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INORGANIC CHEMISTRY COMMUNICATIONS · 2026 · IF 5.9

Enhanced photocatalytic degradation of tetracycline hydrochloride by Zr-doped Bi₂₄O₃₁Cl₁₀: Synthesis, characterization, and reaction mechanism

Shuyan Qi,Yang Wang,Ling Guan,Xu Hu,Haiyang Li

This study addresses antibiotic water pollution by synthesizing Zr-doped Bi₂₄O₃₁Cl₁₀ (Bi₂₄(₁₋ₓ)Zr₁₈ₓO₃₁Cl₁₀) photocatalysts via hydrothermal method for tetracycline hydrochloride (TC-HCl) removal. Zr doping ratios (6–14%) were systematically investigated, with the optimal BZOC4 (12% Zr) degrading 91.24% of 20 mg/L TC-HCl within 120 min under 500 W xenon lamp irradiation (pH = 9). Its reaction rate constant (0.0239 min −1 ) is triple that of pristine Bi₂₄O₃₁Cl₁₀. Zr doping reduces the band gap from 3.12 eV to 2.8 eV, improves visible light utilization (absorption edge red-shifted to 525 nm), accelerates electron transfer, and reduces e − /h + recombination—supported by UV –Vis DRS, PL, and electrochemical tests. Superoxide radicals (O₂ − ·) and holes (h + ) are primary active species, confirmed by radical trapping and ESR. TOC analysis confirms 32.4% mineralization of TC-HCl to CO₂ and H₂O.This work offers new design strategies for bismuth halide-based photocatalysts in antibiotic remediation by integrating structural regulation and electronic modulation via Zr doping.

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ACS Omega · 2022 · IF 4.132

Tuning the Energetic Performance of CL-20 by Surface Modification Using Tannic Acid and Energetic Coordination Polymers

Bin Yuan,Yu Zhang,Ke-xin Wang,Tian-ping Wang,Yan Li,Shun-guan Zhu,Lin Zhang,Zhen-xin Yi,Hua Guan,Chen-guang Zhu

The energetic performance of hexanitrohexaazaisowurtzitane (CL-20) was modulated with two energetic coordination polymers (ECPs), [Cu(ANQ)2(NO3)2] and [Ni(CHZ)3](ClO4)2, in this study by a two-step method. First, tannic acid polymerized in situ on the surface of CL-20 crystals. Then, [Cu(ANQ)2(NO3)2] and [Ni(CHZ)3](ClO4)2 were hydrothermally formed on the surface of CL-20/TA, respectively. Explosion performance tests show that the impact sensitivity of the coated structure CL-20/TA/[Cu(ANQ)2(NO3)2] is 58% less than that of CL-20 with no energy decrease. On the other hand, CL-20/TA/[Ni(CHZ)3](ClO4)2 can be initiated by a low laser energy of 107.3 mJ (Nd:YAG, 1064 nm, 6.5 ns pulse width), whereas CL-20 cannot be initiated by even 4000 mJ laser energy. This study shows that it is feasible to modify the performance of CL-20 by introducing energetic CPs with certain properties, like high energy insensitive, laser-sensitive, etc., which could be a prospective method for designing high energy insensitive energetic materials in the future.

研究领域: 含能材料 · 材料化学 · 火炸药工程
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OPTICS EXPRESS · 2018 ·Vol. 26 ·期 16 ·20649-20660 · IF 3.356

High stability luminophores: fluorescent CsPbX3 (X = Cl, Br and I) nanofiber prepared by one-step electrospinning method

Maosen Yang,Jing Yu,Shouzhen Jiang,Chao Zhang,Qianqian Sun,Minghui Wang,Hang Zhou,Chonghui Li,Baoyuan Man,Fengcai Lei

The novel fluorescent nanofiber membranes of CsPbX3 (FNMs/CPX, X = Cl, Br, I) with a wide photoluminescence range from 405 nm to 675 nm are fabricated by a one-step electrospinning method in this paper. Owing to the polymer cladding, these FNMs/CPX show much better thermal and humid stability compared to the common CsPbX3 particles, and the corresponding white light-emitting diode prepared by them also exhibits excellent optical properties. Without adopting any complicated processes, this method opens up a brand new way for the perovskite materials using in lighting and display fields.

