Recent Advances on the Applications of Luminescent Pb2+-Containing Metal–Organic Frameworks in White-Light Emission and Sensing

Luminescent Pb²⁺-based metal–organic frameworks (MOFs) belong to a new class of multifunctional molecular materials with interesting luminescence properties and potential applications within a single crystalline phase. In this mini review, we present the recent advances that have been achieved in their applications as single-phase white-light emitting materials and chemosensors in the last decade. We focus on the trends in the modification of their structures and luminescence by various bridging ligands, and subsequently their multifunctional applications, which may affect the future development of the field.

Introduction

Metal–organic frameworks (MOFs), a class of coordination crystalline materials involving metal nodes and multi-topic ligands, have attracted broad interest, as a result of their novel structures and various applications (Wang and Astruc, 2019). Until recent years, most of the reported MOFs were constructed on the basis of d-block and f-block metals (Cui et al., 2012; Zhou et al., 2015). In contrast, much less is understood on main-group MOFs, especially Pb²⁺-containing MOFs, mainly as a result of their flexible geometry and nonclassical coordination chemistry. As with other heavier metals, the toxicity of Pb²⁺, a heavy p-block element, has drawn certain environmental concerns. However, the interesting emission properties of Pb²⁺-based materials, which are highly dependent on the coordination environment, and thus their potential for different applications, have also attracted much interest. The optical and electronic properties of Pb²⁺ compounds have recently been explored in various applications, such as Pb²⁺-based perovskite (Nazarenko et al., 2018), white-light emitting material (Peng et al., 2018), X-ray scintillator (Lu et al., 2019), luminescent sensing (Wang et al., 2018), batteries (Hu et al., 2017), nonlinear optical materials (Chen et al., 2020), ferroelectric materials (Gao et al., 2017), and semiconductors (Terpstra et al., 1997). These fascinating properties are closely associated with its heavy atom effect, inert lone pair effect, large ionic radius, and its borderline position on the hard–soft acid–base scale (Chu et al., 2013). Pb²⁺-based MOFs exhibit frequently unique luminescent properties and applications which are seldom realized in other metal-based MOFs, and thus represent an interesting class of functional materials for the study of structure–property correlations. Since the luminescence properties of Pb²⁺-based MOFs are highly important to their functionality, especially in the application as fluorescent sensors, a brief introduction to the nature of their emission properties will be provided initially, which is followed by the discussion on their applications as white-light emitting materials and luminescent sensors.

Luminescent Properties of Pb²⁺-Based MOFs

Luminescent metal complexes of Ln³⁺, Zn²⁺, Cd²⁺, and Cu⁺, and noble metals (Ru²⁺, Os^2+/6+, Ir³⁺, Pt²⁺, and Re^+/5+) have been well documented, and their emission properties are usually predictable (Cui et al., 2012; Zhou et al., 2015). In contrast, the luminescence properties of Pb²⁺ compounds are more complicated, as they may exhibit simultaneously a variety of electronic transitions, including (1) the metal-centered (MC) s→p transition that usually occurs in hemi-directed Pb²⁺ compounds (Pan et al., 2018), (2) ligand-to-metal charge transfer (LMCT) (Pan et al., 2018), (3) Pb²⁺-perturbed ligand-centered π→π* transition (Pan et al., 2018), and (4) metal-to-ligand charge transfer (MLCT) (Chu et al., 2013). The emissions of Pb²⁺ compounds are usually phosphorescence, irrespective of their emission natures, as spin–orbital coupling is enhanced by the heavy atom effect of Pb²⁺. In addition, the luminescence of Pb²⁺-based MOFs is sensitive to the substituents on the ligands and the subtle changes in their macrostructures. Thus, interesting luminescence properties were often reported for Pb²⁺-based MOFs. For example, a novel 3D Pb²⁺ MOF Pb₄(L¹)₃(μ⁴-O)(H₂O) (1) (H₂L¹ = 1,3-benzenedicarboxylate) exhibiting an eight-connected bcu-type topological motif has been synthesized by Yang et al. (2008). Upon excitation at 374 nm, the Pb²⁺ MOF shows an emission at 424 nm, which is assigned to LMCT from delocalized π bonds of carboxylate groups to p orbitals of Pb²⁺ ion. In contrast, Pb²⁺-based MOFs with MLCT character are rare, as the Pb(III) state is not readily accessible. However, Sun and coworkers have recently reported two lead(II) carboxyphosphonate compounds [Pb₂Cl₃(H₂L²)]·H₂O (2) and [Pb₂(HL²)(HL³)] (3) (H₃L² = 1-(phosphonomethyl)piperidine-4-carboxylic acid and H₃L³ = 1,3,5-benzenetricarboxylic acid), which show a significant red shift and enhancement of the emission compared with the free H₃L³ ligand, probably attributed to the MLCT transition (Chu et al., 2013). Moreover, owing to the presence of stereochemically active lone pair effect, the emissions from the metal-centered (MC) s→p transition are most commonly found in semidirectionally coordinated Pb²⁺-MOFs.

