Skip to main content
Sensors (Basel, Switzerland) logoLink to Sensors (Basel, Switzerland)
letter
. 2017 Jun 22;17(7):1476. doi: 10.3390/s17071476

The Resistance–Amplitude–Frequency Effect of In–Liquid Quartz Crystal Microbalance

Xianhe Huang 1,*, Qingsong Bai 1, Qi Zhou 1, Jianguo Hu 1
PMCID: PMC5539828  PMID: 28640210

Abstract

Due to the influence of liquid load, the equivalent resistance of in-liquid quartz crystal microbalance (QCM) increases sharply, and the quality factor and resonant frequency decreases. We found that the change in the resonant frequency of in-liquid QCM consisted of two parts: besides the frequency changes due to the mass and viscous load (which could be equivalent to motional inductance), the second part of frequency change was caused by the increase of motional resistance. The theoretical calculation and simulation proved that the increases of QCM motional resistance may indeed cause the decreases of resonant frequency, and revealed that the existence of static capacitance was the root cause of this frequency change. The second part of frequency change (due to the increases of motional resistance) was difficult to measure accurately, and may cause great error for in-liquid QCM applications. A technical method to reduce the interference caused by this effect is presented. The study contributes to the accurate determination of the frequency and amplitude change of in-liquid QCM caused by liquid load, which is significant for the QCM applications in the liquid phase.

Keywords: quartz crystal microbalance (QCM), equivalent circuit, resistance-amplitude-frequency effect, in-liquid QCM

1. Introduction

Quartz crystal microbalance (QCM) has been used for a long time in vacuum and gaseous environments as an ultrasensitive mass sensor, especially for film thickness monitoring [1,2], humidity sensors [3,4,5], proximity sensors [6,7], and various gas sensors [8,9,10]. A QCM device typically consists of a thin disk of AT-cut quartz crystal with circular electrodes patterned on both sides. Due to the piezoelectric properties and crystalline orientation of quartz, the alternating voltage between the electrodes excites crystal oscillating in a thickness shear mode. With varying mass attached to one side of the electrode, the QCM resonant frequency changes accordingly. The fundamental theory describing the relationship between frequency change and mass change was derived by Sauerbrey [11]; however, this theory is limited to the assumption that the mass deposition forms a thin, rigid film and that the mass sensitivity is uniform over the entire surface [12]. Since Nomura and Okuhara [13] showed that a QCM completely immersed in a liquid could also be excited to stable oscillation [14]—which marked the beginning of the QCM’s applications in liquid phase—QCM has often been applied as electrochemistry sensors [15,16,17], biosensors [18,19,20,21], and immunosensors [22,23,24,25].

It is convenient to use a lumped-parameter equivalent circuit to characterize a QCM for a narrow range of frequencies near resonance. In such a frequency range, the circuit parameters can be considered constant. Several years before the discovery of the piezoelectric resonator, Van Dyke and Butterworth showed that any mechanically vibrating system driven by means of an electrostatic field could be represented by the Butterworth-Van Dyke (BVD) equivalent circuit [26,27]. Therefore, the BVD equivalent circuit is typically used to describe the unloaded QCM (Figure 1a). In the BVD model, C0, C1, L1, and R1 are the static capacitance, motional capacitance, motional inductance, and motional resistance for unloaded QCM, respectively.

Figure 1.

Figure 1

The Butterworth-Van Dyke (BVD) equivalent circuit for (a) an unloaded quartz crystal microbalance (QCM); and (b) a QCM under viscous and mass loading.

However, in-liquid QCM applications are more important and complex, as the existence of a liquid load causes sharp increases of equivalent resistance and resonance damping, which consequently decreases the quality factor and resonant frequency. Martin et al. presented a model of an equivalent circuit for in-liquid QCM, which is shown in Figure 1b [28]. In Martin’s model, the influence caused by a liquid load was divided into mass loading and viscous loading; inductance L2 and resistance R2 were used to approximate the impedance of the viscous loading; inductance L3 was used to approximate the impedance of the mass loading; and capacitance Cp was used to express the parasitic capacitance of the test fixture [28]. In general, the increased resistance R2 (caused by viscous loading) was much larger than R1, which is the motional resistance of unloaded QCM. The increased inductance (L2 and L3) and the increased resistance (R2) caused by viscous loading resulted in the decreases of QCM resonant frequency.

