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NEW JOURNAL OF CHEMISTRY · 2021 ·Vol. 45 ·期 37 ·17544-17550 · IF 3.591

From BaCl2 to Ba(NO3)Cl: significantly enhanced birefringence derived from π-conjugated [NO3]

Zhen Chen,Hao Zeng,Shujuan Han,Zhihua Yang,Shilie Pan

The chlorine barium nitrate Ba(NO3)Cl was synthesized, for the first time to the best of our knowledge, by using a mild hydrothermal method. Its structure was observed to feature an ABW-type topology (BaCl-ABW) framework, which can be considered as stacks of honeycomb-shaped sheets. Also, Ba(NO3)Cl crystals with dimensions of up to 2 × 1 × 0.5 mm3 were grown. Remarkably, Ba(NO3)Cl was found to exhibit a short UV cutoff edge (below 213 nm) and a markedly enhanced birefringence (Δn = 0.178 @ 1064 nm), about 19 times that of its parent phase BaCl2 (Δn = 0.009 @ 1064 nm). Theoretical calculations indicated that the birefringence enhancement mainly derived from the planar [NO3] triangles.

CAS / MDL: 10025-91-9 10022-31-8
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Small · 2021 ·Vol. 17 ·期 28 ·2101403 · IF 13.281

CsPbX3-ITO (X = Cl, Br, I) Nano-Heterojunctions: Voltage Tuned Positive to Negative Photoresponse

Qiqian He,Gaoyu Chen,Yongkai Wang,Xiaoyu Liu,Danting Xu,Xiangxing Xu,Ying Liu,Jianchun Bao,Xun Wang

All-Inorganic perovskite CsPbX 3 (X = Cl, Br, I) quantum dots (QDs) have attracted tremendous attention in the past few years for their appealing performance in optoelectronic applications. Major properties of CsPbX 3 QDs include the positive photoconductivity (PPC) and the defect tolerance of the in-band trap states. Here it is reported that when hybridizing CsPbX 3 QDs with indium tin oxide (ITO) nanocrystals to form CsPbX 3 -ITO nano-heterojunctions (NHJs), a voltage tuned photoresponse—from PPC to negative photoconductivity (NPC) transform—is achieved in lateral drain-source structured ITO/CsPbX 3 -ITO-NHJs/ITO devices. A model combining exciton, charge separation, transport, and most critical the voltage driven electron filling of the in-band trap states with drain–source voltage ( V DS ) above a threshold, is proposed to understand this unusual PPC-NPC transform mechanism, which is different from that of any known nanomaterial system. This finding exhibits potentials for developing devices such as photodetectors, optoelectronic switches, and memories.

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CRYSTENGCOMM · 2021 ·Vol. 23 ·期 29 ·5116-5123 · IF 3.545

Cl−-Induced selective fabrication of 3D AgCl microcrystals by a one-pot synthesis method

Jiye Wang,Yazhou Qin,Qiaocui Shi,Luhong Wen,Lei Bi

The controllable preparation of crystals is a prerequisite for exploring their shape-dependent physicochemical properties. Herein, AgCl crystals with different morphologies including octahedron, trapezohedron (TPH), 12-pod and hexapods with mace pods were successfully prepared by a one-pot synthesis method. In the preparation process, ethylene glycol (EG) was used as a solvent and AgNO3 was used as a precursor of Ag+. In particular, the ionic liquid poly(diallyldimethylammonium chloride) (PDDA) not only acted as a Cl− ion precursor but also as a morphology-controlled stabilizer. We further explored the effects of temperature, ligand and precursor concentration on AgCl crystal growth. Moreover, we investigated the effect of Cl− concentration on the morphology of AgCl by adding different amounts of NaCl. We found that under the condition of the lower concentrations of Cl−, {111}-bound octahedral AgCl crystals will transform into TPH enclosed with the {311} facet as the concentration of Cl− ions increases. However, at medium concentrations of Cl−, {111}-bound octahedral AgCl crystals will transform into 3D 12-pod AgCl crystals as the concentration of Cl− ions increases. Under the condition of higher concentrations of Cl−, {111}-bound octahedral AgCl crystals will transform into hexapods with mace pods AgCl crystals as the concentration of Cl− ions increases. According to the experimental results, we proposed the growth mechanism of AgCl microcrystals. This work not only provides a new method for the synthesis of AgCl crystals with a tunable shape, but also helps to understand the crystal growth mechanism.

