Advanced Science
·
2022
·Vol. 10
·期 4
·2204755
·
IF 17.521
Shaoxin Cui,Hongping Wu,Zhanggui Hu,Jiyang Wang,Yicheng Wu,Hongwei Yu
Oxychalcogenides capable of exhibiting excellent balance among large second-harmonic generation (SHG) response, wide band gap ( E g ), and suitable birefringence (Δ n ) are ideal materials class for infrared nonlinear optical (IR NLO) crystals. However, rationally designing a new high-performance oxychalcogenide IR NLO crystal still faces a huge challenge because it requires the optimal orientations of the heteroanionic groups in oxychalcogenide. Herein, a series of antiperovskite-type oxychalcogenides, Ae 3 Q[GeOQ 3 ] (Ae = Ba, Sr; Q = S, Se), which were synthesized by employing the antiperovskite-type Ba 3 S[GeS 4 ] as the structure template. Their structures feature novel three-dimensinoal frameworks constructed by distorted [QAe 6 ] octahedra, which are further filled by [GeOQ 3 ] tetrahedra to form antiperovskite-type structures. Based on the unique antiperovskite-type structures, the favorable alignment of the polarizable [GeOQ 3 ] tetrahedra and distorted [QAe 6 ] octahedra have been achieved. These contribute the ideal combination of large SHG response (0.7–1.5 times that of AgGaS 2 ), wide E g (3.52–4.10 eV), and appropriate Δ n (0.017–0.035) in Ae 3 Q[GeOQ 3 ]. Theoretical calculations and crystal structure analyses revealed that the strong SHG and wide E g could be attributed to the polarizable [GeOQ 3 ] tetrahedra and distorted [QAe 6 ] octahedra. This research provides a new exemplification for the design of high-performance IR NLO materials.
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JOURNAL OF LUMINESCENCE
·
2022
·
IF 4.171
Kaiming Zhu,Zhanglin Chen,Yuzhen Wang,Hui Liu,Yude Niu,Xin Yi,Yihuan Wang,Xuanyi Yuan,Guanghua Liu
Eu 2+ -doped CaAlSiN 3 ‐type structure nitrides have been extensively studied as a red-emitting phosphors in white light emitting diodes (w-LEDs), but there are few reports of systematic research on the effect of solid solution substitution on their long persistent luminescent properties. In this work, a series of (M,Ca)AlSiN 3 :Eu 2+ (M = Sr, Mg) phosphors have been successfully synthesized by efficient combustion synthesis . We investigated the effect of Sr and Mg solid solution on long persistent luminescent properties. Thermoluminescence (TL) measurements were performed in those persistent phosphors to obtain direct experimental results on the trap depth. The results show that the SrAlSiN 3 :0.2 at% Eu 2+ phosphor exhibits the most intense red persistent luminescence with the persistent time of as long as 200 min at the threshold value of 0.32 mcd/m 2 due to the presence of more trap levels with suitable depths of 0.71 eV. Compared with the solid solution of Sr, the solid solution of Mg ions can increase the depth of trap levels in CaAlSiN 3 . Among them, Mg 0.2 Ca 0.8 AlSiN 3 :0.2 at% Eu 2+ phosphor achieved a maximum trap depth of 0.98 eV, making it a promising candidate for optical information storage applications.
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JOURNAL OF HAZARDOUS MATERIALS
·
2021
·
IF 10.588
Jiangbo Huo,Guoce Yu,Jianlong Wang
In this study, a novel adsorbent, polyvinyl alcohol/graphene oxide/MnO 2 composite was prepared, characterized and used for efficient removal of Co 2+ and Sr 2+ from aqueous solution. Polyvinyl alcohol (PVA) and Mn 2+ played a synergistic role in the gelation of PVA/GO/Mn 2+ , while Mn 2+ can be further converted into oxide to achieve functionalized aerogel (PVA/GO/MnO 2 ). The spectroscopy analysis manifested that hydrogen bonds and electrostatic attraction were responsible for the formation of PVA/GO/MnO 2 . The functionalization of MnO 2 enhanced the adsorption capacity for Co 2+ (2.1 folds) and Sr 2+ (1.3 folds) by PVA/GO/MnO 2 . The composite showed high adsorption capacity at broad pH range of 4.0–9.0. For competitive adsorption test, Ni 2+ /Zn 2+ exerted the most interfering effect on Co 2+ adsorption, while Mg 2+ /Ca 2+ showed severe interfering effect on Sr 2+ adsorption. Both electrostatic attraction and oxygen-containing groups contributed to the adsorption mechanism. This study may provide a new adsorbent for separation of Co 2+ and Sr 2+ from aqueous solution.
