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RSC Advances · 2017 ·Vol. 7 ·期 38 ·23415-23421 · IF 3.108

A novel MoS2-based hybrid film as the back electrode for high-performance thin film solar cells

Sheng Yuan,Ming-Jian Zhang,Xiaoyang Yang,Zongwei Mei,Yongji Chen,Feng Pan

MoS2, a representative two-dimensional transition metal dichalcogenide, gains significant interest due to its unique layered structure and electronic structure. In this work, a novel MoS2-based hybrid thin film was constructed by disordered stacking of MoS2–NMP hybrid particles, which were mainly composed of MoS2(NMP)3 molecules stacking in a nearly-parallel manner through S⋯H–C hydrogen bonds. Interestingly, it presents a higher work function (5.42 eV) than Au (5.32 eV), and a unique thickness-dependent conductivity with p-type semiconductor characteristic. Using it as the back contact of CdTe solar cells, the efficiency was improved by 2.6% compared to the traditional cells, mainly from the great improvement in short-circuit current density (Jsc). This significant improvement in solar performance was ascribed to the matchable energy levels at the CdTe/MoS2-based thin film interface and its unique thickness-dependent conductivity. This work opens a new direction for the extensive applications of TMD-based materials.

研究领域: 材料科学 · 光伏技术 · 纳米材料 · 半导体物理 · 表面科学 · 能源材料
✓ 已验证 DOI 高影响因子
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CRYSTENGCOMM · 2024 ·Vol. 27 ·期 5 ·661-667 · IF 2.6

Achieving cuprous iodide hybrid materials with long luminescence lifetimes and high internal quantum yields via aggregation-induced emission

Zhen-Dong Xue,Yi Zhang,Hao-Yu Zhu,Juan-Juan Shao,Qiang Gao,Fang-Ming Wang

Herein, four new cuprous iodide hybrid materials 1–4 were synthesized at room temperature using two types of ligands: imidazoles and triphenylphosphine. Photoluminescence results showed that all the materials exhibited blue emissions with high internal quantum yields (IQYs) ranging from 51% to 64%. Surprisingly, the introduction of triphenylphosphine induced strong aggregation-induced emission (AIE). Additionally, the luminescence lifetimes of these materials were significantly longer, ranging from 11.53 μs to 24.33 μs, which is much longer than those of previous materials. These findings suggest that these materials could be potential candidates for non-rare earth element (REE) lighting phosphors.

研究领域: 材料化学 · 光物理 · 无机-有机杂化材料 · 发光材料 · 非稀土磷光体
✓ 已验证 DOI 高影响因子
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RSC Advances · 2017 ·Vol. 7 ·期 82 ·52024-52029 · IF 3.108

Modulating molecular structures and dielectric transitions in organic–inorganic hybrid crystals

Xiao-Fen Sun,Zhongxia Wang,Wei-Qiang Liao,Peng-Fei Li,Jixing Gao,Yi-Yang Huang,Hai-Peng Chen,Heng-Yun Ye,Yi Zhang

In this paper, three new hybrid phase transition compounds, [Hmpy]CdBr3 (1, Hmpy = N-methylpyrrolidinuium cation), [Hmpy]2CdBr4 (2) and [Hmpy]3CdBr3·CdBr4 (3), were synthetized by means of regulating the ratio of reactants. Systematic characterizations consisting of variable temperature X-ray single crystal diffraction, differential scanning calorimetry (DSC) and dielectric measurements reveal that 1 with infinite one-dimensional (1D) [CdBr3]n− chains undergoes a phase transition around 278 K; 2 with isolated [CdBr4]2− tetrahedrons exhibits a high-temperature phase transition close to 367 K, accompanied by prominent switchable dielectric behavior. Interestingly, 1D [CdBr3]n− chains and isolated [CdBr4]2− tetrahedrons both exist in 3, associated with a phase transition at 320 K. The phase transitions in the three compounds are originated from the order-disorder transitions of the Hmpy cation. It is expected that our finding would promote the development of hybrid dielectric transition materials with adjustable properties.

