Publications by authors named "Kezhao Du"

The glassy state of inorganic-organic hybrid metal halides combines their excellent optoelectronic properties with the outstanding processability of glass, showcasing unique application potential in solar devices, display technologies, and plastic electronics. Herein, by tailoring the organic cation from -phenylpiperazine to dimethylamine gradually, four types of zero-dimensional antimony halides are obtained with various optical and thermal properties. The guest water molecules in crystal (-phenylpiperazine)SbCl·Cl·5HO lead to the largest distortion of the Sb-halogen unit, resulting in the red emission different from the yellow emission of other compounds.

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The strategy of organic ligand exchange is proposed to tune the optical properties of organic-inorganic hybrid cuprous halides. In this work, the chiral ligand (S)-(-)-2,2'-bis(di--tolylphosphino)-1,1'-binaphthyl ((S)-Tol-BINAP) and achiral triphenylphosphine (PPh) are introduced into cuprous halides CuX-PPh-[(S)-Tol-BINAP] (X = Cl, Br, I) through organic ligand exchange. As a result, the mixed organic ligands can enhance second harmonic generation (SHG) and aggregation-induced emission (AIE) optical properties.

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Vacancy-ordered perovskites and derivatives represent an important subclass of hybrid metal halides with promise in applications including light emitting devices and photovoltaics. Understanding the vacancy-property relationship is crucial for designing related task-specific materials, yet research in this field remains sporadic. For the first time, we use the Connolly surface to quantitatively calculate the volume of vacancy (V□, □=vacancy) in vacancy-ordered double perovskite derivatives (VDPDs).

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Anisotropy is crucial for birefringence (Δn) in optical materials, but optimizing it remains a formidable challenge (Δn >0.3). Supramolecular frameworks incorporating π-conjugated components are promising for achieving enhanced birefringence because of their structural diversity and inherent anisotropy.

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Herein, the first F-containing iodate-phosphate, namely BaGaF(IO)(PO), was prepared a hydrothermal reaction, in which HPF (70 wt% solution in water) was used as the source of both fluoride and phosphate anions for the first time. BaGaF(IO)(PO) features an unprecedented 1D [GaF(IO)(PO)] helix chain, composed of a 1D Ga(1)(IO)OF chain the bridging of 0D Ga(2)(PO)F. The UV-Vis spectrum shows that BaGaF(IO)(PO) has a wide bandgap with a short-UV absorption edge (4.

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van der Waals (vdW) superlattices, comprising different 2D materials aligned alternately by weak interlayer interactions, offer versatile structures for the fabrication of novel semiconductor devices. Despite their potential, the precise control of optoelectronic properties with interlayer interactions remains challenging. Here, we investigate the discrepancies between the SnS/TiS superlattice (SnTiS) and its subsystems by comprehensive characterization and DFT calculations.

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Using copper-ionophores to translocate extracellular copper into mitochondria is a clinically validated anticancer strategy that has been identified as a new type of regulated cell death termed "cuproptosis." This study reports a mitochondria-targeting Cu(I) complex, Cu(I)Br(PPh) (CBP), consisting of a cuprous ion coordinated by three triphenylphosphine moieties and a Br atom. CBP exhibited antitumor and antimetastatic efficacy and by specifically targeting mitochondria instigating mitochondrial dysfunction.

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With the rapid development of white LEDs, the research of new and efficient white light emitting materials has attracted increasing attention. Zero dimensional (0D) organic-inorganic hybrid metal halide perovskites with superior luminescent property are promising candidates for LED application, due to their abundant and tailorable structure. Herein, [(CH)S]SnCl·HO is synthesized as a host for dopant ions Bi and Sb.

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Lead-based two-dimensional organic-inorganic hybrid perovskites (2D HOIPs) are popular materials with various optical properties, which can be tuned through metal ion doping. Due to the size and valence misfit, metal ion dopants in 2D lead-based HOIPs are still limited. In this work, Mn, Sb and Bi are doped into 2D (HDA)PbBr (HDA = protonated dopamine) successfully.

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Article Synopsis
  • Two different isomeric forms of indium bromide crystals, α and β, were created by altering cooling conditions during their synthesis.
  • Structural differences reveal varied supramolecular interactions, supported by Hirshfeld surface analysis.
  • The α form exhibits a significantly higher photoluminescence quantum yield due to its compact structure and effective electron transfer processes, offering insights for future design of luminescent indium-based materials.*
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In this study, we identify a novel class of second-order nonlinear optical (NLO) crystals, non-π-conjugated piperazine (HCN, PIP) metal halides, represented by two centimeter-sized, noncentrosymmetric organic-inorganic metal halides (OIMHs), namely HCNCdI (222) and HCNCdI (). HCNCdI is the first to be prepared, and its structure contains a CdI tetrahedron, which led to a poor NLO performance, including a weak and non-phase-matchable second harmonic generation (SHG) response of 0.5 × KHPO (KDP), a small birefringence of 0.

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Metal ion-doped zero-dimensional halide perovskites provide good platforms to generate broadband emission and explore the fundamental dynamics of emission regulations. Recently, Sb-doped zero-dimensional halide perovskites have attracted considerable attention for the high quantum yield of yellow emission; however, the triplet state recombination is activated and the singlet state emission is usually absent. Herein, we fabricate an Sb-doped zero-dimensional [(CH)N]SnCl perovskite that can induce singlet and triplet emission.