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RSC Advances
·
2016
·Vol. 6
·期 60
·54679-54692
·
IF 3.289
Yan Liu,Fangfang Liu,Liang Ni,Minjia Meng,Xiangguo Meng,Guoxing Zhong,Jian Qiu
In this paper, response surface methodology (RSM) was successfully applied for the first time to optimize the dynamic adsorption conditions for the maximum removal of Sr(II) ion from aqueous solutions using Sr(II) ion imprinted polymers (Sr(II)-IIPs) as adsorbents. Sr(II)-IIPs based on the support matrix of magnetic SBA-15 (Fe3O4@SBA-15) were prepared by a surface imprinted technique and RAFT polymerization. The adsorbents can be separated from the fixed-bed column after adsorption by an external magnetic field. The effects of the operational parameters for maximizing Sr(II) removal were studied using Box–Behnken design (BBD) combined with RSM. A second-order quadratic model was built to predict the responses. The significance of the independent variables and their interactions was studied and tested by analysis of variance (ANOVA). The adequacy of the model was tested by the correlation between the experimental and predicted values of the responses. At optimum adsorption conditions, the Sr(II) adsorption capacity of Sr(II)-IIPs was found to be 22.12 mg g−1. Moreover, Sr(II)-IIPs exhibited an excellent dynamic selectivity of Sr(II) and could be easily regenerated by a dynamic desorption process with a desorption ratio of 99.2%.
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ACS Sustainable Chemistry & Engineering
·
2024
·
IF 7.1
Jitong Deng,Yanan Zhang,Hongjing Han,Yongjun Zhang,Haiying Wang,Xuzhong Gong,Yanguang Chen
The chemical looping conversion of CH4 has been one of the most promising technologies for achieving the “two-carbon” strategy. Fe2O3 oxygen carrier cannot maintain the excellent release performance of lattice oxygen at high temperature due to the sintering and carbon deposition. Therefore, quaternary La1–xSrxFe1–y CoyO3 perovskite was selected as the transfer support of oxygen ions. By using the MOF precursor method, ternary La0.8Sr0.2FeO3 was prepared via the introduction of metal Sr into the binary LaFeO3. The adsorption energy of CH4 on the La0.8Sr0.2FeO3 was the lowest (−0.054 eV), compared with separate Fe2O3 and LaFeO3, and the adsorption energy of free H at the adjacent Fe site was the lowest (1.650 eV). Furthermore, the La1–xSrxFe1–yCoyO3 perovskite was successfully synthesized by the doping of Co into the ternary La0.8Sr0.2FeO3. La0.8Sr0.2Fe0.8Co0.2O3 was chosen to composite Fe2O3 oxygen carrier. As m(Fe2O3):m(La0.8Sr0.2Fe0.8Co0.2O3) = 1:1, the lattice oxygen conversion rate was less than 47% and the selectivity of CO2 reached 99.5% through the synergistic effect of lattice oxygen and oxygen vacancies. Fe2O3–La0.8Sr0.2Fe0.8Co0.2O3 increased the lattice oxygen conversion by 17.6%, compared with Fe2O3–La0.8Sr0.2FeO3. After the CH4 chemical looping conversion cycles five times, Fe2O3–La0.8Sr0.2Fe0.8Co0.2O3 still had favorable structural stability and oxidation performance, and the lattice oxygen conversion rate still reached >95%.
