Higher-energy excitation at the C-exciton resonance accelerates interlayer hole transfer in WS2-graphene by opening an additional efficient channel enabled by elevated carrier temperatures.
Picosecond photoresponse in van der Waals heterostructures
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abstract
Two-dimensional (2D) crystals, such as graphene and transition metal dichalcogenides (TMDs), present a collection of unique and complementary optoelectronic properties. Assembling different 2D materials in vertical heterostructures enables the combination of these properties in one device, thus creating multi-functional optoelectronic systems with superior performance. Here we demonstrate that graphene/WSe2/graphene heterostructures ally the high photodetection efficiency of TMDs with a picosecond photoresponse comparable to that of graphene, thereby optimizing both speed and efficiency in a single photodetector. We follow in time the extraction of photoexcited carriers in these devices using time-resolved photocurrent measurements and demonstrate a photoresponse time as short as 5.5 ps, which we tune by applying a bias and by varying the TMD layer thickness. Our study provides direct insight into the physical processes governing the detection speed and quantum efficiency of these van der Waals (vdW) heterostuctures, such as out-of-plane carrier drift and recombination. The observation and understanding of ultrafast and efficient photodetection demonstrate the potential of hybrid TMD-based heterostructures as a platform for future optoelectronic devices.
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cond-mat.mes-hall 1years
2025 1verdicts
UNVERDICTED 1representative citing papers
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Influence of excitation energy on microscopic quantum pathways for ultrafast charge transfer in van der Waals heterostructures
Higher-energy excitation at the C-exciton resonance accelerates interlayer hole transfer in WS2-graphene by opening an additional efficient channel enabled by elevated carrier temperatures.