, Volume 25, Issue 1, pp 7–15 | Cite as

Novel piezoelectric paper based on SbSI nanowires

  • Bartłomiej Toroń
  • Piotr SzperlichEmail author
  • Marian Nowak
  • Danuta Stróż
  • Tomasz Rzychoń
Open Access


A novel piezoelectric paper based on antimony sulfoiodide (SbSI) nanowires is reported. The composite of tough sonochemically produced SbSI nanowires (with lateral dimensions 10–100 nm and length up to several micrometers) with very flexible cellulose leads to applicable, elastic material suitable to use in fabrication of, for example, piezoelectric nanogenerators. For mechanical energy harvesting, cellulose/SbSI nanocomposite may be used. Due to its high values of electromechanical coefficient (k33 = 0.9) and piezoelectric coefficient (d33 = 1 × 10−9 C/N), SbSI is a very attractive material for such devices. The preliminary investigations of a simple cellulose/SbSI nanogenerator for shock pressure (p = 3 MPa) and sound excitation (f = 175 Hz, Lp = 90 dB) allowed to determine its open circuit voltage 2.5 V and 24 mV, respectively. For a load resistance equal to source impedance (ZS = 2.90(11) MΩ), maximum output power density (PL = 41.5 nW/cm3 for 0.05-mm-thick sheet of this composite) of the cellulose/SbSI nanogenerator was observed. Cellulose/SbSI piezoelectric paper may also be useful to construct gas nanosensors and actuators.


Piezoelectric paper Antimony sulfoiodide Nanowires Piezoelectric semiconductors 


Currently, a great demand for energy harvesting is observed. The first piezoelectric nanogenerator (NG) based on zinc oxide nanowires for mechanical to electrical energy conversion was proposed by Wang and Song (2006). It started with promising investigations on such devices, for example, to harvest vibrations (Chen et al. 2010, 2013; Poulin-Vittrant et al. 2015; Zhan et al. 2014), human body motion (Lee et al. 2014; Yang et al. 2009), wind (Gao et al. 2015), acoustic waves (Wang et al. 2007), and other mechanical energy forms (Wang 2012). Piezoelectric generators are also used as passive or self-powered sensors (Chen et al. 2013; Fan et al. 2012; Fang et al. 2015; Hua and Wang 2015). Fabrication of a mechanically flexible, piezoelectric nanocomposite material consisting of zinc oxide (ZnO) nanostructures embedded in a stable matrix of cellulose fibers was presented by Gullapalli et al. (2010). They reported applicability of this piezoelectric paper as a strain sensor. Kumar et al. (2011) demonstrated that nanocomposite consisting of ZnO nanostructures embedded in a common paper matrix can be directly used as energy-conversion devices to transform mechanical energy to electric power (with output voltage and power up to 80 mV and 50 nW/cm2, respectively). Mahadeva et al. (2014) developed hybrid piezoelectric paper through fiber functionalization that involves anchoring nanostructured barium titanate (BaTiO3). This paper had the largest piezoelectric coefficient, d33 = 4.8(4) × 10−12 C/N, at the highest nanoparticle loading of 48 wt% BaTiO3. Paper-based piezoelectric generator made of bacterial cellulose and BaTiO3 was presented by Zhang et al. (2016).

Recently, antimony sulfoiodide (SbSI) nanowires have been applied for ferroelectric nanogenerator operating under shock pressure (Mistewicz et al. 2016). Also, electrospun polyacrylonitrite (PAN) fibers containing SbSI nanowires have been used to construct a simple PAN/SbSI piezoelectric generator (Nowak et al. 2017). The amplitude of the voltage pulse, generated under shock pressure of 3.0 MPa, has reached 180 V in this nanogenerator. The peak output voltage of about 0.2 V was measured in bending/releasing conditions with the deformation frequency of 1 Hz (Nowak et al. 2017).

Due to its high values of electromechanical coefficient k33 = 0.9 (Hamano et al. 1965) and piezoelectric coefficient d33 = 1 × 10−9 C/N (Grekov et al. 1973), it should be underlined that SbSI is very attractive for piezoelectric generators. Textured polycrystalline SbSI was used for the construction of actuators (Nowak et al. 2009b). The Curie temperature of ferroelectric SbSI nanowires [TC = 292(1) K (Szperlich et al. 2009)] is close to room temperature. But, the coexistence of ferroelectric and paraelectric phases is observed in SbSI crystals at rather wide range of temperatures, for example, 38 K (Zadorozhnaya et al. 1973). An increase in the Curie temperature to 338 K was reported for an ingot of the composition SbS0.8O0.2I (Nitsche et al. 1964).

