers due to its distinguished thermoelectric properties, thus giving this compound quite a promising potential application for photothermoelectric detectors. However, the low-cost epitaxial growth method toward...

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Veröffentlicht in:Applied physics letters 2024-12, Vol.125 (23)
Hauptverfasser: Zhang, Xianjing, Liu, Fengliang, Wan, Yu, Guo, Bowen, Wang, Qisheng
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Sprache:eng
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Zusammenfassung:Recently, the layered tin selenide (SnSe) has attracted intense attention from the researchers due to its distinguished thermoelectric properties, thus giving this compound quite a promising potential application for photothermoelectric detectors. However, the low-cost epitaxial growth method toward a millimeter scale single phase SnSe thin film is still rarely reported, thus limiting its fabrications in arraying photoelectric sensors. Here, we synthesized a large-scale SnSe thin film on the SrTiO3 substrate by using the crack of PbS thin film-assisted nucleation in the chemical vapor deposition, achieving a homogeneous single-crystal SnSe thin film with a centimeter scale, as revealed by the x-ray diffraction and scanning electron microscope measurement. In addition, a two-terminal device is fabricated to study the photoelectric properties of this film. Surprisingly, this SnSe detector shows a synergetic photovoltaic and thermoelectric effect, achieving an ultrabroad band detection ranging from visible (405 nm) to mid-infrared (10.0  μm) at room temperature. Significantly, this detector also shows an impressive performance with an optimized response time of 2.81 ms (at 4.0  μm), a responsivity of 290.9  V W−1 (at 4.0  μm), and a detectivity of 5.5×108 Jones (at 4.0  μm). The above results addressed the bottleneck in SnSe film synthesis, and accelerated its applications in future high-performance photoelectronic devices.
ISSN:0003-6951
1077-3118
DOI:10.1063/5.0238951