We have found that the Berry phase of bilayer graphene becomes p from 2p estimated by Shubnikov-de Haas oscillations when the A-B stacked pristine bilayer graphene experiences the Li-intercalation and sequential Li-desorption process in ultrahigh vacuum. Furthermore, the mobility of such processed bilayer graphene increases around four times larger, ~ 8,000 cm 2 /V·s, than that of the pristine bilayer graphene. This is mainly due to increment of the scattering time and decrement of the cyclotron mass, * akiyama@surface.phys.s.u-tokyo.ac.jp 2 which can be interpreted as a result of the change of the stacking structure of bilayer graphene from A-B to A-A, corresponding to a change from the parabolic to the linear band dispersion.
3Monolayer graphene is well known to be a two-dimensional (2D) [5][6][7]. This difference between the A-B and A-A stacked BLGs, of course, causes some difference in their physical and electronic properties. Especially, the Berry phase is different between the two systems; that of Dirac system is π, while that of Schrödinger system is 2π.In spite of these remarkable characteristics of BLG, the method of fabricating the A-A stacked BLG has not been reported yet except for the local observation [8,9]. This is because the A-B stacking is energetically more favorable than the A-A stacking [10]. In a recent study, however, Li-intercalated BLG was found to take the A-A stacked form with Li atoms intercalated at the center of the hexagons in the upper and lower graphene sheets [11]. Bulky graphite Li-intercalation compound (GIC) is also known to 4 be in the A-A stacking [12,13].In this study, it is suggested, based on ex situ measurements of Shubnikov - The samples used in the present study were pristine BLG (Sample A),Li-intercalated BLG [14], and Li-desorbed BLG (Sample B). Their RHEED patterns are shown in Fig. 1 (a) -(c), respectively. Sample A was prepared on a n-type Si-rich 6H-SiC (0001) substrate by heating up to 1550°C in UHV (3 × 10 -10 Torr). Because the heating temperature and the keeping time were optimized, we have successfully fabricated exclusively BLG. As seen in Fig. 1(a), Sample A showed both the graphene 1×1 pattern (indicated by red arrows) and the buffer layer 6√3×6√3 R30° pattern (indicated by blue arrows). For preparing Sample B, Li was first deposited on the BLG using a Li dispenser (SAES Getters) at room temperature in UHV. This Li-intercalated BLG sample showed a RHEED pattern of √3×√3 R30° (indicated by yellow arrows) as shown in Fig. 1(b) [14,10,15]. Such a RHEED pattern reflects Li atoms arranged regularly in the interlayer space. Here, the green arrows show the SiC substrate 1×1 5 pattern. Then, it was heated up at 900°C to desorb Li atoms until the √3×√3 R30° pattern disappeared and the 6√3×6√3 R30° pattern from the buffer layer revived as shown in Fig. 1(c). This is Sample B.The samples were taken out from the UHV chamber, and bonded to Au wires with Indium to form the conventional 6-terminal methods. All electrical transport measurements were performed w...