CAS / MDL: 26062-79-3
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JOURNAL OF LUMINESCENCE · 2020 · IF 3.28

Pyrene Derived aggregation-induced emission sensor for highly selective detection of explosive CL-20

Cheng Zhang,Xihao Pan,Siyao Cheng,Aming Xie,Wei Dong

With the increasingly severe international situation, explosive detection has become an important topic of national security, and the rapid and efficient chemical sensors have attracted people's attention. In this work, a novel sensor CSA was synthesized through cholesterol succinate and 1-Aminopyrene. UV–vis and fluorescence spectra showed that CSA had a typical aggregation-induced emission (AIE) effect in THF/H 2 O solution, and explosive CL-20 could effectively quench this fluorescence. Also, the seal and cotton swab prepared by CSA can specifically detect CL-20, providing a platform for the practical application of CSA in public safety.

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DALTON TRANSACTIONS · 2020 ·Vol. 49 ·期 15 ·4914-4919 · IF 4.174

BaLiTe2O5X (X = Cl, Br): mixed alkali/alkaline-earth metal tellurite halides with [Te2O5]∞ chains

Ting Wang,Yi-Gang Chen,Yao Guo,Fang Wang,Qi Song,Ying-Jie Jia,Xian-Ming Zhang

Isostructural mixed alkali/alkaline-earth metal tellurite halides BaLiTe2O5X (X = Cl, Br) have been successfully synthesized by a mild hydrothermal method, which possess the [Te2O5]∞ chains formed by the corner-sharing connections of the TeO3 and TeO4 polyhedra. The [Te2O5]∞ chains are bridged via the LiO3 polyhedra to form the [LiTe2O5]∞ layers with 4- and 6-membered rings. The adjacent [LiTe2O5]∞ layers are linked via the BaO9 polyhedra to form the [BaLiTe2O5]∞ double layers, which are further connected via weak Ba–X–Li interactions to generate a 3D framework. Analysis of different lithium tellurites shows that the different arrangements of the Te–O and Li–O units in the lithium tellurites can be attributed to the cation–cation repulsion and lone-pair effect. Both compounds display good thermal stability, wide optical bandgaps (4.25 and 4.13 eV), and large birefringence. First-principles calculations indicate that the TeOn groups and X− determine the optical properties of BaLiTe2O5X (X = Cl, Br).

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POLYMERS FOR ADVANCED TECHNOLOGIES · 2019 ·Vol. 31 ·期 5 ·1059-1066 · IF 2.162

Synthesis and properties of shape memory polymers of LLA, TMC, and ε-CL terpolymers

Shaohua Wen,Yongfei Li

Biodegradable polylactide (PLA) and its copolymers with shape memory properties have attracted great interests because of their important application prospects in biomedical field. In this study, random poly(L-lactide-co-trimethylene carbonate-co-ε-caprolactone) (LTCL) terpolymers with different molar ratio were synthesized and characterized. Monomer ε-caprolactone (ε-CL) was used in this study instead of glycolide in preliminary study of LTG terpolymers to investigate the transition temperature and the shape memory performance. Characterization on crystallization, mechanical properties, shape fixing, and recovery ratios of the terpolymers was conducted to investigate the correlation between crystallization and shape memory performance of LTCL terpolymers. The results are consistent with the formation of crystallized LLA segments, which could act as crosslinks, strengthened the stationary phase within the polymer matrix, and significantly improved the shape memory performance of LTCL terpolymers. For example, LTCL801010 is a crystalline polymer with high shape fixity and shape recovery ratio; its shape recovery temperature is 39°C. LTCL terpolymers with high CL content do not show shape memory performance for the rubbery at room temperature. Based on this study, PLA materials with shape memory property can be designed through the selection of monomers or the adjustment of comonomer ratio. These polymers with recovery temperature close to 37°C are expected to be used in human body such as scaffolds in tissue engineering.

