Kozbial Andrew, Gong Xiao, Liu Haitao, Li Lei
‡Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.
Langmuir. 2015 Aug 4;31(30):8429-35. doi: 10.1021/acs.langmuir.5b02057. Epub 2015 Jul 22.
2D semiconductors allow for unique and ultrasensitive devices to be fabricated for applications ranging from clinical diagnosis instruments to low-energy light-emitting diodes (LEDs). Graphene has championed research in this field since it was first fabricated; however, its zero bandgap creates many challenges. Transition metal dichalcogenides (TMDCs), e.g., MoS2, have a direct bandgap which alleviates the challenge of creating a bandgap in graphene-based devices. Water wettability of MoS2 is critical to device fabrication/performance and MoS2 has been believed to be hydrophobic. Herein, we report that water contact angle (WCA) of freshly exfoliated MoS2 shows temporal evolution with an intrinsic WCA of 69.0 ± 3.8° that increases to 89.0 ± 3.1° after 1 day exposure to ambient air. ATR-FTIR and ellipsometry show that the fresh, intrinsically mildly hydrophilic MoS2 surface adsorbs hydrocarbons from ambient air and thus becomes hydrophobic.
二维半导体能够制造出独特且超灵敏的器件,应用范围涵盖临床诊断仪器到低能发光二极管(LED)等。自首次制备以来,石墨烯一直引领着该领域的研究;然而,其零带隙带来了诸多挑战。过渡金属二硫属化物(TMDCs),例如二硫化钼(MoS2),具有直接带隙,这缓解了在基于石墨烯的器件中制造带隙的挑战。MoS2的水润湿性对器件制造/性能至关重要,并且一直被认为是疏水的。在此,我们报告新剥离的MoS2的水接触角(WCA)呈现出随时间的演变,其固有WCA为69.0±3.8°,在暴露于环境空气1天后增加到89.0±3.1°。衰减全反射傅里叶变换红外光谱(ATR-FTIR)和椭偏仪表明,新鲜的、本质上轻度亲水的MoS2表面从环境空气中吸附碳氢化合物,从而变得疏水。