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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Efficient Pure Blue Light-Emitting Diodes Based on CsPbBr3 Quantum-Confined Nanoplates

Wei Shen,Ye Yu,Wenzhu Zhang,Yanfeng Chen,Jianbin Zhang,Liu Yang,Jingting Feng,Gang Cheng,Lihui Liu,Shufen Chen

Exploitation of next-generation blue light-emitting diodes (LEDs) is the foundation of the revolution in lighting and display devices. Development of high-performance blue perovskite LEDs is still challenging. Herein, 4-aminobenzenesulfonic acid (SA) is introduced to passivate blue CsPbBr3 nanoplates (NPLs), reducing the ionic migration via a more stable Pb2+–SO3–– formation, and the trap state density of films shows a 50% reduction. The inevitable Br– vacancy defects after the multistep washing process can be suppressed by a suitable MABr treatment, which can boost the external quantum efficiency (EQE) performance. It should be noted that the coverage of NPL films is another key factor to realize reproducible pure blue electroluminescence (EL). Therefore, we proposed an alternate droplet/spin coating method to improve the coverage and thickness of NPL layer to prevent hole transport layer emission and increase the reproducibility of LED performance and spectra. Furthermore, we designed hole transport layers to decrease the hole transport barrier and improve the energy-level alignment. According to SA passivation, MABr treatment, alternate droplet/spin coating method, and device structure optimization, a CsPbBr3 NPL-based pure blue (0.138, 0.046) LED with 3.18% maximum EQE can be achieved, and the half-lifetime of EL can be enhanced 1.71 times as compared to that of the counterpart LED without SA. Both performance and stability of pure blue NPL LEDs can be greatly improved via ligand passivation, alternate droplet/spin coating method, and device structure optimization, which is a trend to promote the development of pure blue perovskite LEDs in future.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Rare earth Nd-doping lead-free double perovskite Cs2AgBiBr6 films with improved resistive memory performance

Chongguang Lyu,Chang Liu,Huihua Min,Xinyu Shi,Ran Jiang,Zhikang Ao,Xu Zhang,Chunli Wang,Huifang Ma,Lin Wang

Lead-free double perovskites have been an excellent candidate for resistive memories due to their mixed electronic-ionic properties, remarkable ambient stability and nontoxicity. However, the studies on resistive memories of rare-earth ion doping lead-free double perovskite are scarce to date. Here, we report the lead-free double perovskite Cs 2 AgBiBr 6 films with tuning rare earth Nd 3+ content by the vacuum sublimation and solution processing. The X-ray diffraction (XRD) pattern and scanning electron microscopy (SEM) confirm that Nd-doped Cs 2 AgBiBr 6 films show high crystallinity and phase purity. We also systematically investigate the resistive memory properties of the resulted Cs 2 AgBiBr 6 films doped by different content Nd 3+ . The resistive memory devices demonstrate a typical write-once-read-many-times (WORM) behavior with low on-set voltage and long retention time. Particularly, the ON/OFF ratio of Nd-doped Cs 2 AgBiBr 6 film is 1000 times higher than that of the undoped Cs 2 AgBiBr 6 film. This study exhibits that Nd-doped Cs 2 AgBiBr 6 film provide a new material platform for lead-free perovskite-based application in future electronics and optoelectronics .

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Materials Today Physics · 2022 · IF 11.021

High-efficient yellow-green emission in (TDMP)MnBr4 single crystal with modulation of spin-phonon-charge interactions

Tao Huang,Qilin Wei,Wenchao Lin,Hui Peng,Shangfei Yao,Bingsuo Zou

In this paper, a new zero-dimensional organic-inorganic hybrid manganese bromide single crystal with high-efficiency yellow-green emission has been synthesized by inserting C 6 H 16 N 2 2+ into [MnBr 4 ] 2- tetrahedrons lattice, and its PLQY reaches up to 89%. At the same time, the relationship between the emission wavelength and relaxation process under CW laser excitation was investigated in this single crystal, exhibiting different emission colors under continuous-wave laser excitation of different wavelengths. The results show that the distance between the nearest Mn 2+ in the lattice is 6.8 Å, this number brings up a very weak ferromagnetic coupling state and a dominant paramagnetic state, which lead to a significant emission band at 550 nm and a weak emission band at about 640 nm when excited by 325 nm laser. The high-level d-d transition at about 400 nm and AFM d-d transition at 458 nm band could be found simultaneously under continuous-wave laser excitation above the bandgap, and the photophysical properties of the multiple emission bands and the microscopic interactions of the spin, carrier, and phonon inside the lattice have been discussed. These findings provide a new direction for Mn-based materials in the field of luminescence and provide ideas for the development of new materials with the microscopic interaction modulation of the spin, carrier, and phonon.