研究领域: 材料化学 · 凝聚态物理 · 晶体工程 · 功能材料 · 介电材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2022 · IF 9.965

Interfacial architecting of organic–inorganic hybrid toward mechanically reinforced, fire-resistant and smoke-suppressed polyurethane composites

Pingfan Xu,Yaofa Luo,Peikun Zhang

Polyurethane (PU) composites integrated with outstanding fire retardancy, smoke suppression as well as ameliorated mechanical property is attractive, but remains a challenge. Here, we demonstrate the interfacial architecting of organic–inorganic hybrid (ACAPP) by reacting renewable chitooligosaccharide (COS) with ammonium polyphosphate (APP) and ammonium octamolybdate (AOM) via a one-pot, facile and eco-friendly approach. The ACAPP with multiple hydroxyl groups shows good compatibility and strong interfacial adhesion force with PU matrix due to the abundant covalent cross-linking points and hydrogen bonds networks. The incorporation of 15 wt% ACAPP enables the resultant PU composite to achieve a V-0 rating, a limiting oxygen index of 26.1%, 31.1% and 44.8% reduction in total heat release and total smoke production, respectively, far outdistancing conventional APP. The suppressed fire hazards mainly benefits from the synergy catalytic carbonization effect of ACAPP in condensed phase. Moreover, ACAPP reinforces the tensile strength of PU whilst retaining the decent ultimate elongation. This work may offer a referable exemplification for constructing green flame-retardant to balance high fire safety and mechanical properties.

研究领域: 高分子材料科学 · 阻燃化学 · 复合材料工程 · 绿色化学 · 材料界面科学
✓ 已验证 DOI 高影响因子
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POLYHEDRON · 2016 · IF 2.108

Growth, structure, optical and thermal properties of three new organic–inorganic hybrid crystals: (C2H7N4S)3BiCl6·H2O, (C2H7N4S)2BiBr5, and (C2H5N4S)2BiI5

Tongguang Sun,Fei Liang,Xinyuan Zhang,Heng Tu,Zheshuai Lin,Guochun Zhang,Yicheng Wu

Single crystals of three new organic–inorganic hybrid compounds, tri[1-(diaminomethylene)uronium] hexachlorobismuthate ((C 2 H 7 N 4 S) 3 BiCl 6 ·H 2 O, HATU-BCH), bis[1-(diaminomethylene)uronium] pentabromobismuthate, ((C 2 H 7 N 4 S) 2 BiBr 5 , HATU-BB), and bis [3,5-diamino-1,2,4-thiadiazol-2-ium] pentaiodobismuthate ((C 2 H 5 N 4 S) 2 BiI 5 , OHATU-BI), have been successfully grown by slow evaporation method. Their structures were determined by single - crystal X-ray diffraction, in which all anion sublattice structures consist of hexahalobismuthates octahedra with different connection modes involving isolated, shared-corner, and shared-edge. The spectra characters were studied by Infrared and Raman spectra, which interpreted by calculation of the density functional theory (DFT) method and diffuse reflectance spectra. Thermal properties were characterized by thermal gravimetric analysis and differential scanning calorimetry.

研究领域: 材料化学 · 晶体工程 · 配位化学 · 光谱学 · 热分析 · 计算化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY · 2013 ·Vol. 66 ·期 1 ·133-138 · IF 1.66

Preparation of anticorrosion hybrid silica sol–gel coating using Ce(NO3)3 as catalyst

Peng Shusen,Zhao Wenjie,Zeng Zhixiang,Li He,Xue Qunji,Wu Xuedong

In this report, hybrid silica sol–gel coating was prepared using Ce(NO 3 ) 3 (Sol-Ce) as catalyst. Structure, surface morphology and anticorrosion ability of Sol-Ce solution/coating were studied by infrared spectroscopy (IR), scanning electron microscopy, energy dispersive spectrometer (EDS), potentiodynamic scan (PDS) and electrochemical impedance spectroscopy (EIS). IR results showed that Ce(NO 3 ) 3 had a stronger influence on reactivity of alkoxysilane. EDS results revealed that the fraction of Fe in Sol-Ce coating was significantly lower than regular acid-catalyzed hybrid silica sol–gel coating (Sol-Ac) and Sol-Ac with Ce(NO 3 ) 3 -doped coating (Sol-Ac/Ce). The results of PDS and EIS demonstrated that Sol-Ce coating had better anticorrosion ability than Sol-Ac and Sol-Ac/Ce on carbon steel. The enhanced anticorrosion performance of the Sol-Ce coating might result from the following two reasons: (a) Ce(NO 3 ) 3 as a catalyst could alleviate the negative effects of low pH with using acid catalyst (dissolution of carbon steel) and (b) Ce(NO 3 ) 3 could impede corrosion of carbon steel as corrosion inhibitor.

