Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, UK.
Nanoscale. 2019 Mar 14;11(11):4726-4734. doi: 10.1039/c8nr07655c.
Monolayered, semiconducting molybdenum disulfide (MoS2) is of considerable interest for its potential applications in next-generation flexible, wearable, and transparent photodetectors because it has outstanding physical properties coupled with unique atomically thin dimensions. However, there is still a lack of understanding in terms of the underlying mechanisms responsible for the photoresponse dynamics, which makes it difficult to identify the appropriate device design strategy for achieving a fast photoresponse time in MoS2 photodetectors. In this study, we investigate the importance of surface functionalization on controlling the charge carrier densities in a MoS2 monolayer and in turn the corresponding behavior of the photoresponse in relation to the position of the Fermi-level and the energy band structure. We find that the p-doping and n-doping, which is achieved through the surface functionalization of the MoS2 monolayer, leads to devices with different photoresponse behavior. Specifically, the MoS2 devices with surface functional groups contributing to p-doping exhibited a faster response time as well as higher sensitivity compared to that observed for the MoS2 devices with surface functional groups contributing to n-doping. We attribute this difference to the degree of bending in the energy bands at the metal-semiconductor junction as a result of shifting in the Fermi-level position, which influences the optoelectronic transport properties as well as the recombination dynamics leading to a low dark and thus high detectivity and fast decay time. Based upon these findings, we have also demonstrated the broad applicability of surface functionalization by fabricating a flexible MoS2 photodetector that shows an outstanding decay time of 0.7 s, which is the fastest response time observed in flexible MoS2 detectors ever reported.
单层、半导体二硫化钼 (MoS2) 因其在下一代柔性、可穿戴和透明光电探测器中的潜在应用而受到极大关注,因为它具有出色的物理特性,同时具有独特的原子级厚度。然而,对于光响应动力学的潜在机制,人们仍然缺乏了解,这使得难以确定适当的器件设计策略,以实现 MoS2 光电探测器的快速光响应时间。在这项研究中,我们研究了表面功能化对控制 MoS2 单层中的电荷载流子密度的重要性,以及相应的光响应行为与费米能级和能带结构位置的关系。我们发现,通过 MoS2 单层的表面功能化实现的 p 型掺杂和 n 型掺杂导致器件具有不同的光响应行为。具体来说,与表面功能基团贡献 n 型掺杂的 MoS2 器件相比,表面功能基团贡献 p 型掺杂的 MoS2 器件具有更快的响应时间和更高的灵敏度。我们将这种差异归因于费米能级位置移动导致金属-半导体结能带弯曲程度的不同,这会影响光电输运特性以及导致低暗电流的复合动力学,从而实现高探测率和快速衰减时间。基于这些发现,我们还通过制造具有出色 0.7 s 衰减时间的柔性 MoS2 光电探测器,展示了表面功能化的广泛适用性,这是迄今为止报道的柔性 MoS2 探测器中最快的响应时间。