Publications by authors named "Peigeng Han"

Zero-dimensional (0D) metal halides have emerged as excellent luminescent materials for optical and optoelectronic applications. Especially environmentally friendly ternary zinc halides have recently drawn increasing attention. Herein, we present the codoping of Cu and Mn ions into 0D CsZnBr single crystals (SCs), which show bright PL emission and high stability.

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Metal halide perovskite materials with excellent carrier transport properties have been regarded as a new class of catalysts with great application potential. However, their development is hampered by their instability in polar solvents and high temperatures. Herein, we report a solution-processed CsMoCl perovskite nanocrystals (NCs) capped with the Mo, showing high thermostability in polar solvents.

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Metallosalen-covalent organic frameworks have recently gained attention in photocatalysis. However, their use in CO photoreduction is yet to be reported. Moreover, facile preparation of metallosalen-covalent organic frameworks with good crystallinity remains considerably challenging.

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Metal halide nanocrystals (NCs) with high photoluminescence quantum yield (PLQY) are desirable for lighting, display, and X-ray detection. Herein, the novel lanthanide-based halide NCs are committed to designing and optimizing the optical and scintillating properties, so as to unravel the PL origin, exciton dynamics, and optoelectronic applications. Sb-doped zero-dimensional (0D) Cs TbCl NCs exhibit a green emission with a narrow full width of half maximum of 8.

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Inorganic halide double perovskite (DP) nanocrystals (NCs) have attracted great attention because of their nontoxicity, mild reaction conditions, good stability, and excellent optical and optoelectronic properties. Herein, we prepare the inorganic terbium halide DP CsBTbCl (B = Na or Ag) NCs with bright green photoluminescence (PL) emission. The Na-Tb-based DP NCs exhibit better PL properties compared with the Ag-Tb-based DP NCs, which is due to CsNaTbCl NCs having a more localized charge carrier distribution on the [TbCl] octahedron.

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Lead-free metal halide nanocrystals (NCs) have aroused increasing attention due to their unique optoelectronic properties based on localized excitons (LEs). However, the vital influencing factors for the LEs based photoluminescence (PL) are still not well-understood due to the coupling of various intrinsic and extrinsic factors of the NCs. Herein, by engineering the phase, size, morphology, and chemical composition, we are able to decouple the intrinsic and extrinsic factors of manganese doped cesium zinc-halide NCs.

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Lead halide perovskites have achieved remarkable success in various photovoltaic and optoelectronic applications, especially solar cells and light-emitting diodes (LEDs). Despite the significant advances of lead halide perovskites, lead toxicity and insufficient stability limit their commercialization. Lead-free double perovskites (DPs) are potential materials to address these issues because of their non-toxicity and high stability.

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Combining steady-state photoluminescence and transient absorption (TA) spectroscopy, we have investigated the photoinduced charge transfer dynamics between lead-free Mn-doped CsNaInBiCl double perovskite (DP) nanocrystals (NCs) and conjugated poly[2-methoxy-5-(3',7'-dimethyloctyloxy)-1,4-phenylenevinylene] (MDMO-PPV). Upon ultraviolet-A excitation, the photoinduced absorption feature of DP NCs/MDMO-PPV nanocomposites disappeared, and the stimulated emission weakened in the TA spectrum. This was due to charge transfer from the MDMO-PPV polymers to DP NCs.

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Double perovskites (DPs) are one of the most promising candidates for developing white light-emitting diodes (WLEDs) owing to their intrinsic broadband emission from self-trapped excitons (STEs). Translation of three-dimensional (3D) DPs to one-dimensional (1D) analogues, which could break the octahedral tolerance factor limit, is so far remaining unexplored. Herein, by employing a fluorinated organic cation, we report a series of highly luminescent 1D DP-inspired materials, (DFPD) M InBr (DFPD=4,4-difluoropiperidinium, M =K and Rb ).

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Lead-free halide double perovskites (DPs) have attracted great attention due to their stability, nontoxicity and good photophysical property. In this work, we report a new, small-bandgap CsCuSbCl DP nanocrystals (NCs) with a bandgap of 1.66 eV, which is the smallest bandgap in reported lead-free three-dimensional DP NCs.

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Lead-free halide perovskite nanocrystals (NCs) have recently attracted attention due to their nontoxicity and stability as alternatives to lead-based perovskite NCs. Here, we report undoped and manganese-doped all-inorganic, lead-free double perovskite (DP) NCs: CsNaIn Bi Cl (0 < < 1) and CsNaIn Bi Cl:Mn (0 ≤ ≤ 1) NCs. Undoped NCs exhibit blue emission.

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Zero-dimensional (0D) lead-free perovskites have unique structures and optoelectronic properties. Undoped and Sb-doped all inorganic, lead-free, 0D perovskite single crystals A InCl (H O) (A=Rb, Cs) are presented that exhibit greatly enhanced yellow emission. To study the effect of coordination H O, Sb-doped A InCl (A=Rb, Cs) are also synthesized and further studied.

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Lead-free halide perovskite nanocrystals (NCs) have drawn wide attention for solving the problem of lead perovskites toxicity and instability. Herein, we synthesize the direct band gap double perovskites undoped and Ag-doped Cs NaInCl NCs by variable temperature hot injection. The Cs NaInCl NCs have little photoluminescence because of dark self-trapped excitons (STEs).

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Lead-free perovskite nanocrystals (NCs) were obtained mainly by substituting a Pb cation with a divalent cation or substituting three Pb cations with two trivalent cations. The substitution of two Pb cations with one monovalent Ag and one trivalent Bi cations was used to synthesize Cs AgBiX (X=Cl, Br, I) double perovskite NCs. Using femtosecond transient absorption spectroscopy, the charge carrier relaxation mechanism was elucidated in the double perovskite NCs.

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