CAS / MDL: 502-44-3 17501-44-9
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DIAMOND AND RELATED MATERIALS · 2023 · IF 4.1

Design and preparation of a novel nano-composite coating for desensitization of CL-20

Peng Bao,Yaning Li,Wei Xiao,Wenxiang Bian,Jian Li,Mingshuai Xue,Saichao Song,Boliang Wang

Although 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20) is one of the best high-energy explosives, its application is severely limited by its high sensitivity. Herein, a composite wax-film with interfacial crosslinking anti-falling was designed and fabricated to desensitize CL-20. It was filled with nano-silica powder (n-Si), nano-graphenes (n-GPNs) and multi-walled carbon nanotubes (MWCNTs) as insensitive enhancers. A unique and stable core-shell composite explosive was prepared, and characterized by DSC , SEM, TEM, XRD , XPS as well as mechanical sensitivity tests. The results suggested that the functional group interaction and structural strengthening between enhancers and microcrystalline wax (MW) further enhanced the desensitization ability of the composite film for CL-20. Because of the hydrogen bonding and thickening enhancement, the CL-20 crystal was uniformly coated with a nano-composite film. Three enhancers were demonstrated to be highly compatible with CL-20. In comparison with MW@CL-20, The E a , T p0 and T b of the composites containing n-GPNs increased by >375.27 kJ·mol −1 , 21.04 °C and 18.27 °C, respectively. The SEM and XPS results showed that the composite performed a complete core-shell structure with thermal softening resistance and superior coverage (98.20 %). The insensitive enhancer was also distributed and embedded in the MW-film matrix. Besides, the anti-fall and cross-linking properties of the film enable the mechanical sensitivity of the composite explosive to reach to a level better than that of WO 3 /Al nanothermite with 5 wt% polyaniline and polymer-bonded explosive (PBX) with 95 wt% LLM-105 and 5 wt% ternary composite. The heterogeneous composites demonstrated excellent mechanical safety and high energy performance. These findings can provide a reference for the efficient desensitization of CL-20.

CAS / MDL: 308068-56-6
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ACS Applied Materials & Interfaces · 2023 · IF 9.5

High Thermoelectric Performance in Cu-Doped Bi2Te2.7Se0.33 Due to Cl Doping and Multiscale AgBiSe2

Abubakar Yakubu Haruna,Yubo Luo,Zheng Ma,Wang Li,Haiqiang Liu,Xin Li,Qinghui Jiang,Junyou Yang

The thermoelectric performance of n-type Bi2Te3 needs further enhancement to match that of its p-type Bi2Te3 counterpart and should be considered for competitive applications. Combining Cu/Cl and multiscale additives (AgBiSe2) presents a suitable route for such enhancement. This is evidence of the enhanced thermoelectric performance of Bi1.995Cu0.005Te2.69Se0.33Cl0.03. Moreover, by incorporating 0.65 wt % AgBiSe2 (ABS) into Bi1.995Cu0.005Te2.69Se0.33Cl0.03, we further reduce its lattice thermal conductivity to ∼0.28 W m–1 K–1 at 353 K owing to the extra phonon scattering of multiscale ABS. Additionally, the Seebeck coefficient enhances (−183.89 μV K–1 at 353 K) owing to the matrix’s reduced carrier concentration caused by ABS. As a result, we achieve a high ZT of ∼1.25 (at 353 K) and a high ZTave of ∼1.12 at 300–433 K for Bi1.995Cu0.005Te2.69Se0.33Cl0.03 + 0.65 wt % ABS. This work provides a promising strategy for enhancing the thermoelectric performance of n-type Bi2Te3 through Cu/Cl doping and ABS incorporation.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Improving electrochemical properties of Li4Ti5O12/TiO2 diphase anode materials via Co-Cl co-doping

Lingyao Zou,Lu Gan,Wenli Song,Chunying Rong,Lishan Yang,Liping Yu,Zhongyun Ma,Shixun Lian

The rapid development of highly durable electric vehicles has put forward higher requirements for lithium-ion batteries. Li 4 Ti 5 O 12 (LTO) is widely studied owing to its long service life and safety. However, owing to their low electrical conductivity and diffusion, lithium ions have limited practical applications. In this study, Co-Cl co-doped LTO/TiO 2 diphase (LTOT) nanosheets were prepared via the hydrothermal method . The synergistic effect of Co-Cl co-doping reduced the charge-transfer resistance of LTOT and increased the lithium-ion diffusion coefficient , thereby improving the dynamic behavior of the electrode material, which further enhances the rate capability and cycle performance of LTOT. The optimized LTOT:Co-Cl composite exhibited excellent cycle performance and rate capability (the ninth cycle reversible capacities were 253.8, 222.2, 200.1, 185.7, 169.9, 161.3, and 146.3 mAh·g −1 at the current density of 1, 2, 5, 10, 20, 30, and 50 C (1 C = 175 mA·g −1 ) rate, respectively). In addition, LTOT:Co-Cl maintained a capacity of 120 mAh·g −1 after 5000 cycles at 50 C with a retention rate of 83 %, indicating that the average decay rate per cycle is only 0.003 % during the long charge/discharge process.

