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Organic–inorganic hybrid perovskites (OIHPs) with dielectric switching functions have aroused comprehensive scientific interest, benefitting from their promising applications in sensors and information storage. However, to date, most of these materials discovered thus far possess a single function and are limited in their applicability, failing to meet the requirements of diverse applications. Moreover, the discovery of these materials has been largely serendipitous. Building multifunctional OIHPs with dielectric switching and semiconductors remains a daunting task. In this context, by introducing [C7H16N]+ as cations and in combination with lead halide with semiconducting properties, two OIHPs [C7H16N]PbI3 (1) and [C7H16N]PbBr3 (2) ([C7H16N]+ = (cyclopropylmethyl) trimethylammonium) have been successfully designed. They have dielectric switching properties close to 253 and 279 K and semiconducting behavior with band gaps of 2.67 and 3.22 eV. The phase transition temperature increased by 26 K through halogen substitution. In summary, our findings in this study provide insights into the application of the halogen substitution regulation strategy and open up new possibilities for designing perovskite semiconductors with dielectric switching functionality. [ABSTRACT FROM AUTHOR]

Abundant chemical diversity and structural tunability make organic–inorganic hybrid perovskites (OIHPs) a rich ore for ferroelectrics. However, compared with their inorganic counterparts such as BaTiO3, their ferroelectric key properties, including large spontaneous polarization (Ps), low coercive field (Ec), and strong second harmonic generation (SHG) response, have long been great challenges, which hinder their commercial applications. Here, a quasi-one-dimensional OIHP DMAGeI3 (DMA = Dimethylamine) is reported, with notable ferroelectric attributes at room temperature: a large Ps of 24.14 μC/cm2 (on a par with BaTiO3), a low Ec below 2.2 kV/cm, and the strongest SHG intensity in OIHP family (about 12 times of KH2PO4 (KDP)). Revealed by the first-principles calculations, its large Ps originates from the synergistic effects of the stereochemically active 4s2 lone pair of Ge2+ and the ordering of organic cations, and its low kinetic energy barrier of small DMA cations results in a low Ec. Our work brings the comprehensive ferroelectric performances of OIHPs to a comparable level with commercial inorganic ferroelectric perovskites. The authors report on a quasi-one-dimensional organic-inorganic hybrid perovskite, DMAGeI3 (DMA = Dimethylamine), with notable ferroelectric attributes at room temperature including large spontaneous polarisation, low coercive field, and strong second harmonic generation response. [ABSTRACT FROM AUTHOR]

The tunable structure, abundant raw materials, and ease of preparation have made molecular dielectric crystals popular for use in device design. In spite of this, some known molecular switching materials have a low phase transition temperature and a low dielectric constant, which limit their applications. Therefore, designing and synthesizing molecular‐based phase transition compounds with high phase transition temperature and superior properties is especially important. In this work, we use 3‐chloropropan‐1‐ammonium hydrochloride and SbCl3/SbBr3 inorganic salts as building blocks to synthesize compounds (CPA)2(BPA)2Sb2Br10 (1) (CPA=3‐chloropropan‐1‐ammonium, BPA=3‐bromopropan‐1‐ammonium) and (CPA)2Sb2Cl8 (2). Compound 1 has a high phase transition temperature (407.45 K). Dielectric measurements and differential scanning calorimetry (DSC) confirm the structural phase transition in compound 1, and no fatigue decay is observed after several dielectric cycles. In addition, compounds 1 and 2 possess semiconductor properties. The findings of this study provide new directions for the design and application of multifunctional molecular dielectric materials. [ABSTRACT FROM AUTHOR]

