Department of Chemistry, Rice University, Houston, TX 77005 (USA).
Angew Chem Int Ed Engl. 2014 Feb 3;53(6):1565-9. doi: 10.1002/anie.201306317. Epub 2014 Jan 22.
Bi- and trilayer graphene have attracted intensive interest due to their rich electronic and optical properties, which are dependent on interlayer rotations. However, the synthesis of high-quality large-size bi- and trilayer graphene single crystals still remains a challenge. Here, the synthesis of 100 μm pyramid-like hexagonal bi- and trilayer graphene single-crystal domains on Cu foils using chemical vapor deposition is reported. The as-produced graphene domains show almost exclusively either 0° or 30° interlayer rotations. Raman spectroscopy, transmission electron microscopy, and Fourier-transformed infrared spectroscopy were used to demonstrate that bilayer graphene domains with 0° interlayer stacking angles were Bernal stacked. Based on first-principle calculations, it is proposed that rotations originate from the graphene nucleation at the Cu step, which explains the origin of the interlayer rotations and agrees well with the experimental observations.
由于其丰富的电子和光学性质,双层和三层石墨烯引起了人们的浓厚兴趣,这些性质取决于层间旋转。然而,高质量大尺寸双层和三层石墨烯单晶的合成仍然是一个挑战。在这里,我们使用化学气相沉积法在 Cu 箔上合成了 100 μm 金字塔状六方双层和三层石墨烯单晶畴。所制备的石墨烯畴几乎只显示 0°或 30°的层间旋转。拉曼光谱、透射电子显微镜和傅里叶变换红外光谱用于证明具有 0°层间堆积角的双层石墨烯畴是伯纳尔堆叠的。基于第一性原理计算,提出了石墨烯在 Cu 台阶处的成核导致了层间的旋转,这解释了层间旋转的起源,并与实验观察结果吻合良好。