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Pla Harvesting
Pla Harvesting
A R T I C L E I N F O A B S T R A C T
Keywords: This study presents the development of a special class of electret known as thermoelectret, made with polylactic
3D printing acid (PLA), prepared via 3D printing technology followed by a heat-assisted corona discharged technique. We
Thermoelectret show that the bimodal surface polarity (i.e., ± 1 kV) is possible to achieve over the top and bottom surfaces of 3D
Self-powered pressure sensor
printed PLA thermoelectret that enable a wide range of potential applications, such as mechanical energy har
PLA
Health-monitoring
vesting to wearable biomedical sensors. Besides this, the enhanced surface potential leads to a giant longitudinal
piezoelectric coefficient (d33) of 350 ± 15 pC/N, which is typically 10 times higher than the best-known
piezoelectric polymer, polyvinylidene fluoride-trifluoro ethylene (PVDF-TrFE). To utilize this benefit, a 3D-
printed thermoelectret-based mechanical energy harvester (3D-TEH) has been developed that delivers an
outstanding power density of ⁓ 25 mW/m2, which makes it a suitable candidate for the self-power pressure
sensor. As a proof of concept, we have demonstrated that 3D-TEH is capable of recording the bone-joints mo
tions, coughing action, and human foot-pressure distribution that signify its potential application as a self-
powered bio-medical sensor.
1. Introduction PZT, BTO, and PZN-PT have a high piezoelectric coupling coefficient but
are unsuitable for flexible pressure sensors due to their brittleness and
Self-powered wearable pressure sensors and energy harvesters have rigidity [11]. Additionally, their toxicity limits their use in biomedical
gained considerable attention due to their applicability in various fields, devices. On the other hand, piezoelectric polymers like PVDF and
including health care monitoring [1–3], electronic prosthetic skin [4,5], PVDF-TrFE are flexible, lightweight, and biocompatible, making them
mechanical energy harvesting [6–9], and soft robotics [10]. Energy ideal for wearable pressure sensors [12]. However, they have limitations
harvesters, such as electret, triboelectric, and piezoelectric, harvest such as poor thermal fatigue, low Curie transition temperature, and a
mechanical energy and convert it into electric energy through different toxic synthesis route [13]. Moreover, piezoelectric polymer-based
operation modes and device structures. Piezoelectric materials, which pressure sensors require operation in resonance mode to obtain high
have microscopic dipoles, are commonly used as mechanical energy sensitivity, which presents challenges in circuit design and device
harvesters. Triboelectric energy harvesters, on the other hand, consist of fabrication [14]. Recently, a highly sensitive triboelectric pressure
materials with different surface potentials and generate electric charges sensor has been reported with a simple device fabrication process [15,
via their physical contact and separation. Electret energy harvesters 16]. However, the stability of the triboelectric pressure sensor is one of
utilize porous/voids/cellular structures in materials along with corona the major concerns due to frequent contact separation between the
discharge treatment. By employing various fabrication techniques and metal electrode and polymer surface [17]. In this context, recently,
device structures, polymer materials can be used for any of these energy electrets have gained lots of interest in fabricating pressure sensors due
harvesting methods. Piezoelectric materials are particularly favorable to their adequate mechano-sensitivity caused by ionized trapped air and
due to their simple device structures and self-powered functionalities. injected space charge within porous structures [18,19]. Based on the
They are frequently employed as pressure sensors and find applications fabrication process, there are various types of electrets available such as
in various industries [2,8]. Inorganic piezoelectric materials such as thermoelectret (DC electric field with temperature) [20,21],
* Corresponding author.
E-mail address: dmandal@inst.ac.in (D. Mandal).
https://doi.org/10.1016/j.sna.2023.114858
Received 2 August 2023; Received in revised form 25 October 2023; Accepted 18 November 2023
Available online 22 November 2023
0924-4247/© 2023 Elsevier B.V. All rights reserved.
D. Saini et al. Sensors and Actuators: A. Physical 365 (2024) 114858
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Fig. 2. Surface characterization of 3D printed PLA film. (a) 3D model (CAD) image, SEM image of (b) the top surface, and (c) the cross-sectional area, (d) 3D view of
AFM topography image (75 × 75 µm2) of 3D printed PLA film, (e) Water contact angle (WCA) measurement of 3D printed PLA film, (f) XPS survey scan, and high-
resolution XPS spectra of (g) C 1s and (h) O 1s.