研究领域: 材料科学 · 表面工程 · 腐蚀与防护 · 无机化学 · 电化学
✓ 已验证 DOI 高影响因子
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PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES · 2013 ·Vol. 12 ·期 9 ·1628-1635 · IF 2.923

Novel luminescent hybrids by incorporating rare earth β-diketonates into polymers through ion pairing with an imidazolium counter ion

Li Qiu-Ping,Yan Bing

A series of luminescent polymers are synthesized by incorporating rare earth complex units into polymer matrices. Firstly, we functionalize the selected polymer matrices with the imidazolium moieties, and then introduce the rare earth tetrakis(β-diketonate) complexes into polymer matrices through a mild anion exchange method. The resulting materials are characterized by FTIR, XRD, EDAX, SEM, thermogravimetric analysis, luminescence excitation spectra and emission spectra, luminescence lifetime measurements and diffuse reflectance UV-Vis spectra. The photoluminescence measurements indicate that all these rare earth complex functionalized polymers exhibit a characteristic luminescence emission originating from the corresponding rare earth ions. Among the hybrids, the europium tetrakis(TTA) complex functionalized polymers show remarkable luminescence quantum yields and relatively long 5 D 0 lifetimes at room temperature.

研究领域: 材料化学 · 高分子科学 · 光物理学 · 无机功能材料 · 发光材料
✓ 已验证 DOI 高影响因子
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MATERIALS LETTERS · 2017 · IF 2.572

Synthesis of bioactive polyvinyl alcohol/silica hybrid fibers for bone regeneration

Shu-Hui Xia,Shu-Hua Teng,Peng Wang

Polyvinyl alcohol/silica (PVA/SiO 2 ) hybrid fibers were prepared via a sol–gel combined electrospinning technique, and their potential application in bone tissue engineering was evaluated in terms of in vitro bioactivity. When the PVA concentration was 8%, the obtained PVA/SiO 2 hybrid fibers exhibited a uniform and continuous morphology, with an average fiber diameter of about 542.9 nm. The SiO 2 xerogel phase was uniformly distributed within the PVA matrix, and its actual content was very close to the theoretical value. After 3 days of immersion in simulated body fluid (SBF), the PVA/SiO 2 hybrid fibers displayed a vigorous precipitation of lamellar apatite crystals, reflecting their excellent in vitro bioactivity.

研究领域: 生物材料学 · 组织工程 · 纳米医学 · 生物医学工程 · 无机非金属材料 · 再生医学
✓ 已验证 DOI 高影响因子
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DESALINATION · 2023 · IF 9.9

Enhanced hybrid capacitive deionization performance by the mass balance of electrodes

Xudong Bu,Yurong Zhang,Haiqing Guo,Sheng Wang,Xueyan Du

The ion removal capacity of carbon based capacitive deionization (CDI) is limited by the double-layer mechanism. Replacing one electrode of the conventional carbon-based symmetric CDI with a battery-like ion insertion material to obtain hybrid capacitive deionization (HCDI) can significantly improve the adsorption capacity . Various ion insertion materials have been adopted for HCDI, however, how to optimize the performance of the HCDI system by matching the two electrodes with different ions removal mechanism remains challenging. In this work, a HCDI desalination cell was demonstrated by using NaTi 2 (PO 4 ) 3 /reduced graphene oxide composites (NTP-rGO-700) as the cathode and activated carbon (AC) as the anode. Based on the mass balance strategy of electrodes and the electrochemical behavior of hybrid capacitors with different AC:NTP-rGO-700 mass ratios, the HCDI desalination cell was assembled with the optimal AC:NTP-rGO-700 mass ratio of 2:1. At an operating voltage of 1.6 V and a current density of 125 mA·g −1 , the specific adsorption capacity (SAC) of the HCDI cell can reach 51 mg·g −1 with an average salt adsorption rate (ASAR) of 2 mg·g −1 ·min −1 , and the energy consumption (E m ) is 136.53 kJ·mol −1 . This work provides an efficient approach for developing high performance HCDI cell.

研究领域: 环境科学 · 电化学 · 材料科学 · 水处理技术 · 能源存储
✓ 已验证 DOI 高影响因子
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CERAMICS INTERNATIONAL · 2021 ·Vol. 48 ·期 3 ·3081-3095 · IF 4.527

Advanced high-temperature (RT-1100°C) resistant adhesion technique for joining dissimilar ZrO2 ceramic and TC4 superalloys based on an inorganic/organic hybrid adhesive

Mingchao Wang,Zhaoli Chen,Jingxuan Liu,Zhaojie Feng,Jingfang Zhang,Wenzheng Zhai,Haijun Zhang