研究领域: 材料科学 · 光学工程
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Journal of Materials Chemistry A · 2019 ·Vol. 7 ·期 16 ·9761-9772 · IF 10.733

Dynamic Ag+-intercalation with AgSnSe2 nano-precipitates in Cl-doped polycrystalline SnSe2 toward ultra-high thermoelectric performance

Chengyan Liu,Zhiwei Huang,Dianhui Wang,Xiuxia Wang,Lei Miao,Xiaoyang Wang,Shaohai Wu,Nozomu Toyama,Toru Asaka,Junliang Chen,Eiji Nishibori,Li-Dong Zhao

Recently, thermoelectric lead-free selenides have attracted great attention due to their earth-abundant, low-cost and environment-friendly characteristics. Here we report a new strategy to simultaneously enhance the electronic transport properties and reduce the thermal conductivity of polycrystalline SnSe2. By combining weak van der Waals bonding with the mobile behavior of Ag+ ions, the carrier concentration is optimized over a wide temperature range, which can be attributed to the dynamic Ag+-intercalation into the van der Waals gap from the Ag+ ion reservoir AgSnSe2. On account of additional electrical bridges between interlayers contributed by the intercalated Ag+ ions and weak anisotropy, an exciting high power factor of up to ∼7.46 μW cm−1 K−2 at 789 K is achieved along the pressing direction. In addition, the thermal conductivity is simultaneously reduced to ∼0.57 W m−1 K−1 at 789 K, owing to numerous line defects, phase interfaces, twin boundaries, dislocations and intercalated atomic layers generated after Ag introduction, as well as the anharmonic vibration of Ag+ ions. As a result, a record peak ZT of ∼1.03 at 789 K is realized along the pressing direction, which is ∼1.6 times larger than the highest reported value (0.63) of polycrystalline SnSe2 and even comparable to that of p-type polycrystalline SnSe. This study opens a new way to achieve ultra-high thermoelectric performance, especially in layered materials.

研究领域: 材料科学 · 能源材料 · 凝聚态物理
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FUEL · 2023 · IF 7.4

Significantly different inhibition mechanisms of graphene oxide in laser-ignited combustion of micro and nano CL-20

Jiaxin Su,Yan Hu,Bin Zhou,Lizhi Wu,Yinghua Ye,Ruiqi Shen

Because of its high energy density, hexanitrohexaazaisowurtzitane(CL-20) has been widely used in propellants in place of conventional oxidizers. The adjustable burning rate of the CL-20 is a key factor in adapting the propellant to various environments. In this work, the effects of graphene oxide(GO) content on the thermal release, ignition and combustion characteristics of micro and nano CL-20 were thoroughly conducted based on the differential scanning calorimetry measurements (DSC), laser ignition, burning rate test and condensed combustion products collection. The results show GO has a positive effect on micro and nano CL-20 in ignition performance and a negative effect on combustion rate. Owing to the addition of GO, the original flameless combustion of CL-20 changes to flaming combustion. With increasing GO content, the burning rates of micro and nano CL-20 show completely different descending laws. Furthermore, the combustion mechanism of nano and micro CL-20/GO has been studied in detail. The burning rate of micro CL-20/GO is primarily determined by the condensed phase, and that of nano composite is controlled by both of the condensed and gas phases. This work provides a deeply insight into the influence mechanism of GO on the properties of nano and micro CL-20.

CAS / MDL: 110-54-3
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INORGANIC CHEMISTRY · 2023 · IF 4.6

Improvement on Magnetocaloric Effect through Structural Evolution in Gadolinium Borate Halides Ba2Gd(BO3)2X (X = F, Cl)

Yuwei Chen,Pifu Gong,Ruixin Guo,Feidi Fan,Jun Shen,Guochun Zhang,Heng Tu

A new Gd3+-containing borate Ba2Gd(BO3)2F has been successfully grown via the high-temperature solution method using BaF2-NaF-B2O3 flux. Ba2Gd(BO3)2F crystallizing in the orthorhombic space group Pnma is with lattice parameters a = 7.571(4) Å, b = 10.424(5) Å, c = 8.581(4) Å, α = β = γ = 90°, and Z = 2. Its three-dimensional framework was constructed from interesting pinwheel-like [Gd(BO3)F]∞ layers bridged by sharing [BO3]3–, which is different from the [Gd(BO3)]∞ layer in the model structure Ba2Gd(BO3)2Cl. The magnetic measurements indicated that Ba2Gd(BO3)2F has a larger magnetocaloric effect with −ΔSm,max = 27.82 J·kg–1·K–1at 2 K and 9 T than that of Ba2Gd(BO3)2Cl under the same conditions. Moreover, thermal stability, infrared spectrum (IR), and ultraviolet–visible-near-infrared diffuse reflectance spectrum were carried out to characterize the title compounds. The first-principles computations also looked into the electronic band structures, densities of states, and refractive indices.