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OPTICAL MATERIALS · 2022 · IF 3.754

Perovskite quantum dot-coated YAG:Ce composites for warm white light-emitting diodes

Yun Tang,Ben Liu,Nan Yan,Xiaoqiang He,Hudie Yuan,Yalou Xin,Hongfeng Yin

Widespread application of YAG:Ce-based white light-emitting diodes (WLEDs) is being challenged due to the lack of red emission, leading to their poor color rendering index (Ra) and high correlated color temperature (CCT). Perovskite quantum dots (QDs), presenting high photoluminescence quantum yield and simple fabrication process have been recognized as promising red-emitting component for warm WLEDs. However, conventional method by mechanically mixing QDs with YAG:Ce always results in undesirable dispersion due to their huge size difference. Moreover, the two components display different sinking behavior in silicone , which would further deteriorate the color uniformity of WLED. To address these issues, in this study, red-emitting MAPbBr 3-x I x QDs-coated YAG:Ce (A-YAG@QDs) composites were successfully prepared to further fabricate WLED with compensated red emission. The chemical coordination interactions between QDs and functionalized YAG:Ce make the two components behave as a whole, which effectively avoids the dispersion and sinking-related issues. The WLED, which combined blue LED chip and A-YAG@QDs composite, exhibited warm white light with low CCT of 4474 K, high Ra of 90.1 and high value of saturated red color component R9 as 95. This study demonstrated a promising strategy to prepare QDs-coated phosphor composites for the generation of warm white light for indoor lighting application.

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2022 · IF 24.319

Space-confined growth of lead-free halide perovskite Cs3Bi2Br9 in MCM-41 molecular sieve as an efficient photocatalyst for CO2 reduction at the gas−solid condition under visible light

Zihao Cui,Peng Wang,Yaqiang Wu,Xiaolei Liu,Guoqiang Chen,Peng Gao,Qianqian Zhang,Zeyan Wang,Zhaoke Zheng,Hefeng Cheng,Yuanyuan Liu,Ying Dai,Baibiao Huang

A facile and effective impregnation method is employed to synthesize the space-confined growth of lead-free halide perovskite Cs 3 Bi 2 Br 9 in MCM-41 molecular sieve. This MCM-41 @CBB (Cs 3 Bi 2 Br 9 ) composite shows an outstanding performance for the photocatalytic reduction of CO 2 to CO at the gas−solid condition under visible-light irradiation. The CO production rate of the MCM-41 @ 50 wt% CBB is determined to be 17.24 μmol g −1 h −1 , which greatly exceeds that of pure CBB (1.89 μmol g −1 h −1 ). The composite is highly stable showing no apparent decrease in the catalytic activity after 8 cycles of repeated experiment. The performance of space-confined growth of CBB nanoparticles in the serial molecular sieve exhibits 2.97–13.4 fold higher than that of pure CBB, respectively, which is superb than CPB (CsPbBr 3 ) and MCM-41 @CPB prepared in the same condition. The results are comparable with those reported for many lead halide perovskites, and are in the top among the lead-free perovskites, especially bismuth halide perovskites.

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Advanced Healthcare Materials · 2022 ·Vol. 11 ·期 12 ·2200199 · IF 11.092

Photoactivated Release of Nitric Oxide and Antimicrobial Peptide Derivatives for Synergistic Therapy of Bacterial Skin Abscesses

Maohua Chen,Jingjing Zhou,Pan Ran,Fangmei Lei,Jie Meng,Junwu Wei,Xiaohong Li

It is of paramount importance to develop novel approaches for combating bacterial resistance and the integration of different antibacterial mechanisms is essential to achieve synergistic bactericidal efficiency while reducing the associated side effects. Herein, amphiphilic antimicrobial copolymers derived from poly- l -lysine (PLL), black phosphorus quantum dots (BPQDs) as near-infrared (NIR) sensitizer, and S-nitrosocysteamine (SNO) as nitric oxide (NO) donor, are assembled into PELI@BPQD-SNO nanoparticles through electrostatic interactions. Amphiphilic copolymers with isopentanyl grafts on PLL at a ratio of 50% achieve an optimal balance between antibacterial activity and hemolysis rate. Photothermal effect of BPQDs leads to NIR-responsive release of NO and the combination with amphiphilic copolymers mutually enhances long-term inhibition of bacterial growth. In an S. aureus -infected subcutaneous abscess model, the bactericidal rate of PELI@BPQD-SNO/NIR treatment reaches nearly 99.6%, which is significantly higher than those without NO release (38%) or amphiphilic copolymers (24%) or NIR irradiation (17%). PELI@BPQD-SNO/NIR treatment shows full recovery of infected wounds, efficient retardation of inflammatory cells, and reconstruction of blood vessels similar to those of healthy skin. Therefore, the electrostatic assembly demonstrates a promising strategy to deliver charged therapeutic agents and the photoactivated release of NO and amphiphilic copolymers achieves synergistic antibacterial efficacy without using any antibiotics.