IC=O–C /ICH2 –CH3 ~ 0.72). In contrast, it decreases in the case of the bot neat PLA film, whereas it is 1.2 for corona discharged PLA film (Fig. 4a),
tom surface (i.e., IC=O–C /ICH2 –CH3 ~ 0.62). This resembles that after which denotes the significant change in the orientation of C–O–C bond is
corona discharge, photoelectron counts from oxygen species are noted due to corona discharge treatment. The absorption band at
increased on the top surface, while it decreases for the bottom surface in 1265 cm− 1 corresponds to the vibration mode of δ(C–H) + ν(C–O–C)
comparison to the neat PLA surface. This supports the fact that dipole attributed to the crystalline band for PLA [59,60]. Thus, the appearance
(–C––O) orients along the electric field direction due to corona discharge of this band (Fig. 4a) after corona discharge treatment signifies the
treatment (Fig. 3b(ii)). Similarly, the same fact can also be observed generation of crystalline nature [58,60]. The bands at 1360 cm− 1 and
from the O 1s signal (Fig. 3d), if one considers the peak ratio between 1401 cm− 1 are assigned to the crystalline and amorphous characteristics
C––O and C–O species of the untreated and treated PLA surfaces. of the PLA, respectively [61]. After corona discharge treatment, the
appearance of the band at 1360 cm− 1 and the disappearance of the band
To examine the influence of corona discharge treatment on electro
at 1401 cm− 1 (Fig. 4b) signify the improvement of the degree of crys
active phases and polarization states of the 3D printed films at different
tallinity. These observations support the fact that polar bonds in the
temperatures, Fourier transform infrared spectra (FTIR) (Fig. 4a-b) were
polymer chain are getting oriented in a particular direction due to the
recorded. The change in the shape of the vibrational band between 840
application of the electric field and supplied thermal energy. It is further
and 880 cm− 1 is annotated as an increase in the degree of crystallization.
confirmed by the retained behavior of the vibrational bands when the
The characteristic vibrational band at 871 cm− 1 is attributed to C–C
electric field is applied without heat treatment (Fig. S3). The absorbance
backbone stretching, which overlaps with the vibrational band at
band, which commonly lies within the ranges of 1810 – 1710 cm− 1, is
860 cm− 1 assigned for skeletal stretching [57,58]. With the increase in
temperature, the peak shifts from 871 to 867 cm− 1, and becomes the signature of C– –O stretching, which is primarily responsible for the
significantly narrower, denoting the crystallization process takes place piezoelectric behavior of PLA [56,58]. The shifting of the C–O –
[58]. The intensity ratio of symmetric (1088 cm− 1) and asymmetric stretching band from 1757 to 1749 cm− 1 indicates the change in the
(1184 cm− 1) stretching bands of the C–O–C group (Iνsy /Iνas ) is 0.8 for orientation (Fig. 4b) upon the corona discharge treatment [62]. It is
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Fig. 3. Formation of thermoelectret with corona discharge treatment. (a) Schematic of the printed PLA film (i) before, and (ii) after corona discharge treatment, (b)
Schematic of PLA polymer chain conformation (i) before, and (ii) after corona discharge treatment, High-resolution XPS spectra (c) C 1s, and (d) O 1s of top and
bottom surface of untreated and corona discharge treated PLA film.
noteworthy to mention that the overall FTIR spectra of corona discharge 50◦ to 110◦ C) by aligning the dipoles along the direction of the field
PLA specimen are similar to the electrospun PLA fiber [57,58], which [18]. To investigate how polarization changes with the electric field at
specifies that in both cases electric field plays an essential role in ori different temperatures, P-E loop measurements are performed. The
enting the C– –O dipoles and polarization of the polymer chain. This thermoelectret material displayed a gradual increase in remanent po
supports the fact that 3D-printed PLA film exhibits thermoelectret larization (Pr) as the temperature rose, proving that the 3D-printed PLA
behavior after corona discharge treatment. film does not exhibit ferroelectric behavior (as depicted in Fig. 4d) [40].
