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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2020 · IF 4.495

A promising optical limiting material: Tunable third-order nonlinear optical properties of robust CsPbX3 (X=Cl/Br, Br) nanocrystals glasses

Mengfeifei Jin,Xiaojuan Liang,Huiling Zhang,Jianming Liu,Guangzhan Shao,Weidong Xiang,Yinglin Song

As laser technology advances, the importance of laser protection puts an urgent demand for robust and high-efficient optical limiting materials. In this work, CsPbX 3 (X = Cl/Br, Br) NCs were synthesized by precisely controlling the ratio of Cl − to Br − and the heat treatment temperature, and the third-order nonlinear (TONL) optical properties of them were investigated systematically and deeply based on a nonlinear optical imaging technique with the phase-object (NIT-PO) at 532 nm for the first time. All of them demonstrate strong reverse saturation absorption (∼10 -12 –10 -11 m/W), and the sign of TONL refraction index (γ) relates to the component (CsPb(Cl/Br) 3 NCs glasses: ∼10 -20 m 2 /W, CsPbBr 3 NCs glasses: ∼−10 -20 to 10 -19 m 2 /W). In addition, they have excellent characteristics of thermal stability and water stability, as well as photostability under 455 nm laser irradiation, indicating that it is a promising optical limiting material.

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ACS Applied Nano Materials · 2024 · IF 5.3

Ag/AgX (X = Cl, Br, or I) Nanocomposite Loaded on Ag3PO4 Tetrapods as a Photocatalyst for the Degradation of Contaminants

Yu Yao,Qianhong Shen,Qifeng Chen,Yanyan He,Libei Jiang,Jie Liu,Yue Li,Xudan Cao,Hui Yang

A silver phosphate (Ag3PO4)/silver (Ag)/silver halide (AgX, X = Cl, Br, or I) ternary composite photocatalysts were prepared by loading Ag nanoparticles on Ag3PO4 tetrapods followed with in situ halogenation. The interface charge transfer behavior in the Ag3PO4/Ag/AgX nanocomposite was studied, and the photocatalytic performance was also evaluated. The results show that the Ag3PO4/Ag/AgI photocatalyst exhibits higher photocatalytic activity than the other two photocatalysts due to the more matched band structure between AgI and Ag3PO4. An internal electric field (IEF) from Ag3PO4 to AgI is formed at the heterogeneous interface, so the photogenerated electrons at the conduction band of AgI can rapidly transfer to the valence band of Ag3PO4 and recombine with photogenerated holes, which is consistent with the S-scheme charge transfer mechanism. Meanwhile, the photogenerated electrons left at the conduction band of Ag3PO4 can transfer to Ag nanoparticles due to the Schottky junction and react with oxygen to produce •O2–, which is proved to be the main active species in the photocatalytic procedure. This tandem junction modulated between the S-scheme heterojunction and Schottky junction promotes the efficient separation of photogenerated carriers, thus significantly increasing the average PL lifetime of electrons by 2.95 times. Therefore, the Ag3PO4/Ag/AgI photocatalyst exhibits excellent photocatalytic activity for the degradation of methylene blue and norfloxacin. The seven consecutive cyclic tests prove the good stability of the photocatalyst, thus showing the application potential in the field of sewage treatment.

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CHINESE JOURNAL OF CATALYSIS · 2016 · IF 2.628

C–X (X = Cl, Br, I) bond dissociation energy as a descriptor for the redispersion of sintered Au/AC catalysts

Xinping Duan,Yan Yin,Xuelin Tian,Jinhuo Ke,Zhaojun Wen,Jianwei Zheng,Menglin Hu,Linmin Ye,Youzhu Yuan

Disintegration or redispersion of supported sintered gold nanoparticles (Au NPs) in the presence of alkyl halide can give catalyst regeneration or redispersion of sintered Au catalysts. The selectivity of alkyl halides, temperature and size distributions were investigated to elucidate the redispersion of Au NPs during halide-induced decomposition. This study proved that the alkyl halide induced the redispersion of sintered Au NPs which depended on the R–X (X = I, Br, Cl) bond dissociation energy (BDE) and thus provided a simple descriptor for the regeneration of inactive supported Au catalysts. A correlation between the BDE of R–X and dispersion efficiency was established. The tendency for disintegration and redispersion followed the R–X BDE of the alkyl halide. Compared to alkyl chlorides and bromides, iodides were more efficient for redispersing sintered Au NPs. As a descriptor, the BDE of R–I played a crucial role in particle redispersion. These findings provided insights into the mechanism of organic halide-induced Au NP disintegration and the effect of the halide type on the redispersion of sintered catalysts.