It is noteworthy that the resonant frequency f we measured in most in-liquid QCMs was the S21 minimum impedance frequency rather than the zero-phase frequency, where S21 is an S-parameter which represents the forward transmission coefficient of two-port networks. There were two reasons: (1) for practical in-liquid QCM applications, when equivalent resistance increased to a certain degree, the S21 phase curve could not reach zero (that is, the zero-phase frequency would disappear); and (2) due to the existence of scatter phase shift in circuits, the actual oscillation frequency of oscillators was the minimum impedance frequency instead of the zero-phase frequency.

2. Theory and Simulation

The equivalent circuit of QCM loaded with liquid could be divided into the static arm branch and the motional arm branch. The static arm branch contained C0 and Cp, where Cp is the parasitic capacitance arising in the test fixture; and C0 is the static capacitance arising from the two electrodes separated by the insulating quartz and is a function of the electrodes size, shape, and configuration. Due to the piezoelectric effect of quartz crystal, the electromechanical coupling gave rise to the motional arm branch (C1, L1, R1, L2, R2, and L3). If we define that, the impedance of the static arm branch (Zs) and the motional arm branch (Zm) can be obtained:

Zs=1/jωC* (1)
Zm=R*+jωL*+1/jωC1 (2)

where C*=C0+Cp; R*=R1+R2; L*=L1+L2+L3; and ω=2πf. Consequently, the total impedance Z and admittance Y of the in-liquid QCM are obtained:

Z=ZsZmZs+Zm=1ω2L*C1+jωR*C1ω2R*C*C1jω3L*C*C1+jω(C*+C1) (3)
Y=R*R*2+(ωL*1/ωC1)2+j[(ωL*1/ωC1)R*2+(ωL*1/ωC1)2+ωC*] (4)

Therefore, the resonant frequency f is the frequency at the point of minimum impedance Zmin (or the point of maximum admittance Ymax).

The increased inductance L2+L3 caused by mass and viscous loading is what we normally think of as the reason for change in QCM resonant frequency: since the resonant frequency f=1/(2πL*C1), where L*=L1+L2+L3 and L1L2+L3, and C1 would not change for mass or viscous loading, therefore the fractional change of resonant frequency is as in Reference [28].

ΔfLf=ΔL2L*=(L2+L3)2(L1+L2+L3) (5)

Nevertheless, it is worth noting that increased motional resistance may also lead to resonant frequency change. Unfortunately, only the resonance damping caused by the added motional resistance has been considered, but the resonant frequency change caused by the added motional resistance had long remained unknown.

The calculated results of the equivalent circuit illustrated the resonant frequency change caused by the added motional resistance. The equivalent electronic parameters of an AT-cut 10 MHz QCM with one surface loaded by a drop of lube oil were measured. Considering that liquid loading results in great increases of resonance damping and great decreases of Q factor, the short-term frequency stability worsens significantly; therefore, we adopted a passive forward transmission measurement method with a vector network analyzer (Agilent E5062A). The radius of the oil drop was approximately 1.2 mm. The diameters of the crystal wafer and gold electrode were 8.7 and 5.1 mm, and the thicknesses of the gold electrodes and quartz crystal wafer were about 1000 Å and 0.167 mm, respectively. Due to the droplet loading, the measured resonance frequency decreased from 9.999873 MHz to 9.992959 MHz. The static capacitance C0 of the QCM was 6.0 pF; and the parasitic capacitance Cp formed in the test fixture was about 2.5 pF. The motional capacitance C1 of the QCM was 27.0 fF. The motional resistance R1 of the unload QCM and the motional resistance R2 caused by oil loading were approximately 12 Ω and 690 Ω, respectively. The motional inductance L*=L1+L2+L3 of the loaded QCM was about 9.3816 mH, where L1L2+L3.

Table 1 shows the calculation results obtained by MATLAB software (The Math Works, Inc.) using the BVD equivalent circuit model. The resonant frequency and resonant amplitude of QCM with and without added motional resistance were calculated. It was clear that when other parameters remained constant, the motional resistance increase caused both frequency change and resonance damping simultaneously. The resonant frequency change ΔfR caused by the added motional resistance was influenced by the static capacitance C*: ΔfR increased sharply along with C* increasing. Moreover, the resonance damping caused by the added motional resistance decreased along with C* increasing. That is, the smaller the static capacitance C*, the larger the resonance damping caused by the added motional resistance.

Table 1.

The calculated results using the BVD equivalent circuit model.

