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Ultrafast Charge Transfer 2D MoS(2)/Organic Heterojunction for Sensitive Photodetector
The 2D MoS(2) with superior optoelectronic properties such as high charge mobility and broadband photoresponse has attracted broad research interests in photodetectors (PD). However, due to the atomic thin layer of 2D MoS(2), its pure photodetectors usually suffer from inevitable drawbacks such as l...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131850/ https://www.ncbi.nlm.nih.gov/pubmed/36808857 http://dx.doi.org/10.1002/advs.202207743 |
Sumario: | The 2D MoS(2) with superior optoelectronic properties such as high charge mobility and broadband photoresponse has attracted broad research interests in photodetectors (PD). However, due to the atomic thin layer of 2D MoS(2), its pure photodetectors usually suffer from inevitable drawbacks such as large dark current, and intrinsically slow response time. Herein, a new organic material BTP‐4F with high mobility is successfully stacked with 2D MoS(2) film to form an integrated 2D MoS(2)/organic P–N heterojunction, facilitating efficient charge transfer as well as significantly suppressed dark current. As a result, the as‐obtained 2D MoS(2)/organic (PD) has exhibited excellent response and fast response time of 332/274 µs. The analysis validated photogenerated electron transition from this monolayer MoS(2) to subsequent BTP‐4F film, whereas the transited electron is originated from the A(−) exciton of 2D MoS(2) by temperature‐dependent photoluminescent analysis. The ultrafast charge transfer time of ≈0.24 ps measured by time‐resolved transient absorption spectrum is beneficial for efficient electron–hole pair separation, greatly contributing to the obtained fast photoresponse time of 332/274 µs. This work can open a promising window to acquire low‐cost and high‐speed (PD). |
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