JOURNAL OF MOLECULAR STRUCTURE
·
2023
·
IF 3.8
ChuanYu Lan,Yuandong Wu,Dajiang Mei,Shaoguo Wen,Thomas Doert
Three new complexes, namely (5,7-Dichloro-8-hydroxyquinoline)PbX (X=Br, I) ( 1, 2 ) and Pb2(5,7-Dichloro-8-hydroxyquinoline)4 ( 3 ), were synthesized through solvent evaporation at ambient temperature. The crystal structures and fluorescence emission properties of these complexes were systematically investigated. An analysis using single crystal X-ray diffraction revealed that complexes 1 - 3 form pseudo-dimeric structures through the interaction between lead and neighboring oxygen via secondary contacts. A comparison between the structures of complex 2 and [Pb(μ-Q)I] 2 , a complex of PbI 2 with 8-hydroxyquinoline, showed that the coordination polyhedron changed from a triangular pyramid to a distorted tetrahedron. This change may be attributed to the site resistance effect of the chlorine substituents coordinated to the quinoline ring. Complex 3 has a layered structure formed through secondary contacts and intramolecular hydrogen bonding C-H⋯O and C-H⋯Cl among the lamellar molecules. The maximum emission peak at 489 nm, 505 nm, and 543 nm for complex 1-3 can be assigned to the ligand-to-metal charge transfer (LMCT). The maximum emission peaks were red-shifted by 22 nm, 38 nm, and 75 nm, respectively, compared to the ligand. The number of ligands increases the conformational rigidity of the structure and the electron density on lead atoms causing the molecular structure to change, the energy alters, and the fluorescence peaks to move in the long-wave direction.
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ACS Applied Energy Materials
·
2023
·
IF 6.4
Mingzhe Zhang,Wenhui Li,Wenning Zhao,Xiuxun Han
The carbon-electrode-based CsPbI2Br perovskite solar cells (C-PSCs) are promising photovoltaic technology because of their enhanced stability and low cost. However, the CsPbI2Br film suffers from uneven surface morphology with stripes and the defect-rich surface, which are detrimental to the charge carrier transport between perovskite and carbon. Here, we demonstrate that the formation of stripes is directly related to the I/Br homogenization process during annealing. By introducing a pre-annealing treatment before high temperature annealing, the I/Br homogenization process is modulated and the stripe is successfully wiped off. Besides, enhanced charge carrier transport in the C-PSCs is achieved. Oleic acid (OA) is then introduced to modify the stripe-free perovskite film surface. It is revealed that the carboxyl group in the OA molecule can passivate the undercoordinated Pb ions, leading to further improved charge carrier transport. Eventually, a power conversion efficiency (PCE) of 15.57% is achieved, which is among the highest PCE for the CsPbX3-based C-PSCs. This work demonstrates that combining surface planarization with surface passivation is an effective strategy for developing highly efficient C-PSCs.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Dingliang Dai,Jianhao Qiu,Guanglu Xia,Yong Tang,Zhonghao Wu,Jianfeng Yao
Core-shell Bi-MOF@BiOX (X = I, Br and Cl) hybrids were fabricated by a one-pot solvothermal strategy via regulating the concentration and type of halogen ions in the Bi-based CAU-17 synthesis. By virtue of the competitive coordination effect to Bi 3+ between CAU-17 and BiOX, CAU-17 was converted into another Bi-MOF with similar structures and compositions. Moreover, Bi 3+ plays the role of “bridge” and endows an intimate interface contact between BiOX and the Bi-MOF, which immensely expedites the charge and mass transportation. The obtained Bi-MOF@BiOX hierarchical heterostructures were applied to photocatalytic elimination of solo and mixed pollutants (Cr(VI)/tetracycline and Cr(VI)/o-nitrophenol), and exhibited favorable performances. Choosing Bi-MOF@BiOI as a typical example, the corresponding performances for Cr(VI) reduction, tetracycline and o-nitrophenol degradation in their solo systems are 14, 10, 8 times higher than those of CAU-17, and 13, 7, 5 times higher than those of BiOI under visible light, respectively. Of note, the above photocatalytic performances could be further improved in the coexisting environment of Cr(VI) and tetracycline or o-nitrophenol, which is attributed to the elevated charge separation efficiency caused by the timely consumption of photo-excited electrons and holes. This work gives some insights into the delicate design of MOF photocatalysts and their applications in environmental restoration.