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Energy Technology · 2016 ·Vol. 4 ·期 9 ·1112-1118 · IF 2.557

Aluminum-Ion Asymmetric Supercapacitor Incorporating Carbon Nanotubes and an Ionic Liquid Electrolyte: Al/AlCl3-[EMIm]Cl/CNTs

Handong Jiao,Junxiang Wang,Jiguo Tu,Haiping Lei,Shuqiang Jiao

An aluminum-ion asymmetric supercapacitor was assembled utilizing a cathode made of multi-walled carbon nanotubes (MWCNTs) in an ionic liquid 1-ethyl-3-methylimidazolium chloride ([EMIm]Cl)-based electrolyte. Two types of energy-storage mechanisms, that is, electrochemical double-layer capacitance (adsorption/desorption of AlCl 4 − on the surface) and limited intercalation pseudocapacitance (intercalation/deintercalation of AlCl 4 − in the graphite layer) at low current density, were observed and characterized. Meanwhile, the specific capacitance and cyclic stability of this supercapacitor were also evaluated by using galvanostatically charging–discharging. The result demonstrates that the specific capacitance decreases with increasing current density, which corresponds to the two types of energy-storage mechanisms of this device. The corresponding retention rate of this device after 3500 cycles at current density of 0.4 A g −1 was 82.4 %, which shows good cyclic stability.

CAS / MDL: 7446-70-0 308068-56-6
研究领域: 材料科学 · 电化学
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Journal of Environmental Sciences · 2018 · IF 3.12

Preparation of SGO-modified nanofiltration membrane and its application in SO42 − and Cl− separation in salt treatment

Yanjun Zhang,Changwei Zhao,Shaofeng Zhang,Ling Yu,Jiding Li,Li-an Hou

The lack of fresh water in the world makes the search for an effective method to decontaminate water an urgent priority. An important step is to remove different multivalent ions in salt treatment. Nanofiltration (NF) has been used for treating water containing different kinds of salts. In this work, sulfonate group-modified graphene oxide (SGO) was prepared, and added during the interfacial polymerization (IP) reaction to prepare SGO-modifiedNF membranes (PA-SGO). The chemical composition, structure and surface properties of PA and PA-SGO membranes were characterized by FT-IR, XPS, SEM, AFM, contact angle and zeta potential measurements. Their water flux , salt rejection and anti-fouling abilities were investigated systematically. The testing results showed that the water flux of PA-SGO (0.03% SGO) was 45.85 LMH under a pressure of 0.2 MPa, and the salt rejection varied in the order of Na 2 SO 4 (98.99%) > MgSO 4 (91.25%) > MgCl 2 (42.27%) > NaCl (21.96%). An anti-fouling experiment indicated that the PA-SGO membrane had good anti-fouling properties because of its decreased roughness and increased hydrophilicity and electronegativity. The PA-SGO membrane has good potential for use in removing salt ions from water.

CAS / MDL: 112726-66-6 2370-88-9
研究领域: 环境科学 · 材料科学 · 水处理
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CHEMISTRY-A EUROPEAN JOURNAL · 2017 ·Vol. 24 ·期 8 ·1898-1904 · IF 5.317

Highly Luminescent CsPbX3 (X=Cl, Br, I) Nanocrystals Achieved by a Rapid Anion Exchange at Room Temperature

Shaofan Fang,Guangshe Li,Yantong Lu,Liping Li

Graphical Lifting the curse : We reported on a novel route by using solid metal halides as halide sources that achieve an anion exchange with CsPbX 3 without any pretreatment. Introducing small amounts of oleic acid or oleylamine speed up the exchange reaction rate, although showing different promotion mechanisms (see figure). Cesium lead halide perovskite (CsPbX 3 ) nanocrystals (NCs) exhibit an excellent photoelectric performance, which is directly governed by fine-tuning of the composition and preparation of materials with a special phase structure and morphology. However, it is still facing challenges to achieve highly stable and luminescent CsPbX 3 NCs at room temperature. Herein, we report on a novel exchange reaction, in which metal halides MX 2 (M=Zn, Mg, Cu, or Ca; X=Cl, Br, or I) solids act as anion source to directly prepare CsPbX 3 NCs at room temperature without any pretreatment. Introducing small amount of oleic acid or oleylamine speed up the exchange reaction through different promotion mechanisms. Oleic acid coordinates to the surface of the NCs, which increases the reaction activity, and oleylamine greatly enhances the dissolution of ZnCl 2 . XRD and TEM tests demonstrate that the cubic phase structure and the morphology of the parent CsPbX 3 were well preserved. Moreover, the band-gap energies and photoluminescence (PL) spectra were readily tunable over the entire visible spectral region of λ =406–685 nm. Our findings could open up the possibilities of using metal halide solids as new anion sources to prepare high-quality CsPbX 3 NCs at room temperature.