Molecular ferroelectrics have gradually aroused great interest in both fundamental scientific research and technological applications because of their easy processing, light weight and mechanical flexibility. Hybrid organic–inorganic perovskite ferroelectrics (HOIPFs), as a class of molecule-based ferroelectrics, have diverse functionalities owing to their unique structure and have become a hot spot in molecular ferroelectrics research. Therefore, they are extremely attractive in the field of ferroelectrics. However, there seems to be a lack of systematic review of their design, performance and potential applications. Herein, we review the recent development of HOIPFs from lead-based, lead-free and metal-free perovskites, and outline the versatility of these ferroelectrics, including piezoelectricity for mechanical energy-harvesting and optoelectronic properties for photovoltaics and light detection. Furthermore, a perspective view of the challenges and future directions of HOIPFs is also highlighted. [ABSTRACT FROM AUTHOR]

In order to meet the needs of social development, increasing research attention has been paid to multifunctional molecular-based phase-transition materials. The traditional phase-transition materials with a single functional property can be transformed into magnificent ones by adding additional functional properties—for instance photoluminescence and magnetic order— because having two or more functional properties simultaneously greatly broadens the fields of their applications. At present, there are very few multifunctional phase-transition materials showing excellent performance, and the crystal structure design and performance optimization of materials still need to be studied in depth. Herein, we report the development of two organic–inorganic hybrid materials: (MBA)2ZnI4 (1, MBA = 4-methoxybenzylammonium) with switchable dielectricity and a high phase-transition temperature (Tc = 359.55 K), and (MBA)2ZnBr4 (2) with green luminescence (λexc = 314 nm) and nonlinear optical properties (0.75× KDP). A two-dimensional (2D) fingerprint analysis of the Hirshfeld surface plots revealed a significant difference between the hydrogen-bonding interaction before the phase transition and that afterwards. The two compounds were further verified, from energy band structure calculations, to be direct-band-gap semiconductors. In conclusion, this work has provided a viable strategy, involving the application of chemical modifications, for designing various functional materials. [ABSTRACT FROM AUTHOR]

Molecular ferroelastics have received particular attention for potential applications in mechanical switches, shape memory, energy conversion, information processing, and solar cells, by taking advantages of their low‐cost, light‐weight, easy preparation, and mechanical flexibility. The unique structures of organic–inorganic hybrid perovskites have been considered to be a design platform for symmetry‐breaking‐associated order–disorder in lattice, thereby possessing great potential for ferroelastic phase transition. Herein, we review the research progress of organic–inorganic hybrid perovskite ferroelastics in recent years, focusing on the crystal structures, dimensions, phase transitions and ferroelastic properties. In view of the few reports on molecular‐based hybrid ferroelastics, we look forward to the structural design strategies of molecular ferroelastic materials, as well as the opportunities and challenges faced by molecular‐based hybrid ferroelastic materials in the future. This review will have positive guiding significance for the synthesis and future exploration of organic–inorganic hybrid molecular ferroelastics. [ABSTRACT FROM AUTHOR]

Two-dimensional (2D) organic–inorganic hybrid perovskites (OIHPs) have drawn tremendous attention on account of their structural tunability, simple synthesis methods, and superior properties. Among these, 2D cadmium-based perovskites, exhibiting reversible phase transition, photoluminescence, and ferroelectric properties, have been reported. Herein, we have synthesized a new Ruddlesden–Popper (RP) type perovskite, (thiophene-2-methylammonium)2CdCl4, which possesses blue-white emission and high phase-transition temperature. Thus, the compound might have potential applications in temperature sensor, dielectric switch or light-emitting diode (LED) fields. In brief, this study presents a valuable perspective on the design and synthesis of 2D cadmium-based multifunctional perovskites. [ABSTRACT FROM AUTHOR]