CAS / MDL: 16961-25-4
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2024 ·Vol. 171 ·期 11 ·111502 · IF 3.1

Experimental and Computational Insights into the Effects of -NH2 and -Cl Functional Groups on the Copper Corrosion Inhibition by Benzotriazole

Thanh Hai Pham,Viorel Chihaia,Phung K. Le,Do Ngoc Son

The influences of -NH2 and -Cl groups on the copper corrosion inhibition in 0.5 M H2SO4 solution by benzotriazole were studied using experimental methods and density functional theory calculations. Mass loss tests, potentiodynamic polarization, and surface morphology analyses revealed notable differences: while unmodified benzotriazole showed an inhibition efficiency of 76.6%, the -Cl derivative increased this to 87.6%, whereas the -NH2 derivative dropped it to 61.0% at the concentration of 5 × 10−4 M. Density functional theory calculations indicated these differences are not due to electronic properties or inhibitor-copper interaction energies but rather to the inhibitor's influence on the oxygen reduction reaction, especially O2 and H2O adsorption. The -NH2 group formed strong hydrogen bonds with O2 and H2O, reducing oxygen reduction inhibition, while the -Cl group repelled O2, resulting in enhanced inhibition. Free energy analysis of the oxygen reduction reaction supported these findings. These new insights into benzotriazole derivatives' copper corrosion inhibition mechanisms offer valuable guidance for developing next-generation corrosion inhibitors.

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INORGANIC CHEMISTRY COMMUNICATIONS · 2024 · IF 4.4

Facile preparation of nickel-iron bimetallic oxides doped with g-C3N4 and influence on thermal decomposition of hexanitrohexaazaisowurtzitane (CL-20)

Tengyue Song,Yuhuai Shi,Xueli Zhang,Wenhui Wang,Wenkuang Pan,Guangwei Xiao,Mengli Yin,Xiong Cao

Energetic solid propellants are critical technologies for advancing strategic and tactical weaponry. To further develop the application of CL-20 to energetic solid propellants, it is necessary to explore more efficient catalysts to enhance their thermal decomposition characteristics. In this paper, three composites of nickel–iron layered double oxides doped with 0 wt%, 5 wt% and 20 wt% g-C 3 N 4 (NiFe-LDO/g-C 3 N 4 ) were synthesized by co-precipitation and heat treatment methods. These composites were characterized using Scanning electron microscope (SEM), X-Ray diffractometer (XRD), Fourier transform infrared (FT-IR) spectrometer, and X-ray photoelectron spectrometer (XPS). Three prepared composites were tested for catalytic pyrolysis performance of CL-20 using Differential scanning calorimeter (DSC). The results show that NiFe-LDO/g-C 3 N 4 has an excellent layered structure and can significantly enhance the thermal decomposition performance of CL-20. Compared with 253.52 °C for raw CL-20, the thermal decomposition peak temperatures decreased to 246.61 °C, 245.64 °C and 244.08 °C after addition of the three catalysts, respectively. Additionally, the activation energies declined from 234.02 kJ·mol −1 to 192.55 kJ·mol −1 , 176.33 kJ·mol −1 and 160.78 kJ·mol −1 . Then, a potential catalytic mechanism is proposed. This study shows that NiFe-LDO/g-C 3 N 4 serves as a high-quality catalyst for the enhancement of CL-20 thermal decomposition performance, with further prospective applications in solid propellants.

CAS / MDL: 108-78-1 7791-20-0
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MICROCHEMICAL JOURNAL · 2024 · IF 4.9

Dual emissive Cl, N-codoped carbon dots for highly selective and sensitive detection of amphotericin B in milk and wastewater

Guang-Ming Bao,Shun-Qiang Cui,Yi-Fan Xia,Zhen-Chong Dou,Xia Wei,Zhi-Qiang Cai,Peiyao Chen,Yi Zhang,Yu-Xin Chen,Hou-Qun Yuan

Amphotericin B (AmB) is an antifungal drug used in dairy farming. It is significant to monitor AmB in milk and environmental water as AmB is severely toxic. Herein, dual emissive Cl, N-codoped carbon dots (Cl, N-CDs) were facilely synthesized and explored as fluorescent probes for specific recognition of AmB among sixty-eight common substances. The Cl, N-CDs possess long emission wavelengths (650 and 482 nm), large stokes shift (240 nm), and high quantum yield (22.06 %). The fluorescence of Cl, N-CDs can be specifically quenched by AmB with a linear concentration range of 0.1–6 μM, a detection limit of 6.67 nM, and a response time within 1 min. Moreover, the Cl, N-CDs can be applied for the determination of AmB in milk and wastewater with good recoveries (92.00–110.00 %). This work provides a facile method for the preparation of Cl, N-codoped CDs with excellent fluorescence properties, and develops a new approach for fluorescence quantification of AmB in real samples.