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JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS
·
2024
·
IF 5.8
Shuna Zhao,Hao Liu,Mi Li,Lin Jiang
5-Aminotetrazole/strontium nitrate (5AT/Sr(NO 3 ) 2 ) propellant is widely utilized as green gas generating agent in fire extinguishers. To enhance the combustion rate and modify the gas production performance of 5AT/Sr(NO 3 ) 2 propellant, this study investigated the catalytic effects of adding different metal oxides (Bi 2 O 3 , PbO, TiO 2 , and CoO) on its pyrolysis and combustion process. The pyrolysis behavior, pyrolysis mechanism and combustion performance of 5AT/Sr(NO 3 ) 2 propellants were studied by using thermogravimetry (TG), derivative thermogravimetry (DTG), differential scanning caborimetry (DSC), mass spectrometry (MS), fourier transform infrared spectroscopy (FTIR) analysis and closed bomb vessel tests. Experimental results indicated that Bi 2 O 3 and PbO predominantly facilitated the thermal decomposition process of 5AT, while TiO 2 and CoO primarily catalyzed the thermal decomposition of Sr(NO 3 ) 2 . Certainly, the addition of metal oxides as catalysts to 5AT/Sr(NO 3 ) 2 propellant holds significant potential for improving the application as a gas generating agents in fire extinguishers.
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JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS
·
2022
·Vol. 39
·期 10
·2625-2636
·
IF 2.058
Hang Liu,Xingke Zheng,Pengcheng Wang,Haiyan Wang,Yuhong Zhang
In this work, a comparative study of the upconversion (UC) luminescence properties of ${{\rm Er}^{3 +}} {-} {{\rm Yb}^{3 +}}$-co-doped ${{\rm AWO}_4}$ (${\rm A} = {\rm Ba}$, Sr, and Ca) scheelite phosphors and ${{\rm Er}^{3 +}} {-} {{\rm Yb}^{3 +}} $-co-doped ${{\rm MgWO}_4}$ wolframite phosphors is reported. Under 980 nm excitation, all the samples emit green and red emissions. The ${{\rm Er}^{3 +}} {-} {{\rm Yb}^{3 +}}$-doped ${{\rm MgWO}_4}$ phosphor has a higher UC emission intensity. Furthermore, the optical temperature sensing properties in ${{\rm Er}^{3 +}} {-} {{\rm Yb}^{3 +}}$-co-doped ${{\rm AWO}_4}$ (${\rm A} = {\rm Ba}$, Sr, Ca, and Mg) phosphor samples are investigated. The relative sensitivity (${{\rm S}_r}$) based on thermally coupled levels (TCLs) increases gradually with an increase in matrix phonon energy. The absolute sensitivity (${{\rm S}_a}$) values of the samples are accurately predicted by the chemical bonding parameter (${{\rm f}_c}$). The results of the correlation between the UC luminescence properties and the microscopic crystal structure, and the relationship of the temperature sensitivity and the host parameters, provide us with a guiding insight for the selection of a host material with ideal temperature measurement capability.
研究领域:
材料科学
·
光学
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ChemCatChem
·
2026
·Vol. 18
·期 13
·e70894
·
IF 4.1
Siqi Tan,Jie Gu,Kexin Sha,Yihan Jiao,Yanxi Wu,Yiru Wang,Hongjian Yu,Jie Han
Niobates have emerged as promising candidates for environmental catalysis, particularly in the realm of piezocatalysis, owing to their distinctive layered architectures and robust physicochemical performance. In this study, we report the successful fabrication of A-site cation-tailored ABi 2 Nb 2 O 9 (A = Sr, Ca, and Ba) layered oxides via a molten salt strategy. Notably, the molten salt-synthesized SrBi 2 Nb 2 O 9 exhibits superior piezocatalytic performance in H 2 O 2 evolution with a yield reaching 1836.1 µmol g −1 h −1 , approximately 2.1 times higher than that of SrBi 2 Nb 2 O 9 prepared by the solid-state method. Furthermore, this material demonstrates exceptional piezocatalytic activity, degrading 98.0% of Rhodamine B within 75 min, with a reaction rate constant of 0.04966 min −1 . In addition, the catalyst shows durable stability, maintaining 97% of its original activity after four cycles. The influence of environmental factors, including solution pH and inorganic anions (Cl − and CO 3 2− ), was also systematically evaluated. This work elucidates that the synergistic integration of A-site cation engineering and molten salt synthesis effectively modulates the piezoelectric response of ABi 2 Nb 2 O 9 (A = Sr, Ca, and Ba), offering new insights and a viable pathway for the design of novel, high-performance piezocatalysts for environmental remediation. Graphical Molten salt-mediated A-site cation engineering of ABi 2 Nb 2 O 9 effectively modulates piezoelectric response, achieving superior piezocatalytic H 2 O 2 production and pollutant degradation. This work provides a viable pathway for designing high-performance piezocatalysts for environmental remediation.