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Zero-dimensional organic-inorganic metal halide hybrids provide ideal bulk-crystal platforms for exploring the pressure engineering of electron-phonon coupling (EPC) and self-trapped exciton (STE) emission at the molecular level. However, the low stiffness of inorganic clusters hinders the reversible tuning of these physical properties. Herein, we designed a Sb-doped metal halide with a high emission yield (89.

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Article Synopsis
  • Bismuth-halide-based inorganic-organic hybrid materials (Bi-IOHMs) are promising for luminescence applications because they are low in toxicity and chemically stable.
  • Two specific Bi-IOHMs, [Bpy][BiCl(Phen)] and [PP14][BiCl(Phen)]·0.25HO, were synthesized and characterized, revealing distinct structural features through single-crystal X-ray diffraction and photoluminescent properties under UV light.
  • The differences in their ionic liquid components resulted in varying rigidity and photoluminescence quantum yield, with implications for improved luminescence and temperature sensing capabilities.
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Recently zero-dimensional (0-D) inorganic-organic metal halides (IOMHs) have become a promising class of optoelectronic materials. Herein, we report a new photoluminescent (PL) 0-D antimony(III)-based IOMH single crystal, namely [HBPZ][SbCl]·HO (BPZ = benzylpiperazine). Photophysical characterizations indicate that [HBPZ][SbCl]·HO exhibits singlet/triplet dual-band emission.

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Intricate superstructures possess unusual structural features and promising applications. The preparation of superstructures with single-crystalline nature are conducive to understanding the structure-property relationship, however, remains an intriguing challenge. Herein we put forward a new hierarchical assembly strategy towards rational and precise construction of intricate single-crystal superstructures.

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Polydopamine (PDA) is a good adhesion agent for lots of gels inspired by the mussel, whereas hybrid organic-inorganic perovskites (HOIPs) usually exhibit extraordinary optoelectronic performance. Herein, mussel-inspired chemistry has been integrated with two-dimensional HOIPs first, leading to the preparation of new crystal (HDA)PbBr () (DA = dopamine). The organic cation dopamine can be introduced into PDA resulting in a thin film of (HPDA)PbBr ().

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Herein, two novel metal iodate-fluorides, ZrF(IO) and RbGaF(IO), have been prepared hydrothermal reactions. In the structure of ZrF(IO), neighboring Zr atoms are connected a pair of F atoms into the one-dimensional (1D) [ZrF] cationic chain, which further attaches two iodate groups forming 1D ZrF(IO), whereas the 1D cationic chain in RbGaF(IO) is [GaF], formatted by the bridging of Ga cations and axial F anions, which further connect with one iodate group and two terminal F anions into 1D [GaF(IO)] anionic chains. According to the experimental characterization and theoretical calculations, both of them exhibit wide bandgaps (4.

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Article Synopsis
  • Zero-dimensional organic-inorganic metal halides (OIMHs), particularly hybrid antimony(III) bromides (HABs), have potential for high photoluminescence quantum yields (PLQYs), but current values are lower compared to their chloride counterparts.* -
  • Researchers developed a method to enhance PLQYs by synthesizing two structurally similar HABs with different solvent molecules, resulting in notable differences in their emission properties and PLQYs, specifically a nearly twofold increase in PLQY for one compound.* -
  • The improvement in PLQY is linked to structural changes influenced by hydrogen bonding between the inorganic components and solvent molecules, underscoring the importance of structural rigidity in optimizing the phot
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Article Synopsis
  • The compound [Cmim][Mim][SbCl] features dual cations and is the first to demonstrate deep-red emission in zero-dimensional organic-inorganic hybrid materials.
  • The emission is attributed to significant anion distortion caused by imbalanced supramolecular interactions.
  • This results in a remarkably large Stokes shift of 335 nm and a full width at half maximum (FWHM) of 210 nm in the emission spectrum.
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Article Synopsis
  • Zero-dimensional metal halides, particularly [EtPPh][SbCl], are gaining interest for their ability to switch luminescence, making them useful for sensors and anticounterfeiting.
  • Research showed that only solvent molecules with a volume less than 22.3 Å can interact with [EtPPh][SbCl], influencing their photoluminescent properties.
  • The study further revealed that solvent functional groups affect the hydrogen bonding strength with [SbCl], leading to changes in luminescent behavior and enhancing overall photoluminescence quantum yield to 95%.
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Although luminescent indium(III) based halide perovskites have been widely investigated, the study of emissive indium(III) halide hybrids is limited. Three indium(III) chloride hybrids based on a bpym ligand were synthesized, namely [EPy][InCl(bpym)InCl]·DMF (1), [EPy][InCl(bpym)InCl] (2), and [BPy][InCl(bpym)InCl] (3) (EPy = -ethylpyridinium; BPy = -butylpyridinium; bpym = 2,2'-bipyrimidine). They all exhibit a zero-dimensional structure, in which the ligand bpym interconnects two [InCl] to form a [InCl(bpym)InCl] anion that is further charge-compensated by the corresponding pyridinium cations.

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A promising anode material consisting of bimetallic thiophosphate Zn Co PS and CoS with 2D/3D heterostructure is designed and prepared by an effective chemical transformation. Density functional theory calculations illustrate that the Zn can effectively modulate the electrical ordering of Zn Co PS on the nanoscale: the reduced charge distribution emerging around the Zn ions can enhance the local built-in electric field, which will accelerate the ions migration rate by Coulomb forces and provide tempting opportunities for manipulating Li storage behavior. Moreover, the merits of the large planar size enable Zn Co PS to provide abundant anchoring sites for metallic CoS nanocubes, generating a 2D/3D heterostructure with a strong electric field.

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