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Nanoscale
·
2023
·Vol. 15
·期 17
·7803-7811
·
IF 6.7
Tian Sun,Tong Chen,Jiahao Chen,Qiang Lou,Zihao Liang,Guijun Li,Xiaoyun Lin,Guoshen Yang,Hang Zhou
Despite the impressive developments in perovskite optoelectronic devices, their long-term stability remains a major challenge. Chemical reactions and ion exchange at the metal/perovskite contact interface are two significant factors that lead to the failure of perovskite devices. To address this issue, a titanium nitride (TiN) layer is introduced as a robust corrosion-resistant coating between perovskite films and metal electrodes. By introducing TiN layer, a perovskite photodiode with dark current down to 3.25 × 10−11 A cm−2 is realized. Consequently, the TiN-based perovskite photodiode shows a specific detectivity of 1.21 × 1014 cm W−1 Hz1/2, which is approximately two orders of magnitude higher than that of the control device without a TiN layer. Under continuous illumination of a 520 nm green light for 576 000 cycles, the responsivity of the TiN-based photodetector remains at 94.27% of its initial value. The TiN-based photodetector exhibits superior stability under thermal stress. After aging at 85 °C for 572 h, the TiN-based photodetector retains 72% of its initial responsivity. Using the TiN-based photodiode, a perovskite image sensor containing 64 × 64 pixelated perovskite photodiodes is constructed over an amorphous silicon thin-film transistor (TFT) backplane. The perovskite image sensor exhibits real-time imaging capability and long-term stability for over 6 months. This study highlights the importance of using metallic nitrides to achieve high-performance and air-stable perovskite devices for optoelectronic applications.
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高影响因子
DESALINATION
·
2023
·
IF 9.9
Qingyi Wang,Yongping Dong,Junmei Ma,Huimin Wang,Xuping Xue,Chaojie Bai,Mingjie Lin,Lingping Luo,Congjie Gao,Lixin Xue
Polyamide/polyethylene thin film composite (PA/PE-TFC) NF membranes were prepared from reverse-phase interface polymerization (RIP) for improved Mg(II)/Li(I) separation. RIP processes between 1,3,5-benzenetricarbonyl chloride (TMC) in bottom organic phase and piperazine (PIP) in upper aqueous phase were developed to form continuous and intact surface PA separation layers on PE porous substrates thinner than traditional polysulfone (PSF) based substrates. After activation with isopropyl alcohol (IPA), PA/PE-TFC-IPA NF membranes were formed, whose NF performance could be tuned by adjusting the preparation conditions. When TMC concentration was kept at 0.15 % w/v, RIP with low PIP concentration (0.025 wt%) yield PA/PE-TFC-IPA NF membranes with negatively charged surfaces , high Na 2 SO 4 rejection rate (95 % ± 3 %) and water permeance (13–19 L·m −2 ·h −1 ·bar −1 ). RIP with high PIP concentration (0.3 wt%) formed PA/PE-TFC-IPA NF membranes with less negative surfaces, high MgCl 2 rejection rate (94.3 ± 0.7 %), low water permeance (4.8 ± 0.3 L·m −2 ·h −1 ·bar −1 ), and high Mg(II)/Li(I) separation coefficient S Li/Mg (18 ± 1) for 1000 ppm LiCl and MgCl 2 mixed solution. PA/PE-TFC-IPA NF membranes also showed good long-term stability and improved anti-fouling performance for positively charged pollutants, bearing high potential for applications in the lithium extraction processes.
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Advanced Optical Materials
·
2018
·Vol. 7
·期 4
·1801323
·
IF 7.43
Jiarui Hao,Xingyu Qu,Lei Qiu,Guogang Li,Yi Wei,Gongcheng Xing,Hongquan Wang,Chunjie Yan,Ho Seong Jang,Ziyong Cheng,Jun Lin
Currently, poor luminescence stability seriously impedes the practical application of inorganic halide perovskite (CsPbX 3 , X = Cl, Br, and I) quantum dots (QDs) in optoelectronic devices. In present work, CsPbX 3 QDs are successfully assembled on natural mineral halloysite nanotubes (HNTs) for improving the luminescence performances. Monodispersed CsPbX 3 QDs are arranged on two edges of HNTs in a highly ordered manner, which possibly originates from the electrostatic interaction between halogen ion and surface hydroxyl (Sur OH 2 + ) on the section face of HNTs. As expected, the photoluminescence (PL) performances of CsPbX 3 @HNTs nanocomposites are obviously improved. The PL intensity still can be maintained even 80% when working at 100 °C. Almost no emission degradation is observed after storing in an open ambient condition for 28 days. Moreover, the PL intensity also maintains 82% of room temperature (RT) intensity after continuously being illuminated by 365 nm UV lamps for 144 h. Excellent white light with Commission Internationale de l'Eclairage (CIE) chromaticity coordinates (0.34, 0.32) of the white light-emitting diodes (w-LEDs) fabricated by CsPbBr 3 @HNTs, CsPbBr 1.2 Cl 1.8 @HNTs, and CsPbBr 1.2 I 1.8 @HNTs phosphors are achieved. This work opens up a new insight in achieving stable CsPbX 3 QD-based multifunctional materials by designing nanocomposites with natural clay mineral.