2D hybrid halide double perovskites (HHDPs) have been demonstrated to be a promising alternative to conventional lead‐based halide perovskites as a new system of photoferroelectrics, due to their unique characteristics of environmental friendliness, favorable stability, and fascinating optoelectronic properties. Herein, for the first time, a 2D iodide double perovskite photoferroelectric is reported based on Ag/Sb ions, (4,4‐DFPD)4AgSbI8 (4,4‐DFPD = 4,4‐difluoropiperidinium), which possesses a high Curie temperature of 414 K (above BaTiO3), a large spontaneous polarization of 9.6 μC cm−2, ferroelectric photovoltaic effect, and photostrictive effect. Notably, to the best of the authors' knowledge, the discovery of photostriction in HHDP photoferroelectrics is unprecedented. Moreover, (4,4‐DFPD)4AgSbI8 exhibits an impressive X‐ray responsivity, with a sensitivity as high as 704.8 μC Gyair−1 cm−2 at 100 V bias and a detection limit as low as 0.36 μGyair s−1 at 10 V bias, both of which outperform the current all HHDP photoferroelectrics. This work enriches the photoferroelectric family, and proves that Ag/Sb‐based HHDP photoferroelectrics are a promising candidate for the next‐generation optoelectronic devices. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: The broad operating temperature range is sought for molecular ferroic materials who are expected to be applied to flexible and electronic materials. Hydrogen bonds, an effective force between molecules, are important to regulate the molecule structure and their condition, helping a higher temperature range for ferroic materials. Here, we report a molecular perovskite ferroelastic (Me‐Hdabco)Rb[BF4]3 (Me‐Hdabco = N‐methyldabconium) which shows high temperature (T1 = 322.5 K and T2 = 381 K) ferroelastic phase transitions. The ferroelastic phase transition temperature range of (Me‐Hdabco)Rb[BF4]3 is significantly increased by 71 K compared with [Meda‐bco‐F]Rb[BF4]3 (Medabco‐F = 1‐fluoro‐4‐methyl‐1,4‐diazoniabicyclo[2.2.2]octane). Structural analysis and thermal analysis demonstrate the ferroelastic phase transition is mainly attributed to dynamic cations order and disorder transformation. Therefore, new hydrogen bonds generated between cations and the Rb8[BF4]12 frame increase their intermolecular force, which is beneficial to improving the phase transition temperature. This finding has an important impact on the utilization of weak interaction forces to design and optimize functional materials. [ABSTRACT FROM AUTHOR]

As a feasible lead-free scheme, organic–inorganic hybrid double perovskites show many excellent properties, including ferroelectricity, ferroelasticity, self-powered circularly polarized light detection and so on. In this work, the solid-to-solid structural phase transition of a two-dimensional hybrid double perovskite (CHA)4CuBiI8 was successfully activated via the dehydration of (CHA)4CuBiI8·H2O, which was proven by differential scanning calorimetry (DSC) and temperature-dependent dielectric measurements. Using variable-temperature single-crystal X-ray diffractometry, the cause behind the phase transition of (CHA)4CuBiI8 was determined to be the overall coordination of distortion and movement of the inorganic skeleton and thermal deformation of the cationic structure. In addition, the substance after dehydration shows good stability in multiple reversible switching during dielectric tests. The interesting dehydration-activated results of the material contribute towards a further expansion of the properties and potential application of hybrid double perovskites. [ABSTRACT FROM AUTHOR]

Organic–inorganic hybrid ABX3 perovskite (OIHPs) with phase transition have considerable application potential in multifunctional devices for their structural tunability and excellent photo/electric performance. Because the interaction between molecules during the crystallization process is difficult to predict and control, exploring targeted chemical design methods to synthesize phase change materials has been an interesting and challenging problem. As per the synergistic effect of anion and cation, we assemble a cation with high vibrational activity and an inorganic anion with large voids to successfully design a one-dimensional OIHPs phase change material. [FMPD][Cd(SCN)3] (FMPD = 1-fluoroethyl-1-methylpiperidinium) undergoes two reversible phase transitions above room temperature with the substitution of methyl with fluoroethyl increasing the energy barrier of molecular motion. The individual crystal diffraction structures show that, unlike the phase change caused by the reorientation of organic cations in majority of known perovskites, this phase transition is triggered by the order/disorder of cations and anions related to the vibration increase by the introduction of fluoroethyl. The results provide a new design idea for the design and assembly of novel OIHPs-type phase change materials. [ABSTRACT FROM AUTHOR]