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CRYSTENGCOMM · 2022 ·Vol. 24 ·期 11 ·2100-2106 · IF 3.756

An ion migration induced self-powered photoelectrical detector based on FAPbBr3 single crystals

Song-Tao Dong,Zhuang Fu,Miaocheng Yu,Jia-Ling Jiang,Xiaoyun Jin,Yu-Hang Guo,Lei Wang,Ya-Mei Zhang

Self-powered photoelectric devices as a new type of sensor without an external power source have a great potential advantage in the next generation of portable and wearable personal devices. The design of those devices is normally based on three kinds of strategies: a p–n junction, the Schottky junction and ferroelectric polarization. Here, a novel solution based on ion migration induced self-powered photodetectors was explored. In this work, high quality halide perovskite FAPbBr3 crystals were grown by an inverse temperature crystallization (ITC) method. An irreversible ion migration was intentionally created using a symmetrically structured Au/FAPbBr3/Au device. The resulting built-in electric field and energy band bending were proved using electrical measurements in the dark and under light. Finally, the response of the ion migration induced self-powered FAPbBr3 detector was investigated with the values of R (∼0.18 mA W−1) and EQE (∼0.055%) under light with a power density of 1 mW cm−2 and a wavelength of 397 nm. Our investigation demonstrates that ion migration, which is normally deemed a detrimental factor for device stability, can be intentionally used for self-powered photoelectric devices.

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RSC Advances · 2022 ·Vol. 12 ·期 10 ·6083-6092 · IF 4.036

An efficient modulated synthesis of zirconium metal–organic framework UiO-66

Xia Chen,Yongjie Li,Qiang Fu,Hongyun Qin,Junnan Lv,Kun Yang,Qicheng Zhang,Hui Zhang,Ming Wang

The use of large amounts of deleterious solvents in the synthesis of metal–organic frameworks (MOFs) is one of the important factors limiting their application in industry. Herein, we present a detailed study of the synthesis of UiO-66, which was conducted with hydrobromic (HBr) acid as a modulator for the first time, at a high concentration of precursor solution (ZrCl4 and H2BDC, both 0.2 mol L−1). Powder crystals with atypical cuboctahedron structure were obtained which indicated that the HBr acid modulator played roles by competitive coordination and deprotonation modulation, thereby controlling the processes of nucleation and crystal growth. The properties of the obtained materials were systematically characterized and compared with those of materials synthesized with hydrofluoric (HF) acid and hydrochloric (HCl) acid modulators. Despite the high concentration of defectivity, the UiO-66 material synthesized with the HBr acid additive has the characteristics of larger specific surface area, excellent thermal stability and higher porosity in the structure. Besides that, the present protocol has the advantages of high reaction mass efficiency (RME), and feasibility of scalable synthesis, providing a facile and sustainable route to diverse Zr-based MOFs.

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SENSORS AND ACTUATORS B-CHEMICAL · 2022 · IF 9.221

Au@Ag@ZIF-8 multifunction probe with internally o-phenylenediamine encoding for the colorimetric, fluorescence, and SERS multi-mode optical detection of reactive sulfur species

Xia Zhou,Xiaoling Lin,Haiqiu Huang,Ping Li,Jiamin Wu,Xueqin Huang,Huaihong Cai,Hai Han,Junxia Zheng,Haibo Zhou

Visual, highly selective, and sensitive detection of sulfur dioxide (SO 2 ) and its derivatives (SO 3 2- ) in vitro/in vivo is of great significance in maintaining cell homeostasis. A new Au@Ag@ZIF-8 optical sensor with o-phenylenediamine (OPD) internal coding surface-enhanced Raman scattering (SERS) tags based on the free radical reaction was synthesized for multi-mode detection of sulfite . First, Co 2+ is oxidized to Co 3+ . Second, the oxidoreduction between SO 3 2- and Co 3+ produces SO 4 -• and Co 2+ to complete the cycle. The resulting SO 4 -• is further reacted with the chromogenic substrate OPD to form the polymer. Due to the UV–vis absorbance of OPD polymer being stronger than that of OPD, but the fluorescence intensity is lower, and their Raman peaks are obviously different, this sensor can be used for the detection of SO 3 2- through colorimetric, fluorescence, and Raman multi-mode. The main advantages are as follows: (1) high selectivity; (2) achieve fast, visual, and highly sensitive detection of SO 3 2- , and the low limit of detection (LOD) is 1 nM; (3) improve the reliability of detection and expands the detection range (1 nM-800 μM); (4) demonstrate the applicability in recognizing SO 3 2- in HeLa cells to provide accurate information on the dynamic distribution of sulfur in cells.