We have conducted the XRD measurement of the thermoelectret to In contrast, ferroelectric materials, such as P(VDF-TrFE), shown in
investigate the degree of crystallinity (Xc), which is confirmed by the Fig. 4d for comparison, demonstrate a gradual decrease in remanent
crystalline characteristics of PLA thermoelectret. The XRD pattern polarization with increasing temperature [20]. It is worth noting that
(Fig. 4c) of an untreated PLA thermoelectret displays a broad, amor the micro-pores within the electret material act as micro-dipoles when
phous halo, whereas a corona-treated PLA thermoelectret illustrates subjected to an electric field [66,67]. Typically, the production of
several intense peaks. In particular, peaks at (2θ) 15◦ , 16.7◦ , 19◦ , 29◦ electrets involves artificially trapping charges within the larger voids of
and 31◦ are characteristic of the α phase, corresponding to the (010), porous polymer structures to create oriented quasi-dipoles [68,69]. In
(110)/(200), (203), (216) and (0010) plane respectively [63,64]. this specific case, electric charges were injected into the porous
Whereas the peaks at (2θ) 25.1◦ , 27.7◦ , and 31.2 imply the presence of β 3D-printed PLA film using corona discharge treatment. This treatment
crystalline phase [63,65]. Thus, it is concluded that after corona induces the orientation of -C– –O dipoles and stabilizes the trapped
discharge treatment, a mixture of α and β crystallites are developed (Xc charges, which occurs above the glass transition temperature (for
~ 54%) in PLA thermoelectret film. example, within the temperature range of 50–110 ◦ C). All of these
The thermoelectret material generates polarization when exposed to findings support the thermoelectret behavior observed in the 3D-printed
a strong electric field (~MV/m) and varying temperatures (ranging from PLA film.
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D. Saini et al. Sensors and Actuators: A. Physical 365 (2024) 114858
Fig. 4. FTIR spectra of untreated and corona-discharge treated PLA films in the absorption range (a) 2000 – 800 cm− 1, (b) 1800 – 1350 cm− 1, (c) XRD patterns of
untreated and corona-discharged treated 3D-printed thermoelectret, Inset is showing the enlarged view of the 2θ ~24–33◦ range. (d) Variation in remanent po
larization (Pr) with temperature for thermoelectret (non-ferroelectric) and PVDF-TrFE (ferroelectric) samples.
3.3. Surface potential of 3D printed PLA thermoelectret molecules. Later, the surface charge decays over time due to its inter
action with surroundings [31,33], which causes decay in surface po
To examine the surface potential of 3D printed thermoelectret PLA tential [68], while the trapped charge inside cavities stays uninterrupted
film, a probe of the electrostatic voltmeter is placed just above the due to the unavailability of atmospheric air, and these trapped charges
surface of PLA films, which is kept on a movable x-y stage as illustrated exhibit the stable surface potential. In addition, we have encapsulated
in Fig. 5a. The top and bottom surfaces of the corona discharge treated the fabricated thermoelectret film into PDMS, which restricts its inter
PLA films at different temperatures from 30◦ to 110◦ C are labeled as T# action with atmospheric air as well. Earlier work on PLA electret shows
and B#, Where T, B, and # represent the top surface, bottom surface, sharp decay of the surface potential in a few hours [55,59]. Here, in this
and temperature (30 – 110 ◦ C) respectively. The measured surface po work, the porous structure of PLA film is responsible for stable surface
tential of the top and bottom surfaces of corona-treated PLA films at potential, which traps charges effectively. To realize the variation in the
different temperatures are displayed in Fig. 5b. It epitomizes that surface potential of PLA film after corona discharge, a quantitative
initially, the surface potential is lower (~ ± 0.1 kV) at RT; later, it in measurement of surface potential is performed at different positions on
creases as the temperature rises and reached optimum magnitude (i.e., the top surface of PLA film before and after corona discharge. The
~ ± 1 kV) in the temperature range of 60 – 70 ◦ C. However, when the resultant surface potential mapping before and after corona discharge
corona discharge temperature is reached above 70 ◦ C, then the surface treatment is shown in Fig. 5e(i) and 5e(ii), respectively. The surface
potential starts decreasing. The enhancement of surface potential near potential mapping shows an almost uniform surface potential distribu
60 ◦ C might be due to the relaxation of polymer chains that start at the tion on the film surface after corona discharge. The influence of the
glass transition temperature (58 ◦ C, Fig. S4), which allows the charge obtained high surface potential in energy harvesting performance can be
carriers to trap within the 3D-printed porous film. Also, it polarizes the realized from the open circuit voltage, short circuit current, and giant
surface dipoles (–C– –O) along the electric field direction. However, at piezoelectric coefficient, which is almost three times higher after corona
higher temperatures (i.e., > 70 ◦ C), the excessive dipole relaxation discharge treatment. To understand the experimentally observed higher
speeds up the randomization of –C– –O dipoles due to high rotational surface potential on corona-treated PLA films, finite element analysis is
energy that reduces the surface potential [57]. The surface potential performed (Fig. 5f). The finite element technique is used to optimize the
behavior of 3D printed PLA film is analogous to earlier reports on suitable void size for which the surface potential would be maximum.