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CHEMISTRY OF MATERIALS
·
2018
·
IF 9.89
Fei Li,Ying Liu,Hongliang Wang,Qian Zhan,Quanlin Liu,Zhiguo Xia
The control of surface properties of all inorganic cesium lead halide perovskite (CsPbX3; X = Cl, Br, or I) quantum dots (QDs) is essential to achieve excellent stability and high photoluminescence quantum yields (PLQYs). Herein, a facile method was performed to simultaneously enhance the stability and PLQYs of CsPbX3 QDs by a ZnX2/hexane solution post-treatment. We show that the halogen defect on the surface of CsPbX3 QDs can be treated in a controlled way, whereby the “black dots” that adhered on the surface as observed by transmission electron microscopy have be completely removed, resulting in enhanced stability and photoluminescence. The PLQYs of CsPbCl3, CsPbBr3, and CsPbI3 increased from 4, 58, and 63% to 86, 93, and 95%, respectively, and the origin of the “black dots” as well as their transformation mechanism has been demonstrated. As a result, the poly(dimethylsiloxane) composite films created by encapsulating stable and nearly defect-free green-emitting CsPbBr3, the red-emitting K2SiF6:Mn4+ phosphor, and a blue emission GaN chip were prepared and used to fabricate a remote-type white light-emitting diode device, which exhibits a high luminescence efficiency (≤98 lm/W) and a wide color gamut (∼130% of the National Television Standard Committee standard), suggesting the potential for liquid crystal display backlight application.
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MICROCHIMICA ACTA
·
2018
·Vol. 185
·期 11
·1-10
·
IF 5.705
Zhu Xiang,Wang Jianying,Zhu Yuhua,Jiang Honghao,Tan Di,Xu Ziqiang,Mei Tao,Li Jinhua,Xue Longjian,Wang Xianbao
N,S-co-doped carbon dots (N,S-CDs) were synthesized via a single-step solvothermal process by using sodium lignosulfonate and p-phenylenediamine as carbon/nitrogen/sulfur sources. The N,S-CDs have an average diameter of 2.02 ± 1 nm and display green fluorescence, with excitation/emission peak wavelengths at 380/540 nm for optimal fluorescence. Fluorescence is excitation wavelength-dependent and stable in aqueous salt solutions. The fluorescence of the N,S-CDs is selectively quenched by Fe(III) and Ag(I) ions. These ions can be quantified by fluorometry with a limit of detection of 1.7 μM for Fe(III) ions and 11.6 μM for Ag(I) ions. The N,S-CDs also undergo solvatochromism in that emission is green in water solution but blue in polar organic solvents such as ethanol or N,N-dimethylformamide. The color of fluorescence gradually shifts from green to blue when continuously increasing the fraction of organic solvent in water.
N,S-co-doped carbon dots (N,S-CDs) are synthesized by using sodium lignosulfonate and p-phenylenediamine as C/N/S sources. The N,S-CDs can sensitively detect Fe(III) and Ag(I) ions based on fluorometry, and can be used as a solvatochromic probe.
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高影响因子
WATER RESEARCH
·
2018
·
IF 7.051
Yulin Zhang,Yinan Bu,Jiarui Han,Yan Liu,Baiyang Chen,Xiangru Zhang,Mengting Yang,Yueting Sui
Adsorbable organic halogen (AOX) is a bulk organic parameter conventionally used to indicate all adsorbable halogenated organic disinfection byproducts formed in disinfected water. Analytically, AOX is determined by three sequential steps: 1) concentration and separation of AOX from halides with activated carbon, 2) conversion of AOX into halides with pyrolysis , and 3) quantification of halides via microcoulometry or ion chromatography (IC). Because the approach is relatively costly and cannot effectively recover non-adsorbable compounds, we herein proposed a facile and green pretreatment tool to measure the nonionic portion of total organic halogen (NTOX) with a new three-step approach: 1) separation of NTOX and halides with electrodialysis (ED), 2) conversion of NTOX into halides with ultraviolet, and 3) analysis of halides with IC. To verify this proposal, this study presented the efficiency of ED in separating halides and NTOX under a variety of operational and environmental conditions. The results showed that ED removed ≥98.5% of fluoride, chloride, bromide, and iodide from all tested waters (up to 1000 mg-X/L) within 1.5 h. Meanwhile, ED recovered an average of 87.9% of fourteen small molecular weight model compounds with each at 100 μg/L. By using electrospray ionization-triple quadrupole mass spectrometry, the whole pictures of high molecular weight compounds in a chlorinated drinking water before and after ED pretreatment were compared, which revealed 79.7% and 83.6% recoveries of overall polar chlorinated and brominated compounds, respectively. In addition, the quantity and property of the dissolved organic matter were largely maintained by ED, and the retained organics may be used for later characterization. The study hence presents a novel use of ED as a pretreatment tool to enable subsequent NTOX measurement.