Organic–inorganic hybrid perovskite‐type multiferroics have attracted considerable research interest owing to their fundamental scientific significance and promising technological applications in sensors and multiple‐state memories. The recent achievements with divalent metal dicyanamide compounds revealed such malleable frameworks as a unique platform for developing novel functional materials. Herein, two 3D organic–inorganic hybrid perovskites [Et3P(CH2)2F][Mn(dca)3] (1) and [Et3P(CH2)2Cl][Mn(dca)3] (2) (dca=dicyanamide, N(CN)2−) are presented. Accompanying the sequential phase transitions, they display a broad range of intriguing physical properties, including above room temperature ferroelastic behavior, switchable dielectricity, and low‐temperature antiferromagnetic ordering (Tc=2.4 K for both 1 and 2). It is also worth noting that the spontaneous strain value of 1 is far beyond that of 2 in the first ferroelastic phase, as a result of the precise halogen substitution. From the point view of molecular design, this work should inspire further exploration of multifunctional molecular materials with desirable properties. [ABSTRACT FROM AUTHOR]

Both 3D organic–inorganic perovskites ([Et3P(CH2)2Cl][Cd(dca)3] (1) and [Et3P(CH2)2F][Cd(dca)3] (2) [dca = dicyanamide, N(CN)2−]) display two sequentially reversible high-temperature phase transitions and switchable dielectric properties. Through halogen substitution, 1 shows exceptional switching behaviour of second harmonic generation effects and remarkably 2 represents the first above-room-temperature 3D ferroelastic material characterized by two ferroelastic phases. [ABSTRACT FROM AUTHOR]

Molecular bistable dielectric switches represent a class of highly desirable intelligent materials due to their sensitive switchable responses, simple and environmentally friendly processing, light weights, and mechanical flexibility. However, most of these switches can only work at a very low temperature, extremely limiting their potential applications. Herein, three layered organic–inorganic hybrid perovskite-type compounds of the general formula A2BX4, [NH3(CH2)2Cl]2[CdCl3Br] (1), [NH3(CH2)2Cl]2[CdCl4] (2) and [NH3(CH2)2Cl]2[CdBr4] (3), which display sensitive dielectric switching reversibility and remarkable switching anti-fatigue, have been successfully designed. Differential scanning calorimetry and dielectric measurements for 1 confirm its reversible phase transition at around 166 K. Through anion modulation, the phase transition temperatures of 2 and 3 can be greatly improved up to 237 K and 254 K, respectively. Structural analysis discloses that the phase transition temperature's shifts may result from the differences among the inorganic frameworks. Moreover, due to the significant order–disorder transitions of ammonium cations, the permittivities of 1, 2 and 3 change abruptly at around the phase transition points, making them excellent stimuli-responsive electrical switches. Such an anion-modulated method will open up new possibilities of highly efficiently tuning the phase transition temperature of molecular bistable dielectric switches. [ABSTRACT FROM AUTHOR]

A bistable optical–electrical duple switch belongs to a class of highly satisfying intelligent materials that can transform optical and electrical responses simultaneously in one device. A perovskite-type high-temperature phase transition compound with one-dimensional chain-like crystal structure, ([(CH3)3PCH2OCH3][PbBr3], 1), displays remarkable bistable photoluminescent-dielectric duple switching behaviors. The noteworthy order–disorder transition of the phosphonium cation and the motions of anions contribute to the phase transition, leading to the space group P21/c at a low temperature phase to C2/c at a high temperature phase. 1 exhibits a prominent step-like dielectric anomaly at 401.0 K and demonstrates novel optical properties with a band gap of 3.54 eV. The photoluminescence intensity suddenly declines from 398 K to 408 K, which may be attributed to the occurrence of phase transition. The electron cloud distributions of the frontier orbital in compound 1 have been calculated using a DFT program. [ABSTRACT FROM AUTHOR]