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ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE · 2022 ·Vol. 648 ·期 8 ·e202100334 · IF 1.414

Structural Evolution and Photoluminescence Properties of Two-dimensional Lead Halide Perovskites

Yue-Yu Ma,Hong-Mei Pan,Dong-Yang Li,Shuang Wu,Zhihong Jing

Herein, by using different size of organic molecules as cation templates, we prepared four new two-dimensional (2D) lead halide perovskites, [PrPipz]PbBr 4 ( 1 ), [DMEDA]PbBr 4 ( 2 ), [TMEDA] 0.5 [DMA]PbCl 4 ( 3 ) and [TMA] 4 Pb 3 Cl 10 ( 4 ). Under the distinct structural directing effects of organic cations, compounds 1–4 present four different types of 2D inorganic layers. Remarkably, compounds 1 , 3 and 4 exhibit broadband blue emissions, while compound 2 exhibits broadband yellow emission upon the excitation of UV light at room temperature. This work paves a way to modulate the crystal structure and photoluminescent property of low-dimensional halide perovskite via structural modulation strategy from the molecular level.

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Journal of Physical Chemistry C · 2022 · IF 4.177

Excitation-Power-Dependent Emission Color Tuning in Mn-Doped One-Dimensional Perovskite Single Crystal

Zhaoxia Yang,Wenming Tian,Fengke Sun,Shengye Jin,Dongjiang You

One-dimensional (1D) perovskites are ideal broadband-emitting phosphors for white-emitting diode applications. Doping Mn2+ in 1D perovskites provides a new idea to tune the materials’ light-emitting properties. Here, we report an excitation-power-dependent dual-band emission from both self-trapped excitons (STEs) and Mn dopants in individual 1D Mn-doped DMEDAPbBr4 single crystals. By changing the excitation intensity, we realize a broad and continuous color tuning range between blue and orange. The temperature-dependent photoluminescence (PL) and transient spectroscopy measurements demonstrate that the tunable emission color is enabled by the competitive transfers of excitons to the STE state and Mn2+ ions. The Mn-doped 1D perovskites exhibit a high photostability by showing a continuous switch between blue and orange emissions during an uninterrupted operation time of 7.5 h. The high stability and emission-color switchable properties make the Mn-doped 1D perovskites special optically tunable PL materials for potential light-emitting applications.

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CRYSTAL GROWTH & DESIGN · 2022 · IF 4.01

Crystalline Covalent Organic Frameworks Based on Mixed Metallo- and Tetrahydroporphyrin Monomers for Use as Efficient Photocatalysts in Dye Pollutant Removal

Chenxi Liu,Minghui Chen,Hongrui Li,Quan Shi,Yaqing Feng,Bao Zhang

Unique features, including a high specific surface area, great stability, and crystallinity, make covalent organic frameworks (COFs) intriguing sorbents and catalysts in light-driven water pollutant degradation. Inspired by the light absorption capability of porphyrin derivatives and the carrier separation ability of a donor–acceptor (D–A) configuration, we constructed two-dimensional porphyrin donor-based D–A COFs: COF-HTBD involving only tetrahydroporphyrins and COF-HMTBD (M = Co, Fe, Cu) involving both tetrahydro- and metalloporphyrins via a mixed porphyrin monomer strategy. The monomer 2,1,3-benzothiadiazole-4,7-dicarboxaldehyde (BD) is incorporated as an electron accepting moiety. Interestingly, COF-HTBD, COF-HCuTBD, and COF- HFeTBD exhibit staggered stacking, while the stacking model of COF-HCoTBD transforms from staggered to eclipsed. Notably, COF-HFeTBD demonstrates excellent activities and stabilities toward visible light-driven photocatalytic rhodamine B (RhB) degradation in aqueous solutions with H2O2 present (100% removal in 3 h). Overall, this work provides an interesting strategy for the construction of D–A-type porphyrin COFs for dye pollutant removal.

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