CAS / MDL: 5593-70-4 9022-96-2
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Frontiers in Chemistry · 2023 · IF 5.5

Preparation of CsPb(Cl/Br)3/TiO2:Eu3+ composites for white light emitting diodes

Zhang Chen,Wang Minqiang,Shi Jindou,Wang Junnan,Da Zheyuan,Zhou Yun,Xu Youlong,Gaponenko Nikolai V.,Bhatti Arshad Saleem

The inherent single narrow emission peak and fast anion exchange process of cesium lead halide perovskite CsPbX3 (X = Cl, Br, I) nanocrystals severely limited its application in white light-emitting diodes. Previous studies have shown that composite structures can passivate surface defects of NCs and improve the stability of perovskite materials, but complex post-treatment processes commonly lead to dissolution of NCs. In this study, CsPb(Cl/Br)3 NCs was in-situ grown in TiO2 hollow shells doped with Eu3+ ions by a modified thermal injection method to prepare CsPb(Cl/Br)3/TiO2:Eu3+ composites with direct excitation of white light without additional treatment. Among them, the well-crystalline TiO2 shells acted as both a substrate for the dopant, avoiding the direct doping of Eu3+ into the interior of NCs to affect the crystal structure of the perovskite materials, and also as a protection layer to isolate the contact between PL quenching molecules and NCs, which significantly improves the stability. Further, the WLED prepared using the composites had bright white light emission, luminous efficiency of 87.39 lm/W, and long-time operating stability, which provided new options for the development of perovskite devices.

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ACS Applied Materials & Interfaces · 2019 · IF 8.456

Grinding Synthesis of APbX3 (A = MA, FA, Cs; X = Cl, Br, I) Perovskite Nanocrystals

Daqin Chen,Junni Li,Xiao Chen,Jiangkun Chen,Jiasong Zhong

Currently, metal halide perovskite nanocrystals have been extensively explored due to their unique optoelectronic properties and wide application prospects. In the present work, a facile grinding method is developed to prepare whole-family APbX3 (A = MA, FA, and Cs; X = Cl, Br, and I) perovskite nanocrystals. This strategy alleviates the harsh synthesis conditions of precursor dissolution, atmosphere protection, and high temperature. Impressively, the as-prepared perovskite nanocrystals are evidenced to have halogen-rich surfaces and yield visible full-spectral emissions with maximal photoluminescence quantum yield up to 92% and excellent stability. Additionally, the grinding method can be extended to synthesize widely concerned Mn2+-doped CsPbCl3 nanocrystals with dual-modal emissions of both excitons and dopants. As a proof-of-concept experiment, the present perovskite nanocrystals are demonstrated to be applicable as blue/green/red color converters in UV-excitable white-light-emitting diodes.

CAS / MDL: 7758-95-4
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

MOF-derived Cl/O-doped C/CoO and C nanoparticles for high performance supercapacitor

Ji Ying Long,Zhi Shuo Yan,Yun Gong,Jian Hua Lin

Based on a meta-organic framework (MOF) formulated as [Co 4 (phen) 4 Cl 8 ] (phen = 1, 10-phenanthroline) as precursor, Cl/O doped C/CoO material (C/CoO-200) was synthesized by a one-step calcining method at a low temperature of 200 °C. In C/CoO-200, CoO nanoparticles with an average size of 25 nm were linked by carbon matrix into particles with the diameter of 200 nm ∼ 1 μm. The sample possessed a very low atomic percentage of CoO (CoO: 1.9%; C: 86.8%) due to the large amount of carbon from the organic ligand, phen in the precursor. However, it still exhibited a large specific capacitance of 1052 F g −1 at 0.5 A g −1 in 2 M KOH electrolyte with a 79.6% capacitance retention at 10 A g −1 . After successive etched in acid, Cl/O doped carbon nanoparticles were obtained. C-300 was composed by individual nanoparticles with size of 100–500 nm, it showed a specific capacitance of 207 and 164 F g −1 in 2 M KOH at a current density of 0.5 and 1 A g −1 , respectively, which was comparable to the commercial activated carbon (AC) (199 and 179 F g −1 for AC at 0.5 and 1 A g −1 , respectively). An asymmetric supercapacitor based on the positive electrode of C/CoO-200 and the negative electrode of C-300 exhibited a stable performance with a 61% retention of specific capacitance after 10,000 charging-discharging cycles at 1.5 A g −1 .

CAS / MDL: 25249-54-1 9003-39-8
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