To meet the high demand for ceramic/superalloy composite structural components in various fields, an advanced high-temperature adhesion technique was firstly developed by preparing a novel inorganic/organic hybrid adhesive suitable for ZrO 2 and TC4 . Chemical bonding started to work at ∼600°C, and became the crucial bonding mechanism at elevated temperatures. The formation of ZrSiO 4 and Ti 5 Si 3 at the interfaces of two substrates not only increased the interfacial connection strength , but also formed two gradient layers with a size of ∼2 μm to effectively alleviate the difference of composition and performance between the adhesive and substrates. In the temperature range of 500–900°C, the matching degree of CTE among ZrO 2 , adhesive and TC4 is higher, and the maximum difference does not exceed 3×10 -6  K -1 . Meanwhile, the formation of a composite structure containing various ceramics (ZrO 2 , SiC and ZrB 2 ) and intermetallics (Ni–Si, Al–Ni), and the improvement of structural compactness of adhesive from 500 to 900°C greatly improved the bonding strength to the maximum value of 31.4 MPa at 900°C. Also, the adhesive pretreated at 900°C showed good thermal cycling resistance, and the strength was still higher than 15 MPa after 50 cycles. For cured adhesive, when used directly in an extreme environment, it can provide bonding strength not less than 5 MPa in the whole temperature range, indicating that the adhesive possessed potential emergency repair convenience. This work significantly broadened the application of high-temperature-resistant adhesion technology in the connection of dissimilar ceramics and alloys.

研究领域: 材料科学 · 复合材料 · 界面工程 · 高温功能材料 · 连接技术
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2020 ·Vol. 44 ·期 33 ·14103-14107 · IF 3.288

Synthesis, structure and photoluminescence properties of three copper(I) iodide based inorganic–organic hybrid structures with pyrazine derivatives

Chanchan Xu,Le Lv,Dawei Luo,Wei Liu

By using pyrazine derivatives, three different types of copper(I) iodide based inorganic–organic hybrid structures, 1D-CuI(2-mo-pz) (1, 2-mo-pz = 2-methoxy-pyrazine), 2D-CuI(2,3-dm-pz)0.5 (2, 2,3-dm-pz = 2,3-dimethyl-pyrazine), and 2D-Cu2I2(2,5-dm-pz)2 (3, 2,5-dm-pz = 2,5-dimethyl-pyrazine), have been obtained by using a slow-diffusion method. Single crystal and powder X-ray diffraction analyses reveal that these hybrid structures are a one-dimensional (1D) staircase chain based structure, two-dimensional (2D) staircase-chain based structure, and 2D rhomboid dimer based structure, respectively. All of the three compounds show photoluminescence, with the internal quantum yield (IQY) as high as 88.2% for 1. This work provides evidence that for this type of hybrid materials, the structure of the inorganic module could be determined by the selection of the organic ligands and that the substituted group on the organic ligands can influence the luminescence efficiency of the hybrid structures.

研究领域: 无机化学 · 材料化学 · 配位化学 · 光物理 · 功能材料
✓ 已验证 DOI 高影响因子
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Advanced Optical Materials · 2022 ·Vol. 10 ·期 15 ·2200605 · IF 10.05

Highly Reversible Moisture-Induced Bright Self-Trapped Exciton Emissions in a Copper-Based Organic–Inorganic Hybrid Metal Halide

Shaofan Fang,Bo Zhou,Huixia Li,Hanlin Hu,Haizhe Zhong,Henan Li,Yumeng Shi

Metal halide perovskites are promising optoelectronic materials due to their unique luminescent properties. However, their practical application is limited by their poor chemical stability, especially in humid environments. Moisture can cause phase changes or chemical decomposition, resulting in significant fluorescence quenching. In this study, a copper-based organic–inorganic hybrid metal halide (t-BA) 3 Cu 6 I 9 is synthesized (t-BA + is the tert-butyl-ammonium ion (C(CH 3 ) 3 NH 3 + )). This material exhibits water-induced luminescence, and its chemical stability in humid environments is being investigated. Tetragonal t-BA 3 Cu 6 I 9 is not luminescent, but it reacts quickly with water in the air. The resultant (t-BA) 2 Cu 2 I 4 ·H 2 O has a broad green emission peak at 520 nm, high photoluminescence quantum yield of 59.4%. Remarkably, (t-BA) 2 Cu 2 I 4 ·H 2 O is converted back to t-BA 3 Cu 6 I 9 at temperatures above 40 °C. This phase conversion is highly repeatable, and the luminescent intensity can be fully recovered after 50 transformation cycles. The mechanism of luminescence is investigated through temperature-dependent photoluminescence spectra and theoretical calculation, which suggests that (t-BA) 2 Cu 2 I 4 ·H 2 O has a more localized charge distribution and sufficient polyhedral distortion, resulting in a bright and efficient emission from self-trapped excitons. This is the first report of water-induced luminescence in copper-based metal halides, and it paves the way for stable luminescent materials that are responsive to humidity.

研究领域: 材料化学 · 光物理学 · 无机化学 · 功能材料 · 发光材料
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