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CERAMICS INTERNATIONAL
·
2025
·
IF 5.6
Jie Li,Ziyi Zhang,Hongji Zou,Ying Tang,Weiping Gong,Liang Fang
Dense ALaGa 3 O 7 (A = Ba, Sr, Ca) ceramics with tetragonal melilite structure were prepared by the solid-phase method. The optimal microwave dielectric properties were obtained with ε r = 11.1 ± 0.1, 11.3 ± 0.1, 13.3 ± 0.1; Q × f = 49,400 ± 300, 31,100 ± 300, 17,100 ± 300 GHz; and τ f = −41.5 ± 1.0, −36.6 ± 1.0, −28.8 ± 1.0 ppm/°C for BaLaGa 3 O 7 , SrLaGa 3 O 7 , and CaLaGa 3 O 7 , respectively. The increased ε r and τ f while reduced Q × f in the order of BaLaGa 3 O 7 , SrLaGa 3 O 7 , and CaLaGa 3 O 7 were mainly due to the enhanced rattling effect of A-site, which resulted in large positive discrepancy Δ ε r between ε r ( Corr ) and ε r (C-M) increasing from +31.8 % to +74.7 %. The vibration modes, chemical bond characteristic and intrinsic dielectric properties were analysed by Raman, P-V-L theory, and far-infrared reflectance spectroscopy. Additionally, a dielectric resonator antenna based on BaLaGa 3 O 7 ceramic was designed with a bandwidth of 270 MHz at 6.8–7.1 GHz and a gain of 5.6 dBi at 6.9 GHz, indicating the potential candidate for dielectric resonator antennas.
研究领域:
材料科学
·
电子功能材料
·
微波技术
·
无机非金属材料
·
介电材料
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Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 2
·121155
·
IF 7.2
Yaqi Liu,Hui Lu,Changfei Gao,Yameng Wang,Haoran Liu,Huiqiang Ma,Bo Wang,Lifen Liu,Yihua Li,Xianbo Chang
The persistent threat posed by radioactive metal contamination necessitates the development of innovative and sustainable remediation strategies. In this study, we proposed a self-sustaining bioelectrocatalytic reduction system (BECRs) incorporating an in situ co-synthesized ternary Fe/Cu/Co@Z-CF cathode derived from zeolite imidazole salt skeleton (ZIF) -functionalized carbon felt. The engineered electrode demonstrated outstanding electrocatalytic performance, characterized by an ultrahigh exchange current density of 7.68 × 10 −3 A cm −2 and minimal charge transfer resistance of 0.11 Ω. These properties were attributed to the synergistic redox cycling of Fe-Cu-Co species and the enhanced exposure of active sites facilitated by the ZIF structure. Under optimized conditions at pH 11, the BECRs achieved removal efficiencies exceeding 98.28 % for targeted radionuclides (Cs + : 99.00 %, Sr 2+ : 98.28 %, Tb 3+ : 99.95 %, Eu 3+ : 99.97 %) while generating a stable bio-voltage of 730 mV. The removal mechanisms operated synergistically through three primary pathways: direct electroreduction of metals to elemental or metallic oxide forms at the catalytic cathode; electroflocculation mediated by in situ formation of Fe(OH) x species and microbial adsorption by enriched pollutant-resistant microbial consortia, notably with a 16.3 % increase in Bacteroidota abundance. Density Functional Theory (DFT) calculations revealed charge complementarity among Fe/Cu/Co sites, accelerating oxygen reduction kinetics. Crucially, the electrode demonstrated negligible metal leaching across pH 3–11, confirming ecological safety. Kinetic analysed distinguish radionuclide-specific pathways: pseudo-first-order for Cs⁺/Sr²⁺ versus pseudo-second-order for Tb 3+ /Eu 3+ , informing selective recovery strategies. This work established a green, energy-positive paradigm for radioactive wastewater treatment, achieving simultaneous decontamination, resource recovery (metallic Cs/Sr/Tb/Eu) with significant potential for closed-loop nuclear effluent management.
