Center for Nanochemistry, Beijing Science and Engineering Center for Nanocarbons, Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Peking University , Beijing 100871, P. R. China.
Academy for Advanced Interdisciplinary Studies, Peking University , Beijing 100871, P. R. China.
ACS Nano. 2016 Jul 26;10(7):6725-30. doi: 10.1021/acsnano.6b02046. Epub 2016 May 12.
Twisted bilayer graphene (tBLG) with van Hove Singularity (VHS) has exhibited novel twist-angle-dependent chemical and physical phenomena. However, scalable production of high-quality tBLG is still in its infancy, especially lacking the angle controlled preparation methods. Here, we report a facile approach to prepare tBLG with large domain sizes (>100 μm) and controlled twist angles by a clean layer-by-layer transfer of two constituent graphene monolayers. The whole process without interfacial polymer contamination in two monolayers guarantees the interlayer interaction of the π-bond electrons, which gives rise to the existence of minigaps in electronic structures and the consequent formation of VHSs in density of state. Such perturbation on band structure was directly observed by angle-resolved photoemission spectroscopy with submicrometer spatial resolution (micro-ARPES). The VHSs lead to a strong light-matter interaction and thus introduce ∼20-fold enhanced intensity of Raman G-band, which is a characteristic of high-quality tBLG. The as-prepared tBLG with strong light-matter interaction was further fabricated into high-performance photodetectors with selectively enhanced photocurrent generation (up to ∼6 times compared with monolayer in our device).
扭曲双层石墨烯(tBLG)具有范霍夫奇点(VHS),表现出新颖的转角依赖的化学和物理现象。然而,高质量 tBLG 的可扩展生产仍处于起步阶段,特别是缺乏角度可控的制备方法。在这里,我们报告了一种通过清洁的双层逐层转移两个组成石墨烯单层来制备具有大畴尺寸(>100 μm)和可控扭转角的 tBLG 的简便方法。整个过程中两层之间没有界面聚合物污染,保证了π键电子的层间相互作用,从而导致电子结构中存在微间隙和密度状态中的 VHS 形成。这种对能带结构的微扰通过具有亚微米空间分辨率(微 ARPES)的角分辨光发射谱直接观察到。VHS 导致强烈的光物质相互作用,从而引入 Raman G 带强度增强约 20 倍,这是高质量 tBLG 的特征。具有强光物质相互作用的制备好的 tBLG 进一步被制成高性能光探测器,其光电流产生选择性增强(与我们器件中的单层相比,高达约 6 倍)。