R* (Ω) L* (mH) C1 (fF) C* (pF) f (Hz) ΔfR(Hz) Resonance Damping (dB)
Group 1 12 9.3816 27 0.0 9,999,995 0 –0.984
702 9.3816 27 0.0 9,999,995 –18.083
Group 2 12 9.3816 27 1.0 9,999,995 262 –0.984
702 9.3816 27 1.0 9,999,733 –18.065
Group 3 12 9.3816 27 3.5 9,999,995 898 –0.984
702 9.3816 27 3.5 9,999,097 –17.860
Group 4 12 9.3816 27 6.0 9,999,995 1478 –0.984
702 9.3816 27 6.0 9,998,517 –17.470
Group 5 12 9.3816 27 8.5 9,999,995 1983 –0.984
702 9.3816 27 8.5 9,998,012 –16.959

To illustrate the resistance-amplitude-frequency effect of in-liquid QCM more clearly, simulations were carried out using business software Advanced Design System (Agilent Technologies, Inc. Santa Clara, CA, USA) a professional commercial circuit simulation tool software and well suited to simulate the circuit’s S-parameters. The scheme of the BVD equivalent circuit simulation is shown in Figure 2. Using Groups 3–5 in Table 1 as instances, the S21 parameters vs. frequency curve with and without the added motional resistance are shown as Figure 3, Figure 4 and Figure 5, which reflect the same phenomenon.

Figure 2.

Figure 2

The Butterworth-Van Dyke (BVD) equivalent circuit schematic of Advanced Design System (ADS) simulation.

Figure 3.

Figure 3

When C* = 3.5 pF, the S21 parameters vs. frequency curve with and without added motional resistance.

Figure 4.

Figure 4

When C* = 6.0 pF, the S21 parameters vs. frequency curve with and without added motional resistance.

Figure 5.

Figure 5

When C* = 8.5 pF, the S21 parameters vs. frequency curve with and without added motional resistance.

By comparing the data in Table 1 and Figure 3, Figure 4 and Figure 5, the resonance damping caused by the added motional resistance was the same, and the changes in resonance frequency were different, but had the same trend. The reason leading to different resonance frequency shifts between the calculation results and the simulations was that two 50 Ohm impedances were added at each port when using the Advanced Design System (ADS) software to simulate the equivalent circuit. On the other hand, the symmetry of the two added impedances at two ports in the ADS simulations could eliminate the influence of the added impedances on the resonance damping simulations. Therefore, the resonance damping in the calculation and simulation results had the same values, and the resonance frequency changes in calculation and simulation results had different values but reflected the same trend.

3. Discussion

For in-liquid QCM applications, the viscous coupling of the contact liquid to the quartz crystal resonator surface resulted in decreases in both the resonant frequency of the QCM and damping of the resonance. Traditional knowledge has suggested that the resonance damping is only caused by the added equivalent resistance R2, and the resonant frequency change was only caused by the added equivalent inductance L2+L3. However, both the theoretical calculations and simulations proved that the added equivalent resistance R2 also caused resonant frequency change. Therefore, the in-liquid QCM resonant frequency change is comprised of two parts: the frequency change ΔfL caused by the added equivalent motional inductance L2+L3; and the frequency change ΔfR caused by the added resonant motional resistance R2. In actual measurements, the measured frequency change was Δf=ΔfL+ΔfR, but the theoretical frequency change as per Equation (5) was just ΔfL and did not contain ΔfR. Although ΔfR was smaller than ΔfL in most applications, the influence of ΔfR could not be ignored, especially in in-liquid QCM with large motional capacitance, as ΔfR increased sharply along with increasing C*.

Currently, the frequency change ΔfR is not easily measured accurately, which is an important area of future research. As we could not change the equivalent resistance alone in the actual experiment (the addition of a resistor in series with QCM could not model the increase of equivalent resistance), it was hard to isolate the frequency change ΔfR caused by the added resonant motional resistance R2. Therefore, the existence of unpredictable ΔfR will lead to errors for in-liquid QCM applications. To resolve these issues, a possible solution was presented: to add an inductance La (make the resonant frequency of the oscillating circuit that consists of La and C* equal to f) to eliminate the influence of R2 on resonant frequency, as Figure 6 shows.

Figure 6.

Figure 6

The equivalent circuit for an in-liquid QCM after the addition of inductance La.

Using Group 5 in Table 1 as an example, the S21 parameters vs. frequency curve after added the inductance La is shown in Figure 7. By comparing Figure 5 and Figure 7, it was clear that the addition of La with a value of 29.8 µH, the resonance frequency change caused by the added resistance decreased from 2534 Hz to 9 Hz. Furthermore, resonance damping also increased.

Figure 7.

Figure 7

When C* = 8.5 pF, the S21 parameters vs. frequency curve after the addition of inductance La.

