Applied Science and Convergence Technology

Charge Carrier Density Tuning of Graphene by Water Gating

Young-Jun Yu

Additional article information

Abstract

In this work, the conditions of water-gated carrier density accumulation on graphene were investigated. In particular, either negative or positive electric potential in deionized water could be observed, leading to an increase or decrease in the hole charge carrier density, respectively. Furthermore, it was determined that the critical positive electric potential for water gating of graphene is required to return the accumulated carrier density back to its initial state. Taken together, these results provide valuable insight into the relationship between carrier accumulation and the deionized water gating method.

Keywords: Graphene, Carrier density, Water gating

I. Introduction

Graphene has been favored for atomically thin electrodes for nano-scale devices due to its high electrical conductivity [13]. Since the high charge carrier doping condition of graphene is one of the critical requirements for high conductivity electrodes, the accumulation of carrier density on graphene has been extensively studied. The use of electrolytes to potentially produce highly doped graphene by various methods has also been investigated for applications in several fields [413]. However, when a critical electric potential is applied to graphene via electrolytes such as ionic liquid or gel [79], undesired sp3 bonds were observed to form on the graphene [413] Thus, in order to maintain distinct sp2 electric potential structures on graphene during the application of an electric gate voltage, a stable electrolyte is required. Water is a promising electrolyte for this use, and water-gated field effect transistors have previously been reported [5,12]. However, more detailed information regarding the carrier density variation of graphene with water-gating is required.

In this work, the behavior of carrier density accumulation on graphene is investigated. In particular, the ability to tune the carrier density when employing deionized (DI) water gating with electric potential is explored. Finally, detailed information regarding the effect of accumulating charge carriers on graphene when either negative or positive electric potential is supplied through DI-water is presented.

II. Experimental details

In order to identify graphene conductance, graphene was prepared on a 280-nm-thick silicon dioxide (SiO2)/highly doped silicon (Si) substrate by the mechanical exfoliation method. Subsequently, titanium (Ti) electrodes were placed in contact with graphene by a conventional electron-beam lithography process [Figs. 1(a) and 1(b)] [8,9,13]. Owing to the natural formation of a thin oxide layer on Ti when exposed to air, this oxide was employed as a barrier for blocking the interaction between the water-gate and Ti electrodes. As shown in Fig. 1(a), the resistance variation of graphene was inspected by two-terminal measurement during the application of either back-gate voltage (VBG) or water-gated voltage (VWG) through a SiO2/Si substrate or DI-water (resistivity = 8 ~ 10 MΩ)/platinum (Pt) bar, respectively.

Figure F1
(Color online) (a) Schematic diagram of water gating by a platinum bar for graphene FET with Ti electrodes. (b) Topography image of graphene FET in contact with Ti electrodes on ...

Figures 2(a) and 2(b) show the resistance of graphene as a function of VBG and VWG, respectively. As shown in these figures, the initially accumulated carrier density in graphene was n = (CBG/e) · VCNP-BG ≈ 5 × 1011 cm−2, where CBG = 12 nF/cm2 is the capacitance of the 280-nm-thick SiO2 substrate, e is the charge of an electron, and VCNP-BG = 8.35 V is the charge neutral point. When DI-water gating is used instead of the SiO2 substrate for the same graphene, the charge neutral point VCNP-WG = 0.15 V. The capacitance of DI-water (CWG) was calculated to be CWG = 668 nF/cm2, because the initial accumulation of carrier density under applied VBG corresponded with the accumulated density under applied VWG as follows,

Figure F2
Resistance variation of graphene as a function of (a) back-gate voltage, VBG and (b) water-gate voltage, VWG.

n = ( C BG / e ) · V CNP-BG = ( C WG / e ) · V CNP-WG
(1)
[1012,14]

III. Results and discussion

Figure 3 shows the resistance of graphene as a function of time for different values of applied VWG. When the (1) VWG = −0.6 V was applied to graphene, a decreased resistance of approximately 4.4 kΩ was observed. Subsequently, the resistance of graphene was measured as 5.4 kΩ for (2) VWG = 0.6 V and as 4.3 kΩ for (7) VWG = 2.0 V. Furthermore, VWG = (1) −0.6 V, (6) 1.5 V, and (7) 2.0 V were gradually applied to graphene again as shown in the second light-green area within Fig. 3. Similar resistances of graphene were obtained from the first measurement denoted by the blue area in Fig. 3. Although, the variation of resistance as a function of VWG was observed, this result was not enough to clearly understand the effect of VWG on the accumulated carrier density variation on graphene. Thus, VCNP-BG from the resistance curves was represented as a function of VBG [Fig. 4] after each VWG at (1) ~ (7) were applied to graphene, as shown in Fig. 3.