In this paper, we present the fabrication of novel piezoelectric paper based on SbSI nanowires for the first time. Preliminary investigations of nanogenerators made of this material are also reported.


Figure 1 summarizes the fabrication of cellulose/SbSI composite. At first, SbSI nanowires were sonochemically synthesized from pure elements (antimony, sulfur, and iodine). In a typical procedure, the stoichiometric mixture of elements (e.g., 0.250 g S, 0.949 g Sb, and 0.990 g I2) was placed in 4 ml of ethanol in polypropylene container closed by polyethylene plug to avoid outflow of volatile synthesis products. The container was submerged in water in cup-horn of 750 W ultrasonic processor VCX-750 equipped with sealed converter VC-334 (Sonics & Materials, Inc.). Ultrasound frequency was 20 kHz, and the power density guaranteed by the manufacturer was 565 W/cm2. The water was kept at constant temperature (293 K) by refrigerated circulating bath AD07R (PolyScience). Using spectrophotometer PC-2000 (Ocean Optics Inc.) equipped with the ISP-REF integrating sphere (Ocean Optics Inc.), the process was monitored ex situ by diffuse reflectance spectroscopy (DRS).
Fig. 1

Scheme of sonochemical preparation of cellulose/SbSI nanocomposite: a initial elements (sulfur, antimony, and iodine) were sonicated in ampoule filled with ethanol; b SbSI nanowires were obtained after 2 h of sonication; c cellulose fibers and SbSI nanowires (10 times rinsed in ethanol) were sonicated together in water; d homogenous mixture of cellulose and SbSI nanowires were obtained after 2 h

The synthesis was continued to obtain red–orange gel with absorption edge of SbSI clearly identified (Fig. 2a). The whole synthesis process was performed for 2 h.
Fig. 2

a Diffuse reflectance of sonochemically produced SbSI sol (curve a), cellulose (curve b), and cellulose/SbSI composite (curve c); b the powder XRD pattern of SbSI nanowires; c EDS spectrum of sonochemically prepared SbSI nanowires

The gel was rinsed 10 times with pure ethanol to remove remaining substrate and centrifuged to extract the product using the MPW-223e centrifuge (MPW Med. Instruments). SbSI gel was dried under the pressure of 60 Pa at room temperature for 72 h. The xerogel consisted of SbSI nanowires. Their sizes and structures were determined using a JEOL-JEM 3010 microscope, working at a 300 kV accelerating voltage. Characterization of the SbSI gel was accomplished using other techniques, such as X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and selected area electron diffraction (SAED). The equipment and procedures were the same as presented by Nowak et al. (2008, 2014).

Cellulose fibers, from International Paper Co. (Kwidzyn), with lateral dimensions of 10–25 μm and length up to a few millimeters were sonically dispersed in water. In the next step, SbSI xerogel was added to them in the mass ratio 1:4. Ultrasound irradiation was used again for 2 h to ensure homogeneous mixture of cellulose fibers and SbSI nanowires. The dilute suspension of cellulose fibers/SbSI nanowires was deposited on blotting paper and pressed to make sheets of cellulose/SbSI nanocomposite (cellulose/SbSI NC). Typical thickness of these sheets was 0.05 mm. Phenom PRO X scanning electron microscope (Phenom World) equipped with EDS detector was used to study the morphology and chemical composition of the products.

The prepared cellulose/SbSI NC sheets (Fig. 3a) were used as active layers in fabricated nanogenerators. First, the 10 × 10 mm2 sample was cut from cellulose/SbSI NC (Fig. 3b). Thin-film gold electrodes (Fig. 3c) were deposited on both sides of it using sputter coater Q150T ES (Quorum). Cooper wires were connected to gold electrodes (Fig. 3d) using high-purity silver paste 05002-AB (SPI Supplies). Such prepared sample was coated with Elastosil N10 silicones rubber (DRAWIN Vertriebs-GmbH) to protect it from the influence of ambient moisture and mechanical failure (Fig. 3e). Figure 3f presents the photograph of fabricated cellulose/SbSI nanogenerator. Capacity 86 pF and tan Delta equal 0.05 were measured for f = 1 kHz using impedance analyzer 3532-50 LCR HITESTER (Hioki).
Fig. 3

Scheme of cellulose/SbSI nanogenerator assembly steps: a photo of cellulose/SbSI sheet; b sample cut from this sheet; c gold electrodes deposited on both sides of cellulose/SbSI sheet; d wires mounted by silver paste to the electrodes; e device coated with protective layer of silicones rubber; f photo of piezoelectric cellulose/SbSI nanogenerator