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高影响因子
MICROCHIMICA ACTA
·
2018
·Vol. 185
·期 5
·1-7
·
IF 5.705
Tang Shurong,Wang Meili,Li Guangwen,Li Xin,Chen Wei,Zhang Lan
A hybrid material composed of graphitic carbon nitride (g-C 3 N 4 ) and platinum nanoparticles (PtNPs) with peroxidase mimicking activity was used to design a rapid, sensitive and low-cost colorimetric method for the determination of Ag(I). The g-C 3 N 4 -PtNPs hybrid was synthesized by reduction of chloroplatinic acid using sodium borohydride under ultrasonication and in the presence of g-C 3 N 4 . The hybrid can catalyze the oxidation 3,3′,5,5′-tetramethylbenzidine (TMB) to produce a blue-colored product with an absorption maximum at 652 nm. On addition of Ag(I) and in the presence of citric acid, it will be reduced to form Ag(0) under the catalytic action of PtNPs. Ag(0) is then adsorbed on the surface of the g-C 3 N 4 -PtNPs. This results in the inhibition of the enzyme mimetic activity of the hybrid. Hence, less blue product will be formed from TMB. Under optimum conditions, Ag(I) can be quantified in the 0.05–5.0 nM concentration range with a 22 pM detection limit. This assay is rapid and reliable and was applied to the determination of Ag(I) in spiked real water samples.
A hybrid nanomaterial consisting of graphitic carbon nitride and platinum nanoparticles (g-C 3 N 4 -PtNPs) can catalyze the oxidation of tetramethylbenzidine (TMB) to produce a blue-colored product (TMBox). The enzyme mimetic activity of the hybrid is inhibited by Ag + , thereby decreasing the generation of blue product from TMB.
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COMPOSITES PART B-ENGINEERING
·
2024
·
IF 12.7
Lijiaqi Zhang,Yong Huang,Min Wu
Due to the excellent properties of nanocellulose film such as biodegradability and renewability, researchers have conducted in-depth research on it in recent years. However, rich hydroxyl groups on the surface of nanocellulose make it hydrophilic , and small gaps between the fibrils have significant capillary effect, which cause the strength of nanocellulose film drastically deteriorates when exposed to water, severely restricting its scope of use. In this study, the nanocellulose prepared by ball milling was used to prepare nanocellulose film, and the surface of the film was partially dissolved by ZnCl 2 . The dense regenerated cellulose (Cellulose Ⅱ) with Zn 2+ on the surface made the film hydrophobic, effectively reduced the water absorption rate of the film, and also maintained the internal structure of the nanocellulose. Through this strategy, the nanocellulose film with high dry strength (151–176 MPa), wet strength (27.6–31.7 MPa), high light transmittance (80–91%), and adjustable haze (50–90%) was obtained. This study provides a facile and environmentally friendly strategy to improve the wet strength of nanocellulose film, which broadens its application prospect in packaging materials and electronic devices.
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RSC Advances
·
2016
·Vol. 6
·期 59
·54020-54026
·
IF 3.289
Jikuan Qiu,Yuling Zhao,Huiyong Wang,Guokai Cui,Jianji Wang
Development of new efficient catalytic systems for chemical transformation of CO2 is a very attractive topic in green chemistry. In this work, we studied the synthesis of α-alkylidene cyclic carbonates through the coupling reaction between propargylic alcohols and CO2 with new silver catalysts. It was found that activated carbon supported AgX (X = Br and I) was a simple and efficient catalyst for the carboxylative cyclization of propargyl alcohols with CO2 at atmospheric pressure and room temperature. Nearly 99% yield of the desired product was obtained, and the product could be simply separated through solvent extraction. Moreover, the catalyst could be easily recovered and reused at least ten times without a decrease in the catalytic activity and selectivity. These findings are useful for the development of an environmentally friendly chemical process for the production of α-alkylidene cyclic carbonates.
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