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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Design a cross-linked film based on cellulose nanocrystals doping for enhancing the interfacial performance and desensitization of CL-20

Peng Bao,Su Jiang,Yang Chen,Yuanlin Fan,Yaning Li,Boliang Wang

Despite the extensive researches on CL-20 crystals, the mechanical safety issues and process problems of CL-20 applications have not been studied in-depth. Herein, the cellulose nanocrystals (CNC) was doped in microcrystalline wax (MW), oxidized microcrystalline wax (OMW) and hydrogel (PPC) to design and fabricate the cross-linked CL-20 composites by simple water-suspension melting and freeze-drying methods. The composites were characterized by SEM, XPS, TG-DSC, XRD, mechanical sensitivity device and inclined chute tester. It is found that the CNC@OMW composite film exhibits excellent coating effect (99.96%) on CL-20 due to the cross-linking results. The E a of CL-20 is increased from 190.92 to 388.71 kJ/mol under the synergistic effect of the excellent compatibility between components and the compact coating structure of CNC@OMW. Additionally, the film enhances the T p0 of CL-20 from 218.15 to 222.66 ℃ and T b from 220.27 to 223.73 ℃, respectively. While, the PPC@CNC only promoted E a , T p0 and T b of CL-20–292.89.71 kJ/mol, 224.22 ℃ and 225.66 ℃, respectively. Besides, the XRD results confirms that three composite films dose not cause a transformation of the ε- CL-20 crystal phase. Most importantly, the cross-linked film brings mechanical sensitivity of CL-20 from 60 N and 3.5 J to a level of over 360 N and 10.4 J, comparable to WO 3 /Al nanothermite with 5 wt% polyaniline (360 N) and composite with 95 wt% LLM-105 and 5 wt% ternary (11–12 J). This improvement enables the composite explosives to be handled using standard procedures. Furthermore, the ability of the particles to accumulate electrostatic charge after cross-linking coating is significantly reduced, and PVC is more suitable as the contact material of CL-20 and composite particles than copper for use in the transportation and packaging. These findings can serve as a reference for wide application of CL-20.

CAS / MDL: 5323-95-5
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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2025 · IF 2.1

Phase Equilibria and Phase Diagram of the Quaternary System (Na+, K+, Ca2+//Cl– -H2O) and Its Subsystems at 338.15 K

Ruxue Yao,Yang Ge,Jiangtao Song,Fei Yuan,Yafei Guo,Tianlong Deng

The Qaidam Basin has potassium- and calcium-rich oil field brine resources at high temperatures. Since the phase diagram is a powerful tool to guide the separation and purification of inorganic chemical engineering for the development of potassium resources in oil field brine, the quaternary oil field brine system (Na+, K+, Ca2+//Cl– -H2O) and its two subsystems ((Na+, Ca2+//Cl– -H2O) and (K+, Ca2+, //Cl– -H2O)) at 338.15 K were reported for the first time by the isothermal dissolution equilibrium method. The compositions of the equilibrium solid phases were analyzed and identified by combined chemical analyzing and X-ray diffraction. The quaternary system has four crystallized regions corresponding to NaCl, KCl, KCl·CaCl2, and CaCl2·2H2O at 338.15 K, and the incongruent double salt KCl·CaCl2 occurred at 338.15 K. The study facilitates the enrichment of thermodynamic data and exploits brine-based potassium resources.

CAS / MDL: 7647-14-5 7447-40-7
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Preparation of microstructure controllable CL-20/FOX-7 composite microspheres by microchannel recrystallization technology to enhance safety and combustion performance

Wenqing Li,Shimin Zhang,Songchao Shi,Xiaoying Cheng,Chongwei An,Jingyu Wang,Baoyun Ye

Realizing the balance between high energy density and multifunctionality of energetic materials is a hot spot in current research, and its study is of great significance for the application of energetic materials. Regulating microstructure is widely recognized as an effective strategy for solving such problems. In this paper, four different microstructures of Hexanitrohexaazaisowurtzitane(CL-20)/1,1-diamino-2,2-dinitroethylene(FOX-7) composite microspheres, namely, hollow, porous irregular microspheres, porous microspheres, and layered porous microspheres, were prepared by microchannel recrystallization technology. The effects of crystal precipitation rate, binder mechanical properties, and purity of water phase on the microstructure of composite microspheres were systematically investigated. The four prepared samples were spherical particles with regular morphology and uniform particle size. The angle of repose and mechanical sensitivity tests showed that the CL-20/FOX-7 composite microspheres had good dispersibility and mechanical sensitivity. Ignition experiments show that hollow microspheres have the best energy release efficiency, while porous microspheres have higher energy density and more stable energy release efficiency. The results show that the combustion performance and safety of the composite microspheres can be effectively enhanced by adjusting the microstructure. Microchannel recrystallization technology can realize the controllable preparation of the microstructure of composite microspheres, which provides a reference for the design and preparation of other composite microspheres.