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CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Pengfei Gao,Yangpeng Zuo,Yulu Yang,Jinxiu Yu,Wuzhe Fan,Ruqing Bai,Weihu Yang,Kaiyong Cai
To resolve the short-term inflammatory storm after the operation and the long-term osteointegration deficiency of titanium (Ti) implant as an artificial hip joint, in this work, a novel functionalized Ti implant with an “on-demand” treatment strategy was explored. The metallopolyphenol network (Epigallocatechin gallate (EGCG) and Strontium) wrapped Prussian blue nanoparticles were prepared and anchored on the Ti surface. During the acute inflammatory phase, the inflammatory acidic microenvironment will result in the degradation of the metallopolyphenol network and the responsive release of EGCG and strontium (Sr) ions. The released EGCG could reduce oxidative stress damage and promote the transition of macrophages from M1 to M2. In comparison, Sr ions could stimulate osteoblast differentiation and achieve the rapid osteogenesis and fixation of implants. To achieve long-term osteointegration efficacy, “on-demand” near-infrared light irradiation for the remained PB particles could be adopted if necessary. The mild photothermal conversion temperature could upregulate the expressions of heat shock proteins around the implant and promote the biosynthesis of type I collagen, as well as the formation of bone matrix. In vitro and in vivo results proved the feasibility of our strategy. It is a prospective method for the modification of Ti implants.
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY
·
2022
·Vol. 103
·期 3
·865-875
·
IF 2.606
Jia Jiannan,He Mengting,Wang Yunpeng,Zhang Wei,Wan Jun,Zhang Yuting,Xu Qiang,Chen Shiguo,Qiao Xvsheng,Fan Xianping
A propylene oxide (PO)-driven fast sol-gel route followed with a post high temperature calcination were utilized to synthesize Ca x Sr 1- x Al 2 O 4 : Eu 2+ cationic solid solution phosphors with micro-spherical morphologies and improved internal quantum efficiencies. The polyethylene oxide (PEO) was also employed to induce the phase separation of Ca x Sr 1- x Al 2 O 4 : Eu 2+ precursors to get monodispersed spherical morphologies in the sol-gel system. Benefit from uniform copolymerization of each chemical components and pyrolysis of organic matter, Ca, Sr, Al and O were homogenously distributed in the produced Ca x Sr 1- x Al 2 O 4 : Eu 2+ cage like microspheres. It helps to efficiently trap incident light and to improve the PL efficiencies. By changing the ratio of Ca/Sr, infinite solid solution polycrystalline phosphors, Ca x Sr 1- x Al 2 O 4 : Eu 2+ microspheres with x = 0~1, can be obtained and their PL emission can be gradually tuned from green to white to blue. Micro-spherical SrAl 2 O 4 : Eu 2+ , Ca x Sr 1- x Al 2 O 4 : Eu 2+ and CaAl 2 O 4 : Eu 2+ phosphors exhibited internal quantum efficiencies as high as 71.1, 35.3~45.9 and 75.3%, respectively.
Graphical abstract
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危险品化学品经营许可证（带存储）