A new organic–inorganic perovskite-type compound [(CH3)3PCH2OH][CdBr3] exhibits a ferroelastic phase transition at 339 K. Domain structures were observed and analyzed. The origin of the phase transition can be attributed to the motion or reorientation of the [(CH3)3PCH2OH]+ cations and the displacement of Cd2+ and Br− ions in solid-state crystals. [ABSTRACT FROM AUTHOR]

Keywords: dimensions; ferroelasticity; ferroelastic domains; perovskites; phase transitions EN dimensions ferroelasticity ferroelastic domains perovskites phase transitions 1 1 1 10/28/22 20221021 NES 221021 Organic-inorganic hybrid perovskite ferroelastics have received particular attention by taking advantages of their low-cost, light-weight, easy preparation, and mechanical flexibility. Dimensions, ferroelasticity, ferroelastic domains, perovskites, phase transitions This review article summarizes the structural design strategies of organic-inorganic hybrid perovskite ferroelastic materials, as well as the opportunities and challenges in the future. [Extracted from the article]

Hybrid organo-metal halide perovskite materials, such as CH3NH3PbI3, have been shown to be some of the most competitive candidates for absorber materials in photovoltaic (PV) applications. However, their potential has not been completely developed, because a photovoltaic effect with an anomalously large voltage can be achieved only in a ferroelectric phase, while these materials are probably ferroelectric only at temperatures below 180 K. A new hexagonal stacking perovskite-type complex (3-pyrrolinium)(CdCl3) exhibits above-room-temperature ferroelectricity with a Curie temperature Tc=316 K and a spontaneous polarization Ps=5.1 μC cm−2. The material also exhibits antiparallel 180° domains which are related to the anomalous photovoltaic effect. The open-circuit photovoltage for a 1 mm-thick bulky crystal reaches 32 V. This finding could provide a new approach to develop solar cells based on organo-metal halide perovskites in photovoltaic research. [ABSTRACT FROM AUTHOR]

Hybrid organo-metal halide perovskite materials, such as CH3NH3PbI3, have been shown to be some of the most competitive candidates for absorber materials in photovoltaic (PV) applications. However, their potential has not been completely developed, because a photovoltaic effect with an anomalously large voltage can be achieved only in a ferroelectric phase, while these materials are probably ferroelectric only at temperatures below 180 K. A new hexagonal stacking perovskite-type complex (3-pyrrolinium)(CdCl3) exhibits above-room-temperature ferroelectricity with a Curie temperature Tc=316 K and a spontaneous polarization Ps=5.1 μC cm−2. The material also exhibits antiparallel 180° domains which are related to the anomalous photovoltaic effect. The open-circuit photovoltage for a 1 mm-thick bulky crystal reaches 32 V. This finding could provide a new approach to develop solar cells based on organo-metal halide perovskites in photovoltaic research. [ABSTRACT FROM AUTHOR]

Molecular ferroelectric thin films are highly desirable for their easy and environmentally friendly processing, light weight, and mechanical flexibility. A thin film of imidazolium perchlorate processed from aqueous solution is an excellent molecular ferroelectric with high spontaneous polarization, high Curie temperature, low coercivity, and superior electromechanical coupling. These attributes make it a molecular alternative to perovskite ferroelectric films in sensing, actuation, data storage, electro-optics, and molecular/flexible electronics. [ABSTRACT FROM AUTHOR]

Three‐dimensional (3D) pseudohalide rare‐earth double perovskites (PREDPs) have garnered significant attention for their versatile physical properties, including ferroelectricity, ferroelasticity, large piezoelectric responses, and circularly polarized luminescence. However, their potential for X‐ray detection remains unexplored, and the low Curie temperature (TC) limits the performance window for PREDP ferroelectrics. Here, by applying the chemical regulation strategies involving halogen substitution on the organic cation and Rb/Cs substitution to the PREDP [(R)‐M3HQ]2RbEu(NO3)6 [(R)‐M3HQ=(R)‐N‐methyl‐3‐hydroxylquinuclidinium] with a low TC of 285 K, a novel 3D PREDP ferroelectric [(R)‐CM3HQ]2CsEu(NO3)6 [(R)‐CM3HQ=(R)‐N‐chloromethyl‐3‐hydroxylquinuclidinium] are successfully synthesized, for which the TC reaches 344 K. More importantly, such a strategy endowed [(R)‐CM3HQ]2CsEu(NO3)6 with notable X‐ray detection capabilities. Centimeter‐sized [(R)‐CM3HQ]2CsEu(NO3)6 single crystals fabricated from aqueous solutions demonstrated a sensitivity of 1307 μC Gyair−1 cm−2 and a low detectable dose rate of 152 nGyair s−1, the highest sensitivity reported for hybrid double perovskite ferroelectric detectors. This work positions PREDPs as promising candidates for the next generation of eco‐friendly optoelectronic materials and also offers substantial insights into the interaction between structure, composition, and functionality in ferroelectric materials. [ABSTRACT FROM AUTHOR]

A 3D pseudohalide rare- earth double perovskite ( PREDP) exhibiting high- temperature ferroelectricityand excellent X- ray response sensitivity has been developed. The synthesis of PREDPS only requires an aqueous solution and boasts high stability. According to the findings of Chuang Ma, Da- Wei Fu, Yi Zhang et al. ( e202413726), PREDPs hold great promise as potential candidates for the next generation of environmentally friendly optoelectronic materials. [Extracted from the article]

Hybrid organo-metal halide perovskite materials, such as CH3NH3PbI3, have been shown to be some of the most competitive candidates for absorber materials in photovoltaic (PV) applications. However, their potential has not been completely developed, because a photovoltaic effect with an anomalously large voltage can be achieved only in a ferroelectric phase, while these materials are probably ferroelectric only at temperatures below 180 K. A new hexagonal stacking perovskite-type complex (3-pyrrolinium)(CdCl3) exhibits above-room-temperature ferroelectricity with a Curie temperature Tc=316 K and a spontaneous polarization Ps=5.1 μC cm−2. The material also exhibits antiparallel 180° domains which are related to the anomalous photovoltaic effect. The open-circuit photovoltage for a 1 mm-thick bulky crystal reaches 32 V. This finding could provide a new approach to develop solar cells based on organo-metal halide perovskites in photovoltaic research. [ABSTRACT FROM AUTHOR]

Hybrid organo-metal halide perovskite materials, such as CH3NH3PbI3, have been shown to be some of the most competitive candidates for absorber materials in photovoltaic (PV) applications. However, their potential has not been completely developed, because a photovoltaic effect with an anomalously large voltage can be achieved only in a ferroelectric phase, while these materials are probably ferroelectric only at temperatures below 180 K. A new hexagonal stacking perovskite-type complex (3-pyrrolinium)(CdCl3) exhibits above-room-temperature ferroelectricity with a Curie temperature Tc=316 K and a spontaneous polarization Ps=5.1 μC cm−2. The material also exhibits antiparallel 180° domains which are related to the anomalous photovoltaic effect. The open-circuit photovoltage for a 1 mm-thick bulky crystal reaches 32 V. This finding could provide a new approach to develop solar cells based on organo-metal halide perovskites in photovoltaic research. [ABSTRACT FROM AUTHOR]

Organic–inorganic hybrid perovskite‐type multiferroics have attracted considerable research interest owing to their fundamental scientific significance and promising technological applications in sensors and multiple‐state memories. The recent achievements with divalent metal dicyanamide compounds revealed such malleable frameworks as a unique platform for developing novel functional materials. Herein, two 3D organic–inorganic hybrid perovskites [Et3P(CH2)2F][Mn(dca)3] (1) and [Et3P(CH2)2Cl][Mn(dca)3] (2) (dca=dicyanamide, N(CN)2−) are presented. Accompanying the sequential phase transitions, they display a broad range of intriguing physical properties, including above room temperature ferroelastic behavior, switchable dielectricity, and low‐temperature antiferromagnetic ordering (Tc=2.4 K for both 1 and 2). It is also worth noting that the spontaneous strain value of 1 is far beyond that of 2 in the first ferroelastic phase, as a result of the precise halogen substitution. From the point view of molecular design, this work should inspire further exploration of multifunctional molecular materials with desirable properties. [ABSTRACT FROM AUTHOR]

A bistable optical–electrical duple switch belongs to a class of highly satisfying intelligent materials that can transform optical and electrical responses simultaneously in one device. A perovskite-type high-temperature phase transition compound with one-dimensional chain-like crystal structure, ([(CH3)3PCH2OCH3][PbBr3], 1), displays remarkable bistable photoluminescent-dielectric duple switching behaviors. The noteworthy order–disorder transition of the phosphonium cation and the motions of anions contribute to the phase transition, leading to the space group P21/c at a low temperature phase to C2/c at a high temperature phase. 1 exhibits a prominent step-like dielectric anomaly at 401.0 K and demonstrates novel optical properties with a band gap of 3.54 eV. The photoluminescence intensity suddenly declines from 398 K to 408 K, which may be attributed to the occurrence of phase transition. The electron cloud distributions of the frontier orbital in compound 1 have been calculated using a DFT program. [ABSTRACT FROM AUTHOR]

Molecular piezoelectrics are highly desirable for their easy and environment-friendly processing, light weight, low processing temperature, and mechanical flexibility. However, although 136 years have passed since the discovery in 1880 of the piezoelectric effect, molecular piezoelectrics with a piezoelectric coefficient d33 comparable with piezoceramics such as barium titanate (BTO; ~190 picocoulombs per newton) have not been found. We show that trimethylchloromethyl ammonium trichloromanganese(II), an organic-inorganic perovskite ferroelectric crystal processed from aqueous solution, has a large d33 of 185 picocoulombs per newton and a high phase-transition temperature of 406 kelvin (K) (16 K above that of BTO). This makes it a competitive candidate for medical, micromechanical, and biomechanical applications. [ABSTRACT FROM AUTHOR]

• The Pb-based perovskite exhibits a red-light photoluminescence. • The dual phase changes of photoluminescence and dielectric were shown. • The step-like dielectric switching was observed at higher temperature. Intelligent multifunctional materials are indispensable for the electronic devices, but the existing applied counterparts have the disadvantage that their structures cannot be adjusted to meet diversified application requirements. Therefore, organic-inorganic hybrid perovskites with the inherent advantage of structural diversity are expected to become promising intelligent multifunctional materials. Based on the diversity of perovskites mentioned above, we have reported a series of dielectric switches. Here, a new one-dimensional organic-inorganic hybrid perovskite (N-fluoroethyl-N-methylmorpholine)PbBr 3 was reported. In this distorted octahedral perovskite, a step-like dielectric switching was observed at around 343 K upon heating and 325 K upon cooling. Simultaneously, photoluminescence is also related to the highly distorted octahedron, and this one-dimensional Pb-based halide exhibits a red-light with CIE chromaticity coordinates of (0.56, 0.42) upon ultraviolet photoexcitation. In short, the reversible/switchable dielectric phase transition and photoluminescence characteristic in this hybrid perovskite was successfully achieved, which are expected to be applied in optoelectronic devices and dielectric switches, and promote the development of organic-inorganic hybrid multifunctional materials. [Display omitted] [ABSTRACT FROM AUTHOR]