研究领域: 材料科学 · 化学
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Journal of Water Process Engineering · 2023 · IF 7

Enhanced selective nitrate-to-nitrogen electrocatalytic reduction by CNTs doped Ni foam/Cu electrode coupled with Cl−

Xinrui Liu,Rui Guo,Xia Qin,Cuicui Xu

In this work, a Ni foam/CNTs/Cu composite electrode was prepared via the impregnation and electrodeposition methods. The electrode enhanced the total nitrogen removal and N 2 selectivity , when served as a cathode for NO 3 − -N reduction. SEM, EDS, XRD, and XPS characterization revealed that both CNTs and metallic copper were introduced onto the surface of the Ni foam substrate successfully. Besides, the LSV, CV, EIS and C dl results indicated more electrochemical active sites were in the Ni foam/CNTs/Cu electrodes than in Ni foam/Cu electrodes. Under optimal preparation conditions, the Ni foam/CNTs/Cu electrode showed N 2 selectivity of 68.89 % and nitrate removal rate of 96.75 % in 100 mg/L nitrate solution with Na 2 SO 4 as electrolyte. The selectivity of N 2 could be significantly enhanced by adding Cl − as electrolyte, and the nitrogen selectivity increased with the increase of Cl − concentration. At 1.25 g/L NaCl, the Ni foam/CNTs/Cu electrode could achieve >95 % nitrate and total nitrogen removal and close to 100 % N 2 selectivity. The N 2 selectivity of the Ni foam/CNTs/Cu electrode was 2.534 and 1.8 times of the Ni foam/Cu electrode when 0.5 g/L Na 2 SO 4 and 0.5 g/L NaCl were used as electrolytes, respectively. Consequently, to achieve the same nitrate reduction effect, the Ni foam/CNTs/Cu electrode could reduce the amount of NaCl compared with Ni foam/Cu electrode. The electrodes were tested in 6 cycles and proved to be stable. At last, a potential mechanism of nitrate‑nitrogen removal by the electrocatalytic process was suggested.

CAS / MDL: 7697-37-2 7664-93-9
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Journal of Materials Chemistry C · 2023 ·Vol. 12 ·期 3 ·922-929 · IF 6.4

Fast solution-phase growth of centimeter-sized Cs3Cu2X5 (X = Cl, I) single crystals for high-performance scintillators

Xiangshi Bin,Jiaxing Liu,Ruosheng Zeng,Hongbang Liu,Jialong Zhao,Tao Lin

Fast and convenient synthesis of zero-dimensional (0D) cesium-copper(I) halide (Cs3Cu2X5 (X = Cl, I)) single crystals (SCs) is critical to achieve practical radiography. In this study, rapid growth of high-quality Cs3Cu2X5 (X = Cl, I) SCs with sizes reaching centimeter scale were achieved within 24 hours using scalable solution-phased methods. These crystals exhibited highly effective emission with large Stokes shifts, excellent PL linearity, and PLQYs exceeding 86%. Additionally, post-treated Cs3Cu2X5–PMMA films demonstrated outstanding scintillation performance, including excellent stabilities, light yield surpassing 36 000 photons per MeV, and spatial resolution up to 6.5 lp per mm in X-ray imaging tests. The high scintillation efficiency can be attributed to their compact 0D crystalline structure, resulting in a small defect density and strong exciton localization.

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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Facilitating the Carrier Transport Kinetics at the CsPbBr3/Carbon Interface through SbX3 (X = Cl, Br, I) Passivation

Wenwen Liu,Teng Zhang,Baohua Zhao,Chengben Liu,Youru Bai,Zhi Li,Shihui Zhu,Tailin Wang,Xinyu Sun,Heyuan Liu,Zhaobin Liu,Yanli Chen,Xiyou Li

The nonradiative carrier recombination at the perovskite/carrier selective layer (CSL) interface was accounted for the inferior power conversion efficiency (PCE) of perovskite solar cells (PSCs), especially rigid all-inorganic perovskite (CsPbI3 and CsPbBr3). In this study, targeting the poor interface, we introduce SbX3 (X = Cl, Br, I) surface passivation at the CsPbBr3/carbon interface. Smoothed compressive strain, reduced defect density, and enhanced energy-level alignment were achieved simultaneously, facilitating carrier extraction at the selective interface. With the simple aqueous solution-based two-step process, the PCE of our SbI3 passivated carbon-based CsPbBr3 PSCs has increased from 7.81% (without passivation) to 9.69%, a ∼25% enhancement. Specifically, Voc (1.657 V) of the SbI3-passivated cells was much higher than that of the control ones (1.488 V), confirming the ameliorated interface. Finally, our unencapsulated SbI3 passivated devices maintain 90% of their initial PCEs while left in the air for 30 days with a relative humidity of 60%. To conclude, we present an interfacial carrier extraction-enhanced strategy for preparing high-performance and stable CsPbBr3-based PSCs.

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