Pb²⁺-Based MOFs as Single-Phase White-Light Emitting Materials

In this part, the recent development in Pb²⁺-based organic–inorganic hybrid materials with white-light emission (WLE) and their photophysical properties will be discussed in relation with the structures of the ligands and the MOFs. Materials with WLE have attracted immense interests as a consequence of their potential usage in displays and lightings. Currently, most of the white-light sources are fabricated by a combination of emissions from separate dopants or a blending of multiple components. However, these materials may bring along complications and higher cost in the fabrication process, together with intrinsic problems such as reabsorption, phase separation, and color variation. The construction of single-phase WLE materials is therefore considered an ideal approach to overcome these issues. To achieve high-quality white light, the single-phase materials must exhibit emission with the Commission Internationale de l’Eclairage (CIE) coordinates (0.33, 0.33). Pb²⁺-based MOFs are found to be potential single-phase materials for WLE, since the multiple emitting centers necessary for WLE could be achieved by suitable combination of organic moieties and Pb²⁺, which exhibits emissions of different origins.

Hybrid organic–inorganic lead halide perovskites were reported to be a special class of intrinsic broadband white-light emitters. The incorporation of structurally deformable Pb_mX_n units into MOFs was a convenient method for the crystal engineering of optoelectric materials. In some cases, the emission solely originates from the lead halide units, and the ligands function only as bridging groups to stabilize the MOFs, whereas the introduction of π-conjugated aromatic moiety was suggested to significantly influence the emission properties by their readily accessible and modifiable charge-transfer bands. Several examples of Pb²⁺ halide perovskites bearing aliphatic dicarboxylate linkage groups were reported. For example, two 2D Pb²⁺ halide polymeric complexes [Pb₂X₂][L⁴] (X = Cl, 4 and Br, 5) with broadband WLE were obtained from the reactions of PbX₂ and trans-1,4-cyclohexanedicarboxylic acid (H₂L⁴) under hydrothermal conditions. These materials were chemically robust over a wide pH range (3–9) and exhibited undiminished luminescence upon UV excitation for 30 days. The WLE was suggested, by DFT calculations, to originate from the Pb–Pb dimerization and Cl–Cl pairing in the [Pb₂X₂]²⁺ (X = Cl/Br) layers (Supplementary Table S1) (Yin J. et al., 2019). Two cationic porous 3D organic–metal halide frameworks [Pb₂Br₂][L⁵] (6) and [Pb₃Br₄][L⁶] (7) were prepared from bromoplumbate and aliphatic dicarboxylate bridging ligands. These compounds exhibit high chemical resistance and intrinsic white-light emission (λ_ex = 360 nm) at high quantum efficiency. The WLE spanned the whole visible-light spectrum and was suggested to arise from the electron–phonon coupling in the strongly deformable and anharmonic lattice (Peng et al., 2018). A series of cationic layered lead halide materials, formulated as [Pb₂X₂]²⁺[L⁵] (X = F, Cl and Br) (8–10), were later reported by the same group to exhibit intense broadband WLE in the bulk form at an external quantum efficiency up to 11.8% (Zhuang et al., 2017).

Aromatic dicarboxylate bridging ligands in lead halide perovskites were found to influence the photophysical properties significantly. Several Pb²⁺ MOFs have been prepared by using derivatized aromatic dicarboxylate bridging moieties, and the study of the dependence of their photophysical properties on the aromatic ring may provide more insights for the development of single-phase WLE materials. These compounds usually exhibit dual or multi-emission bands, in contrast to conventional luminescent materials. Owing to the lone pair effect, the emissions from the MC s→p transition are readily found in Pb²⁺ MOFs with a semi-directional geometry. On the other hand, suitable bridging ligands are crucial in making the ligand-centered and charge-transfer (LMCT/MLCT) transitions accessible in these Pb²⁺ MOFs. Three stable WLE-MOFs, [Pb₂X₃⁺][L⁷]₂ [(CH₃)₂NH₂⁺]₃ (X = Cl/Br/I) (11–13), were afforded by bridging the deformable [Pb₂X₃]⁺ (X = Cl, Br, and I) 1D chains with 1,4-benzenedicarboxylate (H₂L⁷) (Supplementary Figure S1). Upon near-UV excitation, these materials exhibit intrinsic broadband emissions with a high color-rendering index (CRI) of up to 89 (Peng et al., 2019). Whereas their emissions of 11–13 are mainly originated from the [Pb₂X₃⁺] moieties, the introduction of dicarboxylate linkers with rigid aromatic moiety was found to significantly enhance the contribution from the ligand-centered emission and was an effective means for tuning the luminescent properties of the MOFs. For example, single-component broadband photoemitters, [(Pb₄X₂)(L⁸)₄·A₂]_n (X = Cl 14, Br 15, and I 16, A = (CH₃)₃NH⁺ and (CH₃)₂NH₂⁺), were formed by bridging 1D haloplumbate chains with the rigid luminescent 2,6-naphthalene dicarboxylate (H₂L⁸). The bromo and iodo analogs exhibited WLE, which were attributed to the ligand-centered blue emissions from the extended conjugation in L⁸ and the red emissions from the hemi-directed haloplumbate centers (Lin et al., 2020). Xu and coworkers synthesized two emissive 3D networks, PbL⁹ (17) and PbL¹⁰ (18), with 1,4-benzenedicarboxylic acid modified, respectively, with CH₃SCH₂CH₂S- (L⁹) and (S)-H₃(OH)CHCH₂S- (L¹⁰) at the 2 and 5 positions (Figure 1). The two compounds featured, respectively, a yellowish-green photoluminescence (17) and a bright WLE (18) resulting similarly from broadband dual emissions of different origins. The white emission of 18 was attributed to a suitable ratio of LMCT and s→p transitions, while in 17, the contribution from LMCT was more significant. A thin film of 18 was then applied onto a commercially available UV-LED lamp by a dip-coating procedure (Figure 1) and demonstrated to work in conventional lighting application (He et al., 2012). Wibowo and coworkers have recently synthesized two Pb²⁺-based MOFs, Pb(HL³)(1,4-dioxane)0.5 (19) and Pb₂(HL³)₂(H₂O)₅ (20), by using a dissolution–crystallization method (H₃L³ = benzene-1,3,5-tricarboxylic acid). These complexes contained similar linear subunits that were interconnected by HL³ into three-dimensional porous MOFs. The two compounds exhibit broad emissions, probably originating from a mixture of ILCT, LMCT, and/or MLCT, upon excitation at λ_ex = 350 nm. Particularly, the CIE coordinates (0.33, 0.36) of 20 are close to the ideal CIE coordinates (0.33, 0.33) for WLE (Al-Nubi et al., 2019).

FIGURE 1

FIGURE 1. (A) Local coordination environment around the Pb²⁺ ion and white LED based on complex [Pb(L¹⁰)]. (B) CIE coordinates for emissions of [Pb(L⁹)] (λ_ex = 365 nm) and [Pb(L¹⁰)].

In addition to carboxylate moieties, N-heterocycles have also emerged as important linkage groups in Pb²⁺ MOFs. Zeng and coworkers have recently reported three Pb²⁺ MOFs, [Pb₂(L¹¹)₂(DMA)]·DMA (21), [Pb₂(L¹¹)₂(DMF)]·1.5DMF (22), and [Pb₂(L¹¹)₂(DMF)]·NEt₃ (23) (H₂L¹¹ = 5-(pyridin-4-yl)isophthalic acid, DMA = N,N-dimethylacetamide) (Supplementary Figure S3). These bulk MOF materials had iso-reticular structures with 1D square or rhombic channels with subtle difference in Pb²⁺ coordination geometry. Optical experiments showed that 21 was an excellent white emitter with multiple advantages, including pure white color with the chromaticity coordinates (0.331, 0.347) (λ_ex = 350 nm), high fluorescence intensity, and good compatibility to human visibility (Yin Z. et al., 2019). Hydrothermal reaction of pyridine-2,6-dicarboxylic acid (H₂L¹²) and Pb(NO₃)₂ afforded a rhombic-like 2D polymer [Pb(L¹²)] (24) (Qi et al., 2018). Upon excitation at λ_ex = 340 nm, 24 exhibits a high-energy emission at 441 nm along with two broad low-energy bands at ca. 553 and 662 nm with a high quantum efficiency of 52%. The emission is possibly assigned to a mixture of LMCT and s→p transition of the Pb²⁺ center. The high quantum yield and thermal stability, as well as CIE coordinate (0.28, 0.25), suggested the compound as a potential candidate for solid-state white luminescent materials. Reaction of the structurally related ligand, pyridine-2,5-dicarboxylate ligand (H₂L¹³), with Pb(NO₃)₂ afforded a 3D [Pb(L¹³)(H₂O)] (25) (Wibowo et al., 2010), which is formed by connecting the 1D chains of corner-shared distorted capped trigonal prisms with L¹³. 25 is also a single-phase WLE phosphor covering a wide spectral range; however, its luminescence origin remains unclear. Examples of WLE Pb²⁺ MOFs constructed from bridging ligands containing only N-heterocyclic donor moieties are relatively rare but are important for illustrating the influence of aromatic ligands with extended π-conjugation on their emission, because of the more efficient ligand-centered and LMCT transitions. For example, two Pb²⁺-based coordination polymers, [Pb(NO₃)(L¹⁴)]_n (26) and [Pb(L¹⁴)₂]_n (27), were synthesized from the reactions of 1-tetrazole-4-imidazole-benzene (HL¹⁴) and Pb²⁺ salt in different solvents (Chen et al., 2015). Both compounds exhibit dual emission resulting from different emission origins of LMCT and IL π-π* charge transfer. However, their photoluminescence is dependent on the excitation wavelengths. Recently, Peedikakkal and coworkers reported two Pb²⁺ MOFs, [Pb₂(L¹⁵)(O₂CCH₃)₂(O₂CCH₃)₂]·H₂O (28) and [Pb(L¹⁵)(O₂CCF₃)₂]·1/2CHCl₃ (29), as well as the mononuclear complex [Pb(L¹⁵-H)₂(O₂CCF₃)₄] (30) prepared from the neutral 4,4’-bipyridine (L¹⁵) (Peedikakkal et al., 2018). The solid-state photoluminescence of 28–30 was investigated at room temperature. Upon photoexcitation (λ_ex = 329, 376, and 330 nm, respectively), the compounds showed near-white light emissions with CIE coordinates (0.24, 0.32) for 28, (0.33, 0.39) for 29, and (0.26, 0.31) for 30, which were attributed to mixed LMCT and MC transitions.

Pb²⁺-Based MOFs as Sensors of Ions and Organic Substrates

MOFs have been regarded as one of the promising candidates of fluorescent probes, as a result of the high sensitivity, short response time, portability, and ease of visualization (Kreno et al., 2012). Recent works on Pb²⁺-based MOFs showed that they exhibited the potential to serve as efficient sensor materials, since their luminescence intensity is found to change linearly with the concentration of the analytes, which are absorbed into the MOF structures. Among the Pb²⁺-based MOFs reported so far, multi-responsive luminescent MOFs which could probe more than one analyte were of particular interest.

As in the abovementioned WLE materials, carboxylates were often adopted as bridging ligands in luminescent Pb²⁺-based MOF sensors of ionic and organic analytes. Typical examples are the Pb²⁺-based MOFs containing pyridine-carboxylates. The addition of various functional groups, such as halides and non-coordinated heteroatoms (N or O) on the pyridyl moiety, were found to significantly alter the functions of Pb²⁺-based MOFs, by varying the interaction with the analytes. Recently, Guo and coworkers synthesized two Pb²⁺ complexes, [Pb(L¹⁶)₂]_n (31) and [Pb(L¹⁷)₂]_n (32) (HL¹⁶ = 5-chloronicotinic acid, and HL¹⁷ = 5-bromonicotinic acid), to investigate effect of the halo-substituents on the sensing properties. It was revealed that the chloro-containing 31 acted as a multi-response luminescent sensor toward Cr₂O₇^2‒, Fe³⁺, and TNP in DMF solution (Supplementary Table S2) (Guo et al., 2019; Miao, 2019). Upon substituting the halide groups by -NH₂ and -OH groups, two 3D MOFs, {[Pb₃(L¹⁸)₂Cl₅]·(H₂O)}n (33) and [Pb₂(L¹⁹)Cl₂]_n (34) (HL¹⁸ = 5-aminonicotinic acid; H₂L¹⁹ = 5-hydroxynicotinic acid), have been synthesized, and their functions as luminescent sensors have been compared. Although the non-coordinated donor groups were expected to strengthen the interactions between the MOFs and analytes, very different activities were observed in the two MOFs. 33 was found to be a heterogeneous catalyst for Knoevenagel condensation reaction and exhibited no sensing properties, while 34 was found to be a luminescence sensor for Fe³⁺ with good recyclability (Zhang et al., 2019). Recently, a 2D framework [PbL¹⁸(NO₃)]_n (35), obtained from hydrothermal reaction of HL¹⁸ of Pb(NO₃)₂, acted not only as a luminescent sensor for picric acid but also as a temperature sensor (Wang, 2019). More recently, Gai reported a novel Pb²⁺-containing polymer, [Pb(L²⁰)]·0.5H₂O·0.5CH₃OH (36), containing a zwitterionic ligand 4-carboxy-1-(3,4-dicarboxy-benzyl)-pyridinium chloride (H₃L²⁰Cl) (Supplementary Figure S2). Optical experiments indicated that 36 was a versatile turn-off luminescent sensor, which was multi-responsive toward Cr₂O₇²⁻, CrO₄²⁻, Fe³⁺, and nitrobenzene with a fast response and a high selectivity (Zhao et al., 2020).

As extended π-conjugation in the bridging ligands was suggested to significantly influence the luminescence in Pb²⁺-based MOF, related complexes containing phthalate and its derivatives were also studied for their sensing properties. A pair of enantiomorphic luminescent MOFs, [Pb₁₀(L²¹)₇(NO₃)₆(H₂O)₂] (37) (1P and 1M) (H₂L²¹ = 5-methylisophthalic acid), which possess a novel {Pb¹⁸} wheel and a chiral 3D inorganic connectivity, were reported to act as a rapid and highly selective sensor toward Co₂⁺ (Han et al., 2014). Modification of the MOF polymeric structures and their sensing properties was also explored by the co-reaction with bridging ligands of other acidic moieties. Dong and coworkers have prepared two luminescent Pb²⁺-phosphonate MOFs, the 2D [Pb₃(L²²)₂(HL²³)(H₂O)₂] (38) and 3D [Pb₂(L²⁴)0.5 (L²⁵)(H₂O)₂]·H₂O (39) frameworks, which bore both aromatic carboxylates (H₃L²³ = 5-sulfosalicylic acid, and NaH₂L²⁵ = 5-sulfoisophthalic acid sodium) and amino methylenephosphonates (H₂L²² = (morpholinomethyl)phosphonic acid and H₄L²⁴ = (piperazine-1,4-diylbis (methylene))bis (phosphonic acid)) as the bridging ligands, under hydrothermal conditions. The compounds were demonstrated to be highly selective fluorescent probes for sensing thymine and VO₃⁻, respectively, via fluorescent quenching (Supplementary Figure S4) (Cai et al., 2018). Multi-responsive and multifunctional MOFs were also obtained on introduction of N-heterocycles onto the aromatic linkage moieties. The hydrothermal reactions of the 1,4-bis-(imidazol-1-yl)terephthalic acid (H₂L²⁶) with Pb²⁺ in different solvents afforded a 3D framework with two different isomeric forms, [Pb(L²⁶)]_n (40) ((4,5,6)-c net) and [Pb(L²⁶)]_n (41) (6-c pcu net), which could be used in fluorescent sensing of different ions, that is, Fe³⁺ and Cr₂O₇²⁻ (Wang et al., 2018). A new Pb²⁺-based 2D MOF, {[PbNa(L²⁷)](H₂O)(DMF)₂}_n (42) containing the π-conjugated ligand 4’-(1H-tetrazol-5-yl)-[1,10-biphenyl]-3,5-dicarboxylate (H₃L²⁷), was found to not only act as a luminescent sensor for the detection of nitroaromatic compounds and ferric ions but also show excellent activity for the photodegradation of methylene orange (Wu et al., 2018).

Recently, N-heterocycles, for example, imidazolyl and tetrazolyl, with extended π-conjugation, have been adopted as the building blocks in Pb²⁺-based MOF fluorescent probes. As the multiple donor atoms and the π-conjugation on these ligands are sensitive to environmental changes, the resultant MOF fluorescent probes would contain, in their polymeric structures, uncoordinated N-donor atoms which were suggested to interact with different analytes and instruments in multi-responsive luminescent probes for the simultaneous detection of different analytes. The Pb²⁺-based coordination polymer [Pb(L²⁸)(NO₃)₂]_n (43) (L²⁸ = 1,4-bis(imidazol-1-yl)benzene), which featured a homochiral double stranded helical structure, was reported to be a luminescent sensor for detecting Fe³⁺ ions in aqueous solution with high sensitivity (Sun et al., 2019). A stable 3D MOF [Pb₃O₂L²⁹] (44) was obtained from the hydrothermal reaction of 4-(1H-tetrazol-5-yl)phenol ligand (H₂L²⁹) and Pb²⁺ salt. The compound was a sensitive probe for multi-responsive detection of trace amounts of nitroaromatic compounds and Fe³⁺ in aqueous media, with visible color changes (Luo et al., 2017). A cage-containing chain [Pb₅(L³⁰)₆(N₃)₂(OH)₂]_n (45) and an 1D double helical chain [Pb(L³¹)(N₃)]_n (46) with 1D channels were prepared by solvothermal reactions of the tetrazolyl ligands HL¹⁷ or HL¹⁸ with Pb²⁺ salts (Figure 2) (HL³⁰ = 2-(1H-tetrazol-5-yl)quinoline; HL³¹ = 2-(1H-tetrazol-5-yl)-1,10-phenanthroline) (Xiang et al., 2016). Both MOF structures were reported to uptake different metal ions (Pb²⁺, Hg²⁺, Zn²⁺, and Cd²⁺) and exhibit varied luminescence responses which are transduced as the change in emission wavelengths and are distinguishable with naked eye, rendering them ideal candidates for sensing different heavy metal ions.

FIGURE 2

FIGURE 2. (A) Perspective view and (B) one of the cavities of 1D chain cage structure of [Pb₅(L³⁰)₆(N₃)₂(OH)₂] cluster. (C) Coordination environment of Pb²⁺ ions in two adjacent molecules and (D) 3D porous structure of [Pb(L³¹)(N₃)]_n. The emission spectra of (E) [Pb₅(L³⁰)₆(N₃)₂(OH)₂]_n and (G) [Pb(L₃₁)(N₃)]_n suspended in the aqueous solution and in 0.005 M MCl₂ aqueous solutions (M = Zn²⁺, Cd²⁺, Hg²⁺, and Pb²⁺) with λ_ex = 360 nm. The photographs of aqueous suspensions of (F) [Pb₅(L³⁰)₆(N₃)₂(OH)₂]_n and (H) [Pb(L³¹)(N₃)]_n under normal lighting condition and UV excitation.

Conclusion and Future Outlook

In this review, we have summarized the development of Pb²⁺-based photoluminescent MOFs. Compared with MOFs of block-d and block-f elements, multifunctional Pb²⁺-based MOFs are still a new area of research. These Pb²⁺ MOFs have shown the potentials for the unique applications, especially in single-phase WLE and ion/molecular sensing, owing to the special coordination features associated with their Pb²⁺ centers. At present, most of Pb²⁺-based MOFs are mainly constructed by bridging carboxylic acid ligands. The design and synthesis of novel functional Pb²⁺-based MOFs containing various N-heterocyclic ligands with multiple donor atoms, such as imidazole and tetrazole, are suggested to be an effective alternative to engineer and tailor their properties for a given purpose. Since these moieties have pK_a values similar to those of carboxylic acid, their more versatile coordination modes and extended π-conjugated systems will also have a significant influence on the structures and emission properties of the resultant MOFs. In addition, their multiple donor atoms will also provide additional sites of interaction with substrates/analytes of different properties, which may thus result in alternative signal transduction processes and further expand the applications of hybrid organic–inorganic lead halide perovskites and related materials. Considering the toxicity of Pb²⁺ and associated environmental problems, future research will also focus on the synthesis of Pb²⁺-based multifunctional materials with good thermal stability and water stability, to prevent the leakage of Pb²⁺ ion and to realize their practical applications.

Author Contributions

All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The authors gratefully acknowledge the financial support of the Natural Science Foundation of China (21771026), the Hubei Provincial Natural Science Foundation of China (2018CFA047), and the Natural Science Foundation of Jingzhou (2019EC61-03). Financial support from the Education University of Hong Kong (04567) is also acknowledged.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2021.636431/full#supplementary-material.

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