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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Improved photocatalytic activity of Bi2MoO6 by modifying the halogen ions (Cl−, Br−, or I−) for photoreduction of N2 into NH3

Dekun Shi,Zhaojun Shi,Lixin Zhang,Yaan Cao

A series of halogen ions (Cl − , Br − , or I − ) modified Bi 2 MoO 6 (Bi 2 MoO 6 –Cl, Bi 2 MoO 6 –Br, or Bi 2 MoO 6 –I) are synthesized via a one-step solvothermal method . It is determined that the halogen ions (Cl − , Br − , or I − ) are modified on the surface of Bi 2 MoO 6 as the -Bi-Cl, -Bi-Br, or -Bi-I species (the connected Bi 3+ is coordinated with three lattice O2- ions in Bi 2 MoO 6 ). The -Bi-Cl, -Bi-Br, or -Bi-I species on the Bi 2 MoO 6 surface can act as highly active sites to polarize and activate the N 2 and H 2 O molecules adsorbed on the surface of catalysts. Moreover, due to the surface-modified -Bi-Cl, -Bi-Br, or -Bi-I species, the visible light absorption is improved, the separation of photogenerated charge carriers is promoted, as well the band structure is better matched with the redox potential of photoreduction of N 2 . As a result, the photocatalytic activity of Bi 2 MoO 6 –Cl, Bi 2 MoO 6 –Br, or Bi 2 MoO 6 –I is improved for photoreduction of N 2 into NH 3 compared with Bi 2 MoO 6 . Overall, this work provides new insights into the doping states of halogen ions, the surface-active sites, the band structure, the photocatalytic activity, and the mechanism for photoreduction of N 2 into NH 3 for Bi 2 MoO 6 with modification of halogen ions (Cl − , Br − , or I − ).

CAS / MDL: 64-17-5 10035-06-0
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PROPELLANTS EXPLOSIVES PYROTECHNICS · 2021 ·Vol. 46 ·期 12 ·1837-1843 · IF 1.887

Construction of CL-20 Surface Layer with Different Wetting Properties and its Effect on Slurry Rheological Behavior and Mechanical Sensitivities

Shuyi Duan,Feng Ding,Haitao Sun,Chun Xiao,Shangbin Li,Qing Zhu

To have a deep understanding of the effects of surface wettability on the mechanical sensitivity and rheological characteristics of PBX slurry, CL-20 particles with hydrophilic property was prepared through a polymerization process of dopamine, and CL-20 particles with hydrophobic property were prepared through a condensation polymerization process of hexadecyltrimethoxylsilane. The morphology, surface element content and surface wettability of CL-20 crystals before and after modification were characterized by scanning electronic microscope (SEM), X-ray photoelectron spectroscopy (XPS), and contact angle test. The rheological characteristics of CL-20 based PBX slurry showed that the interaction between explosive particles and binder was changed with different surface wettability of CL-20. The weaker interaction between CL-20@hydrophobic and binder lead to weaker solid-liquid friction, resulted in lower apparent viscosities of CL-20@hydrophobic based PBX slurry at high shear rate. The mechanical sensitivity of wax coated CL-20 with different surface wettability was tested. CL-20@hydrophobic-wax exhibited better mechanical stability compared to CL-20-wax and CL-20@hydrophilic-wax, probably owning to the weaker interaction between CL-20@hydrophobic surface and wax.

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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2021 · IF 8.067

High thermoelectric properties realized in earth abundant Bi2S3 bulk materials via Se and Cl co-doping in solution synthesis process

Jun Guo,Yu-Ke Zhu,Lin Chen,Zi-Yuan Wang,Zhen-Hua Ge,Jing Feng

Bi 2 S 3 -based alloys are considered promising thermoelectric materials due to their large Seebeck coefficient and low lattice thermal conductivity . However, low electrical conductivity usually leads to poor electrical transport properties, which seriously restricts their further application in thermoelectric refrigeration and/or power generation. In this work, Bi 2 S 3 with high electrical transport properties is synthesized hydrothermally via Se and Cl co-doping. The maximum electrical conductivity value of 483 S cm −1 was obtained for the Bi 2 S 2.4 Se 0.4 Cl 0.20 sample at room temperature. The significant improvement of electrical conductivity gives rise to a high average power factor of 411 μW m −1 K −2 during the measuring temperature range and a peak value of 456 μW m −1 K −2 at 673 K. Benefiting from the largely improved electrical transport properties, a superior ZT value of approximately 0.66 and ZT ave . of 0.36 were obtained for Bi 2 S 2.4 Se 0.4 Cl 0.20 , and the theoretically calculated conversion efficiency reached 5.7%. The results indicate that Bi 2 S 3 is a promising candidate for thermoelectric applications at medium temperatures.

