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Z-scheme Bi4O5Br2/NH2-MIL-125（Ti） heterojunctions enable exceptional visible photocatalytic degradation of organic pollutant

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Rare Metals 2024年第7期43卷 3161-3172页

作者： Feng Huang Muhammad Humayun Gang Li Ting-Ting Fan Wen-Lin Wang Yu-Lin Cao Anton Nikiforov Chun-Dong Wang Jing Wang Key Laboratory of Analytical Science and Technology of Hebei Province Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of the Ministry of EducationState Key Laboratory of New Pharmaceutical Preparations and ExcipientsCollege of Chemistry and Materials ScienceHebei University Energy Water and Environment LabCollege of Humanities and SciencesPrince Sultan University Baoding Green Yijia Environmental Protection Technology Ltd Physics Laboratory Industrial Training CenterShenzhen Polytechnic University Department of Applied Physics Ghent University School of Integrated Circuits Wuhan National Laboratory for OptoelectronicsHuazhong University of Science and Technology

One key strategy to enhance photocatalytic performance is to improve the transfer and separation efficiency of photogenerated carriers by building optimized ***,novel Bi4O5Br2/NH2-MIL-125（Ti）Z-scheme heterojunctions are fabricated and used as photocatalysts for organic pollutant *** NH2-MIL-125（Ti） nanosheets are exfoliated via a self-developed alkali solution stripping approach and then uniformly decorated on *** as-prepared Bi4O5Br2/NH2-MIL-125（Ti） presents more than 90% degradation of various pollutants,outperforming the counterpart individual *** various characterization results suggest that the enhanced degradation rate is due to the more intimate face-to-face interfacial contact of the lamellar Z-scheme heterojunction materials,in which the migration path of carriers from the material's interior to the surface can be reduced,in turn enhancing migration efficiency and separation capability significantly.A possible photocatalytic reaction mechanism is proposed based on the photoelectric behaviors,radical trapping experiments and liquid chromatography mass spectrometry *** work promotes the development of new photocatalytic materials for heterojunctions with face-to-face interfacial contacts,as well as the effective purification of wastewater in environmental remediation.

关键词： Z-scheme heterojunctions Photocatalysis Alkaline solution stripping Bi 4 O 5 Br 2 NH 2 -MIL-125(Ti)

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Dual modification of LiNi0.83Co0.11Mn0.06O2 cathode materials by K+ doping and Li3PO4 coating for lithium ions batteries

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Rare Metals 2024年第7期43卷 3007-3018页

作者： Wei Xiao Jia-Le Wang Zhi-Cheng Yi Cheng-Jin Liu Chang Miao Yu Xin Shu-Qing Nie College of Chemistry and Environmental Engineering Yangtze University

Li3PO4@Li0.99K0.01Ni0.83Co0.11MnO.06O2（NCM-KP） cathode powders are synthesized via K+doping in calcination processes and H3PO4coating in sol-gel processes.K+precisely enters into the lattice to widen the（003） plane to 0.4746 nm with a lower cationic disordered degree of 1.87%.Moreover,the surface residual lithium salts are treated by H3PO4to generate a uniform Li3PO4coating layer of approximately 11.41 nm,which completely covers on the surface of secondary spherical particles to improve the interfacial *** 25℃,the NCM-KP electrode delivers a discharge specific capacity of 148.9 mAh·g-1with a remarkable capacity retention ratio of 84.1% after 200 cycles at 1.0C and retains a high reversible specific capacity of 154.4 mAh·g-1at *** at 1.0C and 60℃,it can maintain a reversible discharge specific capacity of 114.6 mAh·g-1with 0.21% of capacity decay per cycle after 200 cycles,which is significantly lower than 0.40% for the pristine NCM ***,the charge transfer resistance of 238.89 Ω for the NCM-KP electrode is significantly lower than 947.41 Ω for the pristine NCM one by restricting the interfacial side ***,combining K+doping and Li3PO4coating is an effective strategy to enable the significant improvement of the electrochemical property of high-nickel cathode materials,which may be mainly attributed to the widened diffusion pathway and the formed Li3PO4protective layer,thus promoting Li+diffusion rate and preventing the erosion of HF.

关键词： High-nickel cathode material Residual lithium K + doping Li 3 PO 4 coating Lithium ions battery

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Coupling N-doping and confined Co3O4 on carbon nanotubes by polydopamine coating strategy for pleiotropic water purification

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Rare Metals 2024年第7期43卷 3146-3160页

作者： Wen-Long Tu Gang Wang Yue Zhang Hong-Yang Zhu Rong-Rong Du Hong-Yao Zhao Sheng Tang Zeng-Jing Guo Jun Yang Fu Yang Cheng-Zhang Zhu School of Environmental and Chemical Engineering Jiangsu University of Science and Technology School of Chemistry and Chemical Engineering Liaocheng University School of Material Science and Engineering Jiangsu University of Science and Technology School of Environmental Science and Engineering Nanjing Tech University

The development of effective and sustainable solutions for pleiotropic water purification becomes urgent and *** Fenton-like catalysts for activation of peroxymonosulfate（PMS） to purify organic wastewater show great *** this work,by tuning metal loading with an in-situ polydopamine coating strategy,oxygen vacancy-enriched Co3O4loading on N-doped carbon nanotubes（CNTs） were constructed to enhance PMS activation efficiency for pollutants ***,the obtained modified CNTs afford a well-developed N-containing network structure,which is further endowed with abundant Co（Ⅱ）/Co（Ⅲ） redox cycles and significant metal-carbon *** particular,the surface N doping in CNTs might induce the oriented enrichment of pollutants around the catalyst,which reduces the migration distance and correspondingly improves the utilization of reactive oxidative *** electron transfer efficiency of the catalyst can be further improved by incorporating oxygen vacancy-enriched *** performance results show that the optimal NC/Co-1 could mineralize 20 × 10-6of bisphenol A（BPA） by almost 98% in 8 min.A low reaction activation energy(26.05 kJ·mol-1) in BPA degradation was demonstrated by the NC/*** importantly,NC/Co-1 can inherit excellent degradation performance towards oxytetracycline,2,4-dichlorophenol,and tetracycline,showing wide practical *** addition,by virtue of the photothermal conversion property,NC/Co-1 achieves an additive function for interfacial solar water evaporation(1.84 kg·m-2·h-1,112.51%),showing impressive potential for clean water recovery under complicated environmental pollution conditions.