Figure F3
(Color online) Resistance variation of graphene as a function of time for different applied VWG = (1) −0.6 V, (2) 0.7 V, (3) 0.9 V, (4) 1.0 V, (5) 1.2 ...
Figure F4
(Color online) (a) Resistance curves of graphene as a function of VBG after applied VWG from (1) −0.6 V to (7) 2.0 V. (b) Accumulated carrier density of graphene as ...

Figure 4(a) presents the resistance curves of graphene as a function of VBG after the application of VWG = (0) 0 V, (1) −0.6 V, and (3) 0.7 V ~ (7) 2.0 V. Compared with the neutral point of VCNP-BG = 8.35 V [marked by the black dashed line of the black transport curve in Fig. 4(a)] under (0) VWG = 0 V, VCNP-BG was increased by approximately 10 V [the red transport curve in Fig. 4(a)] for (1) −0.6 V and VCNP-BG remained approximately 10 V during the application of VWG = (2) 0.7 ~ (5) 1.2 V [denoted by the dashed transport curves in Fig. 4(a)]. When VWG greater than (6) 1.5 V and (7) 2.0 V was applied [the blue and brown transport curves in Fig. 4(a)], VCNP-BG decreased by approximately 3 V.

As an estimate of the variation of the accumulated carrier density (n), Fig. 4(b) exhibits the relationship between n and VWG. The accumulated carrier density was observed to be n = 5.09 × 1011 and 10.65 × 1011 cm−2 for VWG = (0) 0 V and (1) −0.6 V, respectively. As previously mentioned with regard to VCNP-WG in Fig. 4(a), although VWG = (2) 0.7 V ~ (5) 1.2 V were applied, the carrier density was maintained between n = 10 × 1011 and n = 13 × 1011 cm−2, as marked by pink area in Fig. 4(b). Meanwhile, n ≈ 2 × 1011 cm−2 was measured for VWG = (6) 1.5 V ~ (7) 2.0 V as marked by blue area in Fig. 4(b). Moreover, similar behavior [red dots in Fig. 4(b)] was also observed in the second cycle with the application of VWG = (1) −0.6 V, (6) 1.5 V, and (7) 2.0 V after finishing the first cycle in its entirety. This indicates that although water-gating leads to changes in the doping of graphene when negative electric potential (VWG = −0.6 V) is applied, a critical positive electric potential (VWG ≥ 1.5 V) can be applied to return accumulated carrier density to its initial condition from the highly p-doped condition generated by negative electric potential.

IV. Conclusions

In this work, carrier density accumulation was observed in response to DI-water gating. When a critical negative electric potential (VWG = −0.6 V) was applied via DI-water, the accumulated hole carrier density was observed. Furthermore, once the applied voltage exceeded a critical positive electric potential (VWG ≥ 1.5 V) through DI-water, this accumulated carrier density could be restored to the initial carrier density condition. This result provides meaningful insight into the relationship between carrier accumulation and the DI-water gating method.

Acknowledgements

This work was supported by the research fund of Chungnam National University.

Article information

Applied Science and Convergence Technology.Nov 30, 2019; 28(6): 226-228.
Published online 2019-11-30. doi:  10.5757/ASCT.2019.28.6.226
Department of Physics, Chungnam National University, Daejeon 34134, Republic of Korea
Received November 18, 2019; Accepted December 5, 2019.
Articles from Applied Science and Convergence Technology are provided here courtesy of Applied Science and Convergence Technology

References

  • Yu YJ, Zhao Y, Ryu S, Brus LE, Kim KS, and Kim P. Nano Lett 2009;9:3430.

Figure 1


(Color online) (a) Schematic diagram of water gating by a platinum bar for graphene FET with Ti electrodes. (b) Topography image of graphene FET in contact with Ti electrodes on an SiO2/Si substrate. Here it was utilized highly doped silicon substrate for applying back-gate voltage, VBG.

Figure 2


Resistance variation of graphene as a function of (a) back-gate voltage, VBG and (b) water-gate voltage, VWG.

Figure 3


(Color online) Resistance variation of graphene as a function of time for different applied VWG = (1) −0.6 V, (2) 0.7 V, (3) 0.9 V, (4) 1.0 V, (5) 1.2 V, (6) 1.5 V and (7) 2.0 V. The water-gating ranges from VWG = (1) −0.6 V to (7) 2.0 V were applied twice, with the first and second applications denoted by the blue and green areas, respectively.

Figure 4


(Color online) (a) Resistance curves of graphene as a function of VBG after applied VWG from (1) −0.6 V to (7) 2.0 V. (b) Accumulated carrier density of graphene as a function of VWG for (0) 0.0 V, (1) −0.6 V, (2) 0.7 V ~ (5) 1.2 V, and (6) 1.5 V ~ (7) 2.0 V. Black and red dots indicate the n for the first and second cycles of VWG application.