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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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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2023 · IF 2.6

Phase Equilibria for the Aqueous Quinary System Li+, Na+, K+, Mg2+//Cl––H2O Saturated with NaCl·2H2O at 258.15 K

Tingting Zhou,Xueli Huang,Baharguli Hadeerbieke,Fangning Yan,Xueying Wang,Qinglong Luo

The phase diagram can guide the comprehensive utilization of salt lake brine, particularly lithium extraction. In this paper, the study on phase equilibria of the quinary system Li+, Na+, K+, Mg2+//Cl––H2O saturated with NaCl·2H2O and its subsystem Li+, Na+, Mg2+//Cl––H2O at 258.15 K were carried out using the isothermal dissolution equilibrium method. Based on the experimental data, equilibrium diagrams for stable phases were plotted. For the equilibrium diagram of the quaternary system Li+, Na+, Mg2+//Cl––H2O at 258.15 K, there are two invariant points, five univariant curves, and four crystallization fields. The quinary system Li+, Na+, K+, Mg2+//Cl––H2O saturated with NaCl·2H2O at 258.15 K contains three invariant points, seven univariant curves, and five crystallization fields. Comparing the phase diagram of the system at 258.15 K to that at 298.15 K reveals that, except KCl, all crystallization zones have decreased, and LiCl·MgCl2·7H2O has the smallest crystallization zone compared to the other salts in the systems. This fundamental research could be valuable for promoting comprehensive utilization of the lithium-containing salt lake brine.

CAS / MDL: 7447-41-8
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CHEMICAL ENGINEERING JOURNAL · 2018 · IF 6.735

Direct white emissive Cl-doped graphene quantum dots-based flexible film as a single luminophore for remote tunable UV-WLEDs

Xiao-Fei Wang,Gui-Gen Wang,Jia-Bing Li,Zheng Liu,You-Xiao Chen,Long-Fei Liu,Jie-Cai Han

Herein we first report new chlorine-doped graphene quantum dots (Cl-GQDs) that can be used in solid-state white-light-emitting diodes (WLEDs). The Cl-GQDs with a mean size of 1.53 nm are obtained by one-step hydrothermal method using β-cyclodextrin and hydrochloric acid as the source materials. The PL emission spectra of the Cl-GQDs show an excitation-wavelength-dependent behavior in the range from 300 to 380 nm excitation. Under UV irradiation, the Cl-GQDs can direct emit white light. Given that they are worth using in light-conversion, Cl-GQDs embedded solid composite film (Cl-ESCF), based on silicon resin as host material, is successfully fabricated by solution-processing approach. The freestanding Cl-ESCF has high transparency and flexibility, excellent photostability and temperature resistance, and retains its optical properties in the solid state. In order to realize its potential, the Cl-ESCF converted remote UV-pumped WLED is demonstrated. The results verify that the Cl-GQDs can be homogeneously dispersed within solid matrix without obvious aggregation so that a uniform and defect-free natural white light can be obtained. In addition, our WLED possesses favorable white-light characters with the CIE of (0.33, 0.34), moderate CCT of 5653 K, and high CRI of 87.6, as well as good color and LED stability. This single-phase rare-earth-free white-luminescent Cl-GQDs may be not only expected to prevent the drawbacks of multicolor phosphors, thereby generating high-quality white emission, but also identified to be a green alternative for conventional emitters.

CAS / MDL: 7585-39-9 7647-01-0
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CHEMISTRY OF MATERIALS · 2018 · IF 9.89

Synergetic Effect of Postsynthetic Water Treatment on the Enhanced Photoluminescence and Stability of CsPbX3 (X = Cl, Br, I) Perovskite Nanocrystals

Ying Liu,Fei Li,Quanlin Liu,Zhiguo Xia

All inorganic cesium lead halide CsPbX3 (X = Cl, Br, I) perovskite nanocrystals (NCs) are generally considered to be sensitive and even decompose when exposed to ambient humidity. Herein, we perform a well-controlled investigation of the effect of postsynthetic water treatment of the as-prepared CsPbX3 NCs on the photoluminescence quantum yields (PLQYs) and stability, and one can find that the surface defective layer of CsPbX3 NCs can be dissolved into water and we can further separate the supernatant CsPbX3 NCs hexane solution from the water, which improves the PLQYs of CsPbCl3, CsPbBr3, CsPbI3 from 5%, 69.3%, 68.1% to 78.5%, 95.5%, 91%, respectively. As a synergetic effect, a trace amount of residual water facilitated the hydrolysis of tetramethyl orthosilicate, leading to the formation of SiO2-coated CsPbX3 NCs with high stability. The stable green-emitting CsPbBr3/SiO2 composite is used as an example to combine with red K2SiF6:Mn4+ to fabricate the light-emitting diodes device on the blue InGaN chip, which displays wide color gamut (128% of National Television Standard Committee standard), providing the possibility for liquid-crystal display backlight utilization.

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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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