Functional parameters (generated voltage, current, and power) of cellulose/SbSI nanogenerators were measured at room temperature in ambient atmosphere. Acoustic waves were generated by a loudspeaker biased with function generator MXG-9802 (METEX). Samples were located on testing table while the loudspeaker was placed slightly over them to avoid influence of housing vibration on response characteristics. Using T-01 sound level meter (Sonopan), the sound pressure level was measured. To examine cellulose/SbSI NGs response on shock pressure, Zoraki HP-01 air gun (Atak Arms CO., LTD) was used. The air shock waves with approximately 144 m/s velocity and pressure of 3 MPa were pointed onto SbSI nanodevices. Shock pressure was measured with S-10 pressure sensor (WIKA Alexander Wiegand SE & Co. KG). Using DS 1202CA digital oscilloscope (Rigol) and EG&G 5110 dual phase lock in amplifier (Princeton Applied Research), open circuit voltages generated in cellulose/SbSI NGs were recorded. Measurements of U-I characteristics for different load resistances were performed using Zeal decade resistance box (1 Ω–1 GΩ). LabView program was developed for computer controlling the experiment, data acquisition and analysis.

Results and discussion

Figures 2b, c and 4a, respectively, present XRD, EDS, and SEM results. The powder XRD pattern shows well-defined peaks. It indicates that obtained product has high purity and is well crystallized. No peaks of any other phases are detected. All the diffraction peaks can be indexed to be a pure orthorhombic phase for SbSI with the cell constants such as a = 0.858 nm, b = 1.017 nm, and c = 0.414 nm. The identification was performed using the PCSIWIN computer program and the data from Antimony Sulfide Iodide (2000).
Fig. 4

a SEM micrograph of cellulose/SbSI nanocomposite; b magnification of SbSI nanowires filling free space among cellulose fibers; c HRTEM micrograph of SbSI nanowires showing clear Moir’ fringes; d fast Fourier transform (FFT) image of single SbSI nanowire marked in (c). The fringe spacings of d1 = 0.649(6) nm and d2 = 0.415(5) nm correspond to the interplanar distances of 0.64989 nm and 0.4160 nm between the (110) and (001) planes of SbSI crystal (Antimony Sulfide Iodide 2000), respectively

The product consisted of needle-shaped nanowires with lateral dimensions in the range from 10 to 50 nm, and the lengths up to several micrometers. The EDS spectrum (Fig. 2c) performed on these nanowires shows peaks for antimony, sulfur, and iodide only and confirms an elemental atomic ratio of 0.33:0.33:0.34 for sulfur, iodine, and antimony, respectively. It indicates a stoichiometric SbSI within the experimental error.

The HRTEM micrograph of a single SbSI nanowire (Fig. 4c, d) exhibited clear lattice fringes parallel to the nanowire axis. The fringe spacing of d1 = 0.649(6) nm and d2 = 0.415(5) nm corresponded to the interplanar distances of 0.64989 and 0.4160 nm between the (110) and (001) planes of orthorhombic structure of bulk SbSI (Antimony Sulfide Iodide 2000), respectively.

Absorption edge visible on DRS characteristic for cellulose/SbSI composite (Fig. 2a) is adequate to be observed for SbSI nanowires. Using the method presented in Nowak et al. (2009a), the energy gap of SbSI in the composite was determined. Value of this energy gap Eg = 1.835(23) eV is in good agreement with results presented previously for SbSI (Nowak et al. 2008). For wavelengths higher than 700 nm, the presence of cellulose fibers causes monotonous decrease of cellulose/SbSI reflectance coefficient.

Figures 4a, b show regularly dispersed SbSI nanowires among cellulose fibers connected all together. SbSI nanowires constitute 23% of composite mass. According to Nan and Jia (2015), the fabricated cellulose/SbSI NC can be qualified as so-called 0–3-type nanocomposite with SbSI nanowires randomly dispersed in a cellulose matrix. Composite of cellulose fibers and SbSI nanowires is much more elastic than bulk SbSI samples (measurements of the elasticity are in progress). Therefore, the cellulose/SbSI composite is much more suitable for fabrication of piezoelectric generators than SbSI crystals alone.