4. Conclusions

For in-liquid QCM applications, the liquid load was equivalent to a mass loading (L3) and a viscous loading (L2+R2). The viscous coupling of the contact liquid to the QCM surface led to decreases in resonant frequency and increases in resonance damping. Unlike previous notions, motional resistance caused by viscous loading resulted not only in resonance damping, but also resonance frequency change. Furthermore, the resonant frequency change caused by the added motional resistance increased sharply along with increases in static capacitance. In addition, the resonance damping caused by the added motional resistance decreased along with static capacitance increasing. These results will be instrumental in understanding in-liquid QCM characterization, which is of importance in in-liquid QCM applications.

Author Contributions

X.H.H. conceived and designed the experiments, and performed the simulations and calculations; Q.S.B. helped perform the simulations and calculations, and was in charge of the paper writing; Q.Z. took part in the revision process; J.G.H. took part in the discussion of the results; and X.H.H. as group leader was responsible for project management and the revision of this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  • 1.Fukao N., Kyung K.H., Fujimoto K., Shiratori S. Automatic Spray-LBL Machine Based on in-Situ QCM Monitoring. Macromolecules. 2011;44:2964–2969. doi: 10.1021/ma200024w. [DOI] [Google Scholar]
  • 2.Huang H.L., Xu Y., Hong Y.L. Effects of film thickness on moisture sorption, glass transition temperature and morphology of poly(chloro-p-xylylene) film. Polymer. 2005;46:5949–5955. doi: 10.1016/j.polymer.2005.05.076. [DOI] [Google Scholar]
  • 3.Yao Y., Ma W.Y. Self-Assembly of Polyelectrolytic/Graphene Oxide Multilayer Thin Films on Quartz Crystal Microbalance for Humidity Detection. IEEE Sens. J. 2014;14:4078–4084. doi: 10.1109/JSEN.2014.2332881. [DOI] [Google Scholar]
  • 4.Pascal-Delannoy F., Sorli B., Boyer A. Quartz Crystal Microbalance (QCM) used as humidity sensor. Sens. Actuators A Phys. 2000;84:285–291. doi: 10.1016/S0924-4247(00)00391-5. [DOI] [Google Scholar]
  • 5.Yao Y., Chen X.D., Li X.Y., Chen X.P., Li N. Investigation of the stability of QCM humidity sensor using graphene oxide as sensing films. Sens. Actuators B Chem. 2014;191:779–783. doi: 10.1016/j.snb.2013.10.076. [DOI] [Google Scholar]
  • 6.Yao Y., Zhang H., Huang X.H. Enhanced sensitivity of quartz crystal proximity sensors using an asymmetrical electrodes configuration. Sens. Actuators A Phys. 2017;258:95–100. doi: 10.1016/j.sna.2017.03.001. [DOI] [Google Scholar]
  • 7.Chang W.T. Metal-electrode-sandwiched quartz crystal-based oscillator as proximity sensor. Sens. Actuators A Phys. 2011;171:292–296. doi: 10.1016/j.sna.2011.07.010. [DOI] [Google Scholar]
  • 8.Procek M., Stolarczyk A., Pustelny T., Maciak E. A Study of a QCM Sensor Based on TiO2 Nanostructures for the Detection of NO2 and Explosives Vapours in Air. Sensors. 2015;15:9563–9581. doi: 10.3390/s150409563. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Wang X.F., Ding B., Sun M., Yu J.Y., Sun G. Nanofibrous polyethyleneimine membranes as sensitive coatings for quartz crystal microbalance-based formaldehyde sensors. Sens. Actuators B Chem. 2009;144:11–17. doi: 10.1016/j.snb.2009.08.023. [DOI] [Google Scholar]
  • 10.Selyanchyn R., Korposh S., Wakamatsu S., Lee S.W. Respiratory Monitoring by Porphyrin Modified Quartz Crystal Microbalance Sensors. Sensors. 2011;11:1177–1191. doi: 10.3390/s110101177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Sauerbrey G. Use of quartz vibration for weighing thin films on a microbalance. Z. Phys. 1959;155:206–212. doi: 10.1007/BF01337937. [DOI] [Google Scholar]
  • 12.Hillier A.C., Ward M.D. Scanning electrochemical mass sensitivity mapping of the quartz crystal microbalance in liquid media. Anal. Chem. 1992;64:2539–2554. doi: 10.1021/ac00045a014. [DOI] [Google Scholar]