CAS / MDL: 9002-89-5
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POWDER TECHNOLOGY · 2025 · IF 4.6

Preparation of microstructure controlled spherical co-aggregated composite energetic materials: Synergistic enhancement of safety and thermal stability of CL-20

Wenyu Wu,Wenjie Liu,Meijie Li,Penglin Kang,Dongqian Fan,Xiaodong Li,Shuangqi Hu

Regulating the structure of energetic materials to enhance safety performance has become a hot topic for researchers in recent years. This study prepared spherical co-aggregated CL-20/HMX with controllable microstructure using a combination of microfluidic and self-assembly strategies within a modular micro-reaction system. The morphology and agglomeration structures of CL-20/HMX particles were investigated with different mixing plates, solvent/nonsolvent flow rate ratio, and solvent content. Spherical co-aggregated CL-20/HMX co-crystals were prepared under optimized conditions, and the formation mechanism was analyzed. The impact of the spherical aggregation structure on the thermal properties and mechanical sensitivity was thoroughly studied. The results indicate that the spherical co-aggregated CL-20/HMX was assembled from lamellar nanoparticles, controlling CL-20 crystal morphology at the molecular level. CL-20/HMX co-aggregated microspheres exhibit higher mechanical safety and thermal stability than conventional reaction samples and physical mixing samples. Combining spherical aggregation structures and a microfluidic approach enhances thermal decomposition stability and improves safety. This research offers a novel strategy for developing and fabricating other energetic materials.

CAS / MDL: 67-68-5
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Analytical Methods · 2016 ·Vol. 8 ·期 44 ·7929-7936 · IF 1.915

A chemiluminescent aptasensor for simultaneous detection of three antibiotics in milk

Liling Hao,Huajie Gu,Nuo Duan,Shijia Wu,Zhouping Wang

In this study, a highly sensitive and specific multiplex chemiluminescent method for the simultaneous detection of three antibiotics was fabricated. Thiolated hybridized complementary strand (cDNA) modified N-(4-aminobutyl)-N-ethylisoluminol (ABEI) functionalized flowerlike gold nanostructures (AuNFs) were used as signal probes. Oxytetracycline (OTC), tetracycline (TET) and kanamycin (Kana) aptamers that were fixed onto the bottom of microtiter plates were used as recognition molecules. Targets and signal probes can competitively combine with the fixed aptamers. Thus, OTC, TET and Kana can be simultaneously detected based on an ABEI–H2O2–P-iodophenol (PIP) steady-state chemiluminescence (CL) system and the CL intensity is related to the negative logarithm of the concentrations of OTC/TET/Kana, respectively. The ranges are 0.05 to 5 ng mL−1, 0.05 to 5 ng mL−1, and 0.005 to 0.5 ng mL−1, and the detection limits are 0.02, 0.02 and 0.002 ng mL−1 (S/N = 3), respectively. The capability of the bioassay in milk was also studied using the standard addition recovery method, and the results showed a good consistency with the ones that were obtained from a commercial ELISA method. Owing to the advantages of a simple operation procedure, and excellent selectivity and specificity, the proposed biosensor demonstrated great potential in the application of food safety and multiplex nanosensors.

研究领域: 分析化学 · 食品安全 · 纳米技术 · 生物传感器
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Nature Communications · 2025 ·Vol. 16 ·期 1 ·1-11 · IF 15.7

Engineered PW12-polyoxometalate docked Fe sites on CoFe hydroxide anode for durable seawater electrolysis

He Xun,Yao Yongchao,Zhang Min,Zhou Yilei,Zhang Limei,Ren Yuchun,Dong Kai,Tang Hong,Nan Jue,Zhou Xingli,Luo Han,Ying Binwu,Yu Qi,Luo Fengming,Tang Bo,Sun Xuping

Seawater electrolysis driven by offshore renewable energy is a promising avenue for large-scale hydrogen production but faces challenges in designing robust anodes that suppress surface chlorine reactions and corrosion at high current densities. Here we report a strategy by selectively docking PW 12 -polyoxometalate (PW 12 -POM) onto Fe sites of CoFe hydroxide anode to modulate the electronic structure of adjacent Co active centers and regulate Cl⁻/OH⁻ adsorption for efficient alkaline seawater oxidation. Our CoFe-based anode achieves low overpotentials, high catalytic selectivity, and notable durability, with continuous operation at 1 A cm⁻² for over 1300 hours and at 2 A cm⁻² more than 600 hours. Theoretical calculations and ex situ/in situ analyses reveal that PW 12 -POM coordination at Fe sites stabilizes Fe, suppresses its leaching, modulates Co acidity, promotes OH⁻ adsorption, and protects metal sites from Cl⁻ corrosion.

研究领域: 电化学 · 材料科学 · 能量转换 · 催化 · 可再生能源 · 表面化学
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