Figure 5a presents sinusoidal open circuit voltage of cellulose/SbSI nanogenerator for sound excitation. The signal peak is UOC(peak) = 42.0(12) mV, which gives RMS voltage UOC(RMS) = 29.7(9) mV for Lp = 90 dB sound pressure level. The ratio of cellulose/SbSI NG voltage response to sound pressure level increases with the frequency of acoustical signal (Fig. 5b), attains maximum for fREZ = 175 Hz, and then decreases. The fREZ is resonance frequency depending on the mass of the sample and its stiffness coefficient. The latter is influenced by the flexibility and relaxation delay of cellulose fibers responsible for elastic properties of NG. This is a common phenomenon for paper NGs (Nan and Jia 2015).
Fig. 5

a Open circuit response of cellulose/SbSI nanogenerator for sound excitation (f = 175 Hz, Lp = 90 dB). b Normalized frequency spectrum of UOC(RMS) response of cellulose/SbSI nanogenerator

Figure 6a shows output voltage UL(RMS) of cellulose/SbSI nanogenerator for sinusoidal sound wave excitation (f = 175 Hz, Lp = 90 dB) as a function of current density calculated for electrode area. This characteristic is typical for source of electromotive force. The RMS power density calculated for volume V of cellulose/SbSI NG (Fig. 6b) was determined by measuring the RMS voltage UL(RMS) for various load resistances RL (corrected for the Princeton EG&G 5110 input impedance of 100 MΩ). The presented characteristic was least square fitted (Fig. 6b) with theoretical dependence:
$$P_{L} (R_{L} ) = \frac{{R_{L} \cdot E^{2} }}{{V(Z_{S} + R_{L} )^{2} }},$$
where E = 30.0(55) mV is electromotive force and ZS = 2.90(11) MΩ is internal source impedance. The maximum power density output of cellulose/SbSI nanogenerator equals 41.5 nW/cm3 for load resistance comparable with source impedance.
Fig. 6

a Output voltage of cellulose/SbSI nanogenerator vs current density calculated for electrode area. b Power density calculated for volume of cellulose/SbSI vs load resistance for sound excitation (f = 175 Hz, Lp = 90 dB). Red curve presents fitted theoretical dependence. Description in the text

Figure 7 represents transient characteristic of open-circuit voltage generated in cellulose/SbSI nanogenerator under shock pressure excitation (the last peak is shown for enlarged time scale). When the air gun was turned on, the voltage increased sharply with time, passed through a maximum, and decreased to near-zero value. The recovery process was slower than rapid initial rise of open-circuit voltage (Fig. 7). The rise-time of the electromotive force is related to the shock front propagation time through the ferroelectric sample thickness (Shkuratov et al. 2010).
Fig. 7

Transient characteristic of open-circuit voltage generated in cellulose/SbSI nanogenerator under shock pressure excitation

Values of functional parameters (generated voltage, current, and power) of cellulose/SbSI nanogenerators presented in this article are hard to compare to data reported for piezoelectric papers (Kumar et al. 2011; Liao et al. 2014; Zhang et al. 2016). Different researchers applied various excitation methods (i.e., bending, pressing, and ultrasonic waves). In addition, the power of used excitation is unknown. But, one can recognize (Table 1) that parameters of nanogenerators made of novel cellulose/SbSI paper are comparable with those of other devices. Although, various materials for electrodes as well as their different geometries should be taken into serious consideration to improve functional parameters of cellulose/SbSI nanogenerators.
Table 1

Comparison of functional parameters of different piezoelectric nanogenerators based on cellulose fibers



Bacterial cellulose/BaTiO3



Exciting force

Sound wave

Pulse pressure



Ultrasonic waves







ISC (nA/cm2)






PS (nW/cm2)







175 Hz

30 bar

Polarized sample


40 kHz


This article

Zhang et al. (2016)

Liao et al. (2014)

Kumar et al. (2011)


Piezoelectric paper based on antimony sulfoiodide (SbSI) nanowires was presented for the first time. It is useful to construct nanogenerators for mechanical to electrical energy conversion. A simple device containing one pair of electrodes in sandwich configuration allows to generate open-circuit voltage of 24 mV and 2.5 V under sound excitation (f = 175 Hz, Lp = 90 dB) and shock pressure (30 bar, 144 m/s), respectively. Maximum output power of 0.21 nW/cm2 was registered for 0.05-mm-thick sheet of cellulose/SbSI.

Fabrication of cellulose/SbSI nanogenerators is low cost, simple, and effective. Functional parameters of these cellulose/SbSI nanogenerators should be improved in the future for optimized electrode configuration and device connection. Bending and vibration tests of these nanogenerators will be performed.

Cellulose/SbSI piezoelectric paper may also be useful to construct gas nanosensors and actuators.



This paper was partially supported by the Institute of Physics—Center for Science and Education, Silesian University of Technology and financial support for young scientists (BK/RIF/2017, 14/990/RGH17/0095, BKM-520/RIF/2017).


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Authors and Affiliations

  1. 1.Institute of Physics, Center for Science and EducationSilesian University of TechnologyKatowicePoland
  2. 2.Institute of Materials ScienceUniversity of SilesiaChorzowPoland
  3. 3.Department of Materials ScienceSilesian University of TechnologyKatowicePoland

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