thermoelectret [30]. Further, to investigate the stability of the surface Further, the surface potential was mapped, which shows excellent sur
potential of the corona-discharged PLA films, the surface potential decay face potential in comparison to untreated 3D printed film in terms of
is studied over a long period of time (Fig. 5c-d). It is observed that the magnitude and distribution.
surface potential decreases initially, but it is constant after a specific
duration (i.e., 14 days), and no further decay of surface potential with 3.4. Performance of 3D-TEH
time is observed (as recorded again after 45 days). At the time of corona
discharge, air trapped inside the cavities is ionized and acts as macro The mechanism diagram for mechanical energy harvesting and
scopic dipoles, while atmospheric air near the electret surface gets pressure sensing of the 3D-TEH under mechanical pressure is depicted
ionized and resides on the surface due to its interaction with surface schematically in Fig. 6a [70]. The corona discharging treatment
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D. Saini et al. Sensors and Actuators: A. Physical 365 (2024) 114858
Fig. 5. The surface potential behavior of 3D printed thermoelectret PLA film treated with corona discharge at different temperatures (Mean ± SD; N = 16). (a)
Schematic of surface potential measurement set-up, (b) Variation in the surface potential of top and bottom surfaces, (c) Study of variation in surface potential over
time, (d) Behavior of surface potential over time for the colored region shown in Figure c, (e) Surface potential distribution mapping on the top surface of PLA film
before (i), and after (ii) corona discharge treatment, (f) Finite element analysis for the surface potential of 3D printed thermoelectret.
produces positive and negative charges (macro-dipoles) within the positive output voltage is observed (Fig. 6a). Further, as the mechanical
surface of internal cavities, which are separated by the height of cavities, force is released, the distance between the positive and negative is
which induces dipole moment inside the cavities. Additionally, the starting to increase that speed up the net polarization change in the
–C––O polar groups tend to orient along the electrical field direction, opposite direction, which promotes the flow of electrons from the bot
contributing to a significant polarization. Thus, corona discharge tom to the top electrode; hence a negative output voltage is observed.
treatment with temperature excites net polarization due to a cooperative Therefore, as a result of the mechanical compression and release action,
response from molecular dipoles (–C– –O) of PLA and micro dipoles the corresponding voltage signal is produced, which can be used to
monitor the applied force/pressure on the 3D-TEH. The output re
within the internal cavities. The generated net polarization on the
sponses (open circuit voltage, Voc ⁓ 3 ± 0.2 V and short circuit current
thermoelectret surface accelerates the formation of charges (of opposite
density, Isc ⁓ 4.7 ± 0.25 mA/m2) from 3D-TEH are represented in
nature) at the surface of the thermoelectret, which engenders the
Figs. 6b and 6c when 10 N of external force is applied with 4 Hz of
accumulation of positive and negative charges on the top and bottom
frequency[71]. The obtained electrical output (i.e., 0.9 ± 0.1 V of
surfaces of electrodes. As the mechanical force is applied to the ther
peak-to-peak voltage response) from control 3D-TEH generates due to
moelectret, it compresses, and the distance between the positive and
the electret behavior of 3D printed porous film and soft piezoelectric
negative charges residing at the thermoelectret surface has reduced that
behavior of PLA (Fig. 6b) [62,72]. After corona discharge, the electrical
leads to a change in net polarization along the thickness direction, which
output increases ⁓ 300% compared to the control 3D-TEH due to uni
facilitates the flow of electrons from top to bottom electrode, hence a
formly oriented charged micro-dipoles. The calculated d33 of
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D. Saini et al. Sensors and Actuators: A. Physical 365 (2024) 114858
Fig. 6. The energy harvesting performance of 3D-TEH. (a) Schematic of the energy harvesting and pressure sensing mechanism of the 3D-TEH, (b) The obtained
open-circuit voltage (Voc), (c) Short circuit current density (Isc), and (d) Response time of the fabricated 3D-TEH. (e) Obtained Voc, (Isc), and power density at various
load resistance (RL) range 10 kΩ - 100 MΩ, the inset indicates the operated 9 green LEDs directly connected to the 3D-TEH (Video S1), (f) The commercial capacitor
charging performance of fabricated 3D-TEH using the circuit diagram shown in the inset.
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D. Saini et al. Sensors and Actuators: A. Physical 365 (2024) 114858
Fig. 7. Biomechanical signal monitoring using 3D-TEH. Output voltage response with (a) finger bending, (b) elbow bending, (c) knee bending, and (d) Measured
voltage output response of repeated coughing actions and (e) corresponding short-time Fourier transform (STFT) spectrogram, recorded with 3D-TEH, (f) Output
voltage responses of the fabricated 3D-TEH for normal walking while placed at different locations (Middle, Heel-Pad, and Met-Head) on the human foot.
∫
Idt obtained power is capable of powering up nine green LEDs without any
thermoelectret PLA film is ⁓ 350 ± 15 pC/N, estimated from d33 = F ,
external support of batteries (inset of Fig. 6e and Video S1). The per
where I is the current amplitude within the time interval dt upon the
formance of 3D printed thermoelectret was further compared with other
application of applied external force (F) [3,6], which is ⁓ 333% higher
reported energy harvesting work where nanogenerators are developed
in comparison to the control 3D printed film (Fig. S5). It reveals that due
using 3D printing and other techniques, as provided in Table S3. The
to thermoelectret properties, a transverse electromechanical response,
energy harvester performance was compared on the basis of power
governed by the d33 coefficient, significantly dominates over the shear
density and the performance factor, which is defined as generated
piezoelectricity, as it usually appears in PLA (Table S1). The fast
piezo-voltage (peak to peak) per unit applied pressure (kPa). The
response time of ~ 7 ms (Fig. 6d) illustrates that 3D-TEH also has the
comparative results show a better or comparable performance of
capability to be used as a potential tactile sensor. To determine the
3D-printed thermoelectret than most of the earlier reported results. To
maximum efficiency of the 3D-TEH instantaneous voltage drop (Voc) and
examine the self-powered capabilities of 3D-TEH, an electronic circuit
current density (Isc) over various load resistances ranging from 10 kΩ to
consists of a bridge diode rectifier, and a commercial capacitor is con
100 MΩ is demonstrated under an external force of 10 N (Fig. 6e). Here,
nected to 3D-TEH as shown in the schematic of the circuit diagram (inset
Voc increases as the load resistance increases, while Isc decreases due to
of Fig. 6f). The 3D-TEH is capable of charging up the commercial ca
the building up of resistive load and get saturated at infinitely large
pacitors of 1, 2.2, and 4.7 µF up to 1.5, 1.4, and 1.1 V, under the cyclic
resistance. The electrical density (P) is calculated from Voc across load
load of 10 N within the period of 20–40 s with the time constant
resistance (RL) using the formula P = AR
Voc
L
, where A is the effective device (required time to attain 63% of its steady-state charging voltage) of 13,
area. The estimated output power density is ⁓ 25 mW/m2 at RL 1 MΩ. It 20 and 23 s, respectively as illustrated in Fig. 6f. It reveals the fast power
suggested that the maximum output power lies at the same load resis supply of the fabricated 3D-TEH. The fatigue test is performed that
tance where Voc and Isc intersect each other, as evident from Fig. 6e. The shows till 30,000 cycles, a stable current response is sustained,
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D. Saini et al. Sensors and Actuators: A. Physical 365 (2024) 114858
4. Conclusion
Fig. 10. (a) Schematic of the 3D-TEH sensor array with imparted PLA slab with shaped “I, N, S, and T”, (b) pressure mapping using the 3D-TEH sensor array.
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The authors declare that they have no known competing financial states of Boswellia Glabra and ZnO-Boswellia Glabra mixtures and their
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nano-pressure sensor, Macromol. Rapid Commun. 32 (2011) 831–837. [46] E.J. Curry, K. Ke, M.T. Chorsi, K.S. Wrobel, A.N. Miller, A. Patel, I. Kim, J. Feng,
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detection and energy harvesting integrated magnetoelectric sensor with flexibility D. Nguyen, Biodegradable piezoelectric force sensor, Proc. Natl. Acad. Sci. U. S. A.
and heat resistance based on Polylactide/VB2 composites and FeCoV, Adv. Mater. 115 (2018) 909–914.
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[14] K. Uchino, Ferroelectr. Devices 2nd Ed. 2009, 297. stable cantilever for vibration energy harvesting applications, Adv. Sustain. Syst. 1
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films, Nano Lett. 12 (2012) 3109–3114. electret-based soft hybrid generator for human body applications, Smart Mater.
[16] Y. Kim, X. Wu, J.H. Oh, Fabrication of triboelectric nanogenerators based on Struct. 28 (2019), 104003.
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[17] X. Pu, S. An, Q. Tang, H. Guo, C. Hu, Wearable triboelectric sensors for biomedical Conf. Proc. 2148 (2019), 030052.
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[18] S. Gong, B. Zhang, J. Zhang, Z.L. Wang, K. Ren, Biocompatible poly(lactic acid)- Investigation of thermo-mechanical, chemical and degradative properties of PLA-
based hybrid piezoelectric and electret nanogenerator for electronic skin limonene films reinforced with cellulose nanocrystals extracted from Phormium
applications, Adv. Funct. Mater. 30 (2020) 1908724. tenax leaves, Eur. Polym. J. 56 (2014) 77–91.
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[51] J. Xu, Y. Hou, Z. Lian, Z. Yu, Z. Wang, H. Yu, Bio-inspired design of bi/
tridirectionally anisotropic sliding superhydrophobic titanium alloy surfaces,
Nanomaterials 10 (2020) 2140. Mr. Dalip Saini is pursuing his Ph.D. from the Department of
[52] J. Kowalonek, I. Vuković-Kwiatkowska, D. Moszyński, H. Kaczmarek, Surface Quantum Materials and Devices at the Institute of Nano Sci
properties of poly(lactic acid)/polyacrylate semi-interpenetrating networks – effect ence and Technology (INST), Mohali, India. He received his M.
of UVC radiation, Polym. Degrad. Stab. 131 (2016) 71–81. Sc. and B.Sc. degrees in physics from the Central University of
[53] M.V. Paranjape, S.A. Graham, H. Patnam, P. Manchi, J.S. Yu, 3D printed Haryana, India, in 2018 and the University of Rajasthan, India,
bidirectional rotatory hybrid nanogenerator for mechanical energy harvesting, in 2016, respectively. His research interest mainly includes 3D
Nano Energy 88 (2021), 106250. printing electret, energy harvesting using piezo-, pyro- tribo-,
[54] A. Guzhova, M. Galikhanov, Charge depth in polylactic acid electret filled with fine and magneto-electric nanogenerator, self-powered for human-
filler, Bulg. Chem. Commun. 47 (2015) 103–108. health monitoring, security and motion-detection, wirelessly
[55] R.W. Crowe, J.K. Bragg, Thomas, G. Virginia, Space charge formation and the real-time data transmission, and IOT based smart application
townsend mechanism of spark breakdown in gases, Phys. Rev. 96 (1954) 10–14.
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research, Curr. Sci. 85 (2003) 443–453.
[57] A. Sultana, S.K. Ghosh, V. Sencadas, T. Zheng, M.J. Higgins, T.R. Middya,
D. Mandal, Human skin interactive self-powered wearable piezoelectric bio-e-skin
by electrospun poly-l-lactic acid nanofibers for non-invasive physiological signal
monitoring, J. Mater. Chem. B. 5 (2017) 7352–7359. Mr. Ajay Kumar is a doctorate candidate at INST, Mohali,
[58] C. Ribeiro, V. Sencadas, C.M. Costa, J.L. Gómez Ribelles, S. Lanceros-Méndez, India. Prior to that, he completed M. Sc. (2018) and B. Sc.
Tailoring the morphology and crystallinity of poly(L-lactide acid) electrospun (2016) in Physics (H) from SLIET (CFTI) Sangrur, India, and
membranes, Sci. Technol. Adv. Mater. 12 (2011), 015001. Ramjas College, Delhi University, respectively. His research
[59] G. Kister, G. Cassanas, M. Vert, Effects of morphology, conformation and interest is to study the physics of ferro,-piezo- and pyro-electric
configuration on the IR and Raman spectra of various poly(lactic acid)s, Polymer materials (polymer and 2D materials based) and their device
39 (1998) 267–273. fabrication for the end application
[60] H. Urayama, S.-I. Moon, Y. Kimura, Macro microstructure and thermal properties
of polylactides with different L- and D-unit sequences: importance of the helical
nature of the L-sequenced segments, Macromol. Mater. Eng. 288 (2003) 137.
[61] J. Zhang, H. Tsuji, I. Noda, Y. Ozaki, Structural changes and crystallization
dynamics of poly(L-lactide) during the cold-crystallization process investigated by
infrared and two-dimensional infrared correlation spectroscopy, Macromolecules
37 (2004) 6433–6439.
[62] A. Farahani, A. Zarei-Hanzaki, H.R. Abedi, L. Tayebi, E. Mostafavi, Polylactic acid
piezo-biopolymers: chemistry, structural evolution, fabrication methods, and tissue
engineering applications, J. Funct. Biomater. 12 (2021) 71. Dr. Hari Krishna Mishra has received his Ph.D. degree from
[63] L. Su, J. Zou, S. Dong, N. Hao, H. Xu, Influence of different β-nucleation agents on IISER Mohali, India, in 2023. He has carried out his doctorate
poly(L-lactic acid): Structure, morphology, and dynamic mechanical behavior, RSC work in INST, Mohali, India. He received his M.Sc. (2016) and
Adv. 7 (2017) 55364–55370. B.Sc.(2014) degrees in Physics from CSJM University, Kanpur,
[64] K. Takahashi, D. Sawai, T. Yokoyama, T. Kanamoto, S.H. Hyon, Crystal India, respectively. His research interest is focused on
transformation from the α- to the β-form upon tensile drawing of poly(L-lactic designing polymer-based nanomaterials and 2D transition
acid), Polymer 45 (2004) 4969–4976. metal dichalcogenides (TMDCs) of piezo-, pyro-, and ferro-
[65] H.M. De Oca, I.M. Ward, Structure and mechanical properties of poly(L-lactic acid) electric properties for the mechanical energy harvester, self-
crystals and fibers, J. Polym. Sci. B Polym. Phys. 45 (2007) 892–902. powered devices, energy storage, and physiological signal
[66] S.K. Ghosh, M. Xie, C.R. Bowen, P.R. Davies, D.J. Morgan, D. Mandal, A hybrid monitoring.
strain and thermal energy harvester based on an infra-red sensitive Er3+ modified
poly(vinylidene fluoride) ferroelectret structure, Sci. Rep. 7 (2017) 16703.
[67] S. Bauer, R. Gerhard-Multhaupt, G.M. Sessler, Ferroelectrets: soft electroactive
foams for transducers, Phys. Today 57 (2004) 37–43.
[68] A. Guzhova, T. Yovcheva, A. Viraneva, Study of polylactic acid corona electrets,
Bulg. Chem. Commun. 47 (2015) 115–120.
[69] A.A. Guzhova, M.F. Galikhanov, Y.A. Gorokhovatsky, D.E. Temnov, E. Dr. Varun Gupta has received his Ph.D. degree from IISER
E. Fomicheva, E.A. Karulina, T.A. Yovcheva, Improvement of polylactic acid Mohali, India, in 2023. He has carried out his doctorate work in
electret properties by addition of fine barium titanate, J. Electro 79 (2016) 1–6. INST, Mohali, India. He has received his BS-MS degree in
[70] X. Zhang, P. Pondrom, G.M. Sessler, X. Ma, Ferroelectret nanogenerator with large physics (2016) from IISER Bhopal, India. His research interest
transverse piezoelectric activity, Nano Energy 50 (2018) 52–61. is focused on polymer-based nanomaterials with piezo-, pyro-
[71] S.K. Ghosh, D. Mandal, High-performance bio-piezoelectric nanogenerator made and ferro-electric properties for mechanical, thermal energy
with fish scale, Appl. Phys. Lett. 109 (2016), 103701. harvesters, and self-powered devices. During this PhD tenure,
[72] Z. Hanani, I. Izanzar, S. Merselmiz, T. El Assimi, daoud mezzane, M. Amjoud, he explored the SPM techniques to understand nanoscale
H. Uršič, U. Prah, J. Ghanbaja, I. Saadoune, M. Lachini, M. Spreitzer, D. Vengust, electromechanical properties.
M. El Marssi, Z. Kutnjak, I.A. Luk’yanchuk, M. Gouné, A flexible self-poled
piezocomposite nanogenerator based on H2(Zr0.1Ti0.9)3O7 nanowires and
polylactic acid biopolymer, Sustain. Energy Fuels 31–33 (2022).
[73] Z. Gao, X. Wang, Y. Zhao, J. Jin, G. Wang, S. Gao, Piezoelectric-based smart bone
plate for, J. Shanghai Jiaotong Univ. (Sci. ) 27 (2022) 561–569.
[74] J.M. Kaufman, A.T. Masc, Y. Fossat, Acoustic analysis and prediction of type 2
diabetes mellitus using smartphone-recorded voice segments, MAYO Clin. Proc.
Mr. Bidya Mondal is a PhD candidate at the Institute of Nano
Digit. Heal. 1 (2023) 534–544.
Science and Technology (INST), India. In prior to that, he ob
[75] S.K. Ghosh, D. Mandal, Bio-assembled, piezoelectric prawn shell made self-
tained B.Sc. and M.Sc. degrees in Physics from the University of
powered wearable sensor for non-invasive physiological signal monitoring, Appl.
Burdwan in 2018 and the Indian Institute of Technology (In
Phys. Lett. 110 (2017), 123701.
dian School of Mines) Dhanbad in 2020, respectively. His
[76] P. Piirila, A.R.A. Sovijarvi, Objective assessment of cough, Eur. Respir. J. 8 (1995)
research interest includes piezoelectric and photovoltaic-based
1949.
energy harvesting.
[77] D.L. Riddle, M. Pulisic, P. Pidcoe, R.E. Johnson, Risk factors for plantar fasciitis: a
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S. Ulbrecht, P.R. Cavanagh, Plantar pressures in diabetic patients with foot ulcers
which have remained healed, Diabet. Med. 26 (2009) 1141–1146.
[79] F. Crawford, M. Inkster, J. Kleijnen, T. Fahey, Predicting foot ulcers in patients
with diabetes: a systematic review and meta-analysis, Qjm 100 (2007) 65–86.
[80] J. Fletcher, Nurs Times., The foot in diabetes. 92 (1996) 88–90.
[81] S.A. Bus, Innovations in plantar pressure and foot temperature measurements in
diabetes, Diab. Metab. Res. Rev. 32 (2016) 221–226.
[82] Y.C. Lai, H.S. Lin, H.F. Pan, W.N. Chang, C.J. Hsu, J.H. Renn, Impact of foot
progression angle on the distribution of plantar pressure in normal children, Clin.
Biomech. 29 (2014) 196–200.
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D. Saini et al. Sensors and Actuators: A. Physical 365 (2024) 114858
Ms. Zinnia Mallick is a PhD candidate at the Department of Prof. Dipankar Mandal received his PhD in 2008 from BTU
Quantum Materials & Devices at the Institute of Nano Science Cottbus (currently known as BTU Cottbus-Senftenburg), Ger
and Technology, Mohali, India. Prior to that, she obtained her many. Prior to that, he obtained his MTech in Materials Science
MSc in Physics (2017) from Presidency University, Kolkata. and Eng. (2004) and MSc in Physics (2002) from IIT Khar
Her research interest includes the study of nanoscale piezo, agpur, India, and Jadavpur University, Kolkata, India, respec
pyro and ferroelectric properties of materials, piezo and pyro tively. He is currently working as a Scientist at the Institute of
electric sensors, and perovskite photovoltaics. Nanoscience and Technology (INST), Mohali, India. He was an
Assistant Professor in the Department of Physics, Jadavpur
University Kolkata, India from 2008 to 2017. His research in
terests include the synthesis of advanced multifunctional ma
terials, flexible electronics, piezo-, tribo-, pyro-, ferro-and
flexo-electric materials, organic photovoltaics, and electro-
spinning systems for the development of new-generation
nanofiber fabrication, 3D printing, smart textiles, and AI/ML aided non-invasive bio-
sensors for healthcare monitoring, and designing mechanical and thermal energy har
vesters for self-powered devices and IoTs
14