  • 13.Nomura T., Okuhara M. Frequency shift of piezoelectric quartz crystals immersed in organic liquids. Anal. Chim. Acta. 1982;142:281–284. doi: 10.1016/S0003-2670(01)95290-0. [DOI] [Google Scholar]
  • 14.Sato T., Izyan Ruslan R., Goto S., Akitsu T. Double-Resonance Quartz Crystal Oscillator and Excitation of a Resonator Immersed in Liquid Media. IEEE Trans. Ultrason. Ferroelectr. Freq. Control. 2011;58:788–797. doi: 10.1109/TUFFC.2011.1871. [DOI] [PubMed] [Google Scholar]
  • 15.Sigalov S., Levi M.D., Salitra G., Aurbach D., Maier J. EQCM as a unique tool for determination of ionic fluxes in microporous carbons as a function of surface charge distribution. Electrochem. Commun. 2010;12:1718–1721. doi: 10.1016/j.elecom.2010.10.005. [DOI] [Google Scholar]
  • 16.Levi M.D., Sigalov S., Salitra G., Aurbach D. Quartz crystal microbalance with dissipation monitoring (EQCM-D) for in-situ studies of electrodes for supercapacitors and batteries: A mini-review. Electrochem. Commun. 2016;67:16–21. doi: 10.1016/j.elecom.2016.03.006. [DOI] [Google Scholar]
  • 17.Tsai W.-Y., Taberna P.L., Patrice S. Electrochemical quartz crystal microbalance (EQCM) study of ion dynamics in nanoporous carbons. J. Am. Chem. Soc. 2014;136:8722–8728. doi: 10.1021/ja503449w. [DOI] [PubMed] [Google Scholar]
  • 18.Diltemiz S.E., Keçili R., Ersöz A., Say R. Molecular Imprinting Technology in Quartz Crystal Microbalance (QCM) Sensors. Sensors. 2017;17:454. doi: 10.3390/s17030454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Yao C.Y., Qu L., Fu W.L. Detection of Fibrinogen and Coagulation Factor VIII in Plasma by a Quartz Crystal Microbalance Biosensor. Sensors. 2013;13:6946–6956. doi: 10.3390/s130606946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Cho N.J., Frank C.W., Kasemo B., Hook F. Quartz crystal microbalance with dissipation monitoring of supported lipid bilayers on various substrates. Nat. Protoc. 2010;5:1096–1106. doi: 10.1038/nprot.2010.65. [DOI] [PubMed] [Google Scholar]
  • 21.Yao C.Y., Zhu T.Y., Qi Y.Z., Zhao Y.H., Xia H., Fu W.L. Development of a Quartz Crystal Microbalance Biosensor with Aptamers as Bio-recognition Element. Sensors. 2010;10:5859–5871. doi: 10.3390/s100605859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Xiao Y.H., Liu Y., Borg G., Withers R.L., Li Z.R., Xu Z., Li C.M. Lead magnesium niobate-lead titanate piezoelectric immunosensors. Sens. Actuators A Phys. 2010;163:82–87. doi: 10.1016/j.sna.2010.07.011. [DOI] [Google Scholar]
  • 23.Yang Y., Tu Y.F., Wang X.S., Pan J.Y., Ding Y. A Label-Free Immunosensor for Ultrasensitive Detection of Ketamine Based on Quartz Crystal Microbalance. Sensors. 2015;15:8540–8549. doi: 10.3390/s150408540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Akter R., Rhee C.K., Rahman M.A. A highly sensitive quartz crystal microbalance immunosensor based on magnetic bead-supported bienzymes catalyzed mass enhancement strategy. Biosens. Bioelectron. 2015;66:539–546. doi: 10.1016/j.bios.2014.12.007. [DOI] [PubMed] [Google Scholar]
  • 25.Ertekin Ö., Öztürk S., Öztürk Z.Z. Label Free QCM Immunobiosensor for AFB1 Detection Using Monoclonal IgA Antibody as Recognition Element. Sensors. 2016;16:1274. doi: 10.3390/s16081274. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Butterworth S. On Electrically-maintained Vibrations. Proc. Phys. Soc. Lond. 1914;27:410–424. doi: 10.1088/1478-7814/27/1/330. [DOI] [Google Scholar]
  • 27.Van Dyke K.S. The piezo-electric resonator and its equivalent network. Proc. Inst. Radio Eng. 1928;16:742–764. doi: 10.1109/JRPROC.1928.221466. [DOI] [Google Scholar]
  • 28.Martin S.J., Granstaff V.E., Frye G.C. Characterization of a quartz crystal microbalance with simultaneous mass and liquid loading. Anal. Chem. 1991;63:2272–2281. doi: 10.1021/ac00020a015. [DOI] [Google Scholar]

Articles from Sensors (Basel, Switzerland) are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES