Halide perovskites (HPs), with an excellent photoactive nature, dielectric, piezoelectric, ferroelectric, and pyroelectric properties, have been potential candidates for obtaining flexible nanogenerator-based self-powered sensors including light, pressure, and temperature. Additionally, the photo-stimulated dielectric, piezoelectric, and triboelectric properties of HPs make them efficient entrants for developing bimodal and multimode sensors to sense multi-physical signals individually or simultaneously.
Halide perovskite materials consist of three-dimensional ABX3-type crystal structures (Figure 1, crystal structure). In ABX3, A denotes the monovalent organic or inorganic cation (such as MA+ = CH3NH3+, FA = CH(NH2)2+ and Cs+), B represents the divalent cation (such as Pb2+, Sn2+, and Ge2+), and X is the halide anion (Cl, Br, I). In the crystal structure, cation A is coordinated with 12 neighboring X, and cation B is connected with 6 X anions, forming cuboctahedral and octahedral geometries, respectively. The structural formability of the 3D-ABX3 HPs and their stability were determined by the Goldschmidt tolerance factor (t) and the octahedral factors (μ) [1][2]. The tolerance factor, t = (rA + rX)/√2(rB + rX), where rA, rB, and rX represent the effective ionic radii of A, B, and X in the HP, respectively. The rB/rX is defined as an octahedral factor (μ) and is directly correlated with a BX6 octahedron, playing an important role in the multifunctional properties of HP materials. The tolerance factor values for HP materials were found to be within the 0.8–1.11 range, while the octahedral factor values were in the range of 0.44–0.90 [3][4]. The calculated t values for cubic, orthorhombic, and hexagonal structured HPs were 0.8 < t < 1.0, t < 0.8, and t > 1, respectively [2][5]. Numerous methods have been proposed to fabricate HP thin films, such as the one-step solution process, two-step sequential deposition, vapor deposition method, and vapor-assisted solution process [6][7][8][9]. Solution methods have been promoted due to simple and low-temperature fabrication ways and their compliance with flexible and large-scale devices [10][11].
Furthermore, the solution methods are promising to control crystalline formation better, leading to tunable properties at nano/micro-scale [12][13]. These HP-based materials have been considered to fabricate flexible nanogenerators owing to their impressive dielectric, ferroelectric, piezoelectric, and pyroelectric properties and beneficial features such as low-temperature and large-scale fabrication routes and controllable properties [14][15][16][17][18]. In particular, the dielectric and piezoelectric properties of HP-based materials are remarkable and nearly similar to those of ceramic materials [11][13][14][19][20][21]. Generally, the dielectric material is electrically an insulator and will readily polarize under an applied electric field. The ability of a material to store electrical energy can be estimated by its dielectric permittivity (εr) values. However, the dielectric loss factor describes the inefficiency of a material to hold the stored energy. Consequently, a material with a high loss factor cannot hold the charge completely indicating leaky nature of the sample. Therefore, materials with larger dielectric constant values and low dissipation factor values tend to generate higher output performance in nanogenerator applications because the nanogenerators are designed as part of capacitors [20]. Many researchers have demonstrated the dielectric properties of HP-based materials and also systematically examined the changes in dielectric properties of compositionally tuned HP materials [11][13][14][21]. The dielectric polarization mechanism in HP-based materials is nearly similar to well-known ceramic perovskite materials. The existing organic cation at the center of an HP-crystal structure (e.x., MA+ cation in MAPbI3) disorders under an applied field; thus, resulting in a dipolar polarization in HPs [11].
As depicted in Figure 2a, the most widely used MAPbI3 perovskite revealed an εr value of ~52 and low dissipation value of ~0.02 at an applied frequency of 100 kHz [19]. Moreover, FAPbI3 perovskite exhibited an improved dielectric property due to the presence of a larger cation (FA+) that has larger dipole momentum compared to that of MA+ cation [22]. In addition, the dielectric properties of HPs can be significantly enhanced by partial tuning of its composition. For example, the reported halide-doped MAPbI3 perovskite samples displayed a notable enhancement in dielectric properties upon halide doping (either Cl or Br) [14]. In particular MAPbI3-xClx displayed a high εr value of ~90.9. The improved property is not only because of improved grain size but also the existence of binary systems such as MAPbI3 and MAPbCl3 in the final film which led to interfacial polarization between two phases. Similarly, the Fe-incorporated MAPbI3 unveiled enhanced εr value of ~107 upon partial incorporation of Fe (x = 0.07) [13]. The improved dielectric properties promoted the enhancement in piezoelectric output performance of the MAPb1-xFexI3 based PENG. Furthermore, the lead-free Sn-based HP materials also possess high dielectric properties [23].
Figure 1. Schematic illustration of ABX3-type halide perovskite structure and their utility in nanogenerator-based self-powered sensing applications.
Figure 2. (a) Dielectric constants of various frequently used HP materials. Light intensity effect on frequency-dependent (b) dielectric constant and (c) dissipation factor of MAPbI3-PVDF composite films. (d) Light intensity effect on leakage current density of MAPbI3-PVDF composite films as a function of applied electric field. (b–d) Reprinted with permission from ref. [24], Copyright 2020, American Chemical Society.
HPs have been recognized as potential entrants in numerous research fields, including solar cells, LEDs, nanogenerators, and photodetectors. Among these, the nanogenerators are the recent application of HPs. They are highly sensitive to various external perturbations, such as pressure, temperature, and light. Hence, controlling the performance of a nanogenerator under external perturbations such as temperature and pressure predominantly enabled it to be used as a self-powered temperature or pressure sensor, respectively, without dependency on a battery. Additionally, illuminating nanogenerator significantly changes their output performance owing to the combined optoelectronic properties with piezoelectric property, or the triboelectric effect. Such light-stimulated performances of nanogenerators prominently enabled them to be used as self-powered photodetectors to detect the type of light or quantity of light intensity. This progress report briefly discussed the structural, piezoelectric, pyroelectric, and triboelectric properties of nanogenerators of HP materials. After that, we discussed the working mechanisms of several nanogenerators, including PENG, TENG, and PyENG as self-powered pressure and temperature sensors. We discussed the operation of PENG and TENG, as self-powered photodetectors under light illumination and present the possible underlying mechanisms to deliver the light-controlled outputs. Thereafter, we provided an overview of the exploration of using HP-based nanogenerators to sense various external factors such as pressure, temperature changes, and light. It is seen from the examples discussed above that when a nanogenerator is subjected to a controlled exposure to these external stimuli, continuous output voltage and current change linearly, which is a prerequisite for realizing reliable sensing systems. The recently emerging bimodal/multimodal sensing applications of HPs were also reviewed in addition to the single-mode sensor devices. We suggest the future projections of the research towards developing single-structure multimodal sensing devices.
Improving sensitivity, performance, and long-term stability of HPs is challenging despite many studies involving HPs as active sensing materials in self-powered nanogenerator-based sensors. Therefore, we identify potential directions and opportunities for future research. Recently, numerous methods, such as surface passivation, compositional tuning, fine-doping, and polymer composites, have been used to improve the air-stability of HP materials [23][24][16]. Furthermore, it has been demonstrated that the layered 2D-HPs have significantly good air and moisture stability than the 3D-HPs because of long-chain organic molecules [36][37]. Additionally, these 2D-HPs offer extremely high piezo/ferroelectric properties, helping to construct flexible, high-performance nanogenerators and reliable sensors with high sensitivity and stability [38]. Additionally, the development of eco-friendly HP material-based self-powered sensors has been highly prioritized to alleviate the environmental and human health risks. Additionally, extending the investigation to combine three or more properties may be helpful in developing trimodal/multimodal sensors to detect multiple physical signals simultaneously using a single-structure device without any signal interference. For example, our group has reported a single-structure TPS-fusion generator capable of harvesting multiple energy sources, such as thermal, mechanical, and light energies owing to the multiple properties of comprised MAPbI 3 material [39]. Finally, the flexible and stretchable self-powered sensing systems have significant potential to be for e-skin and wearable electronic device applications in the future. In this regard, considerable research should be conducted on HP materials to develop self-powered stretchable multifunctional devices that can continuously operate in harsh environs.
This entry is adapted from the peer-reviewed paper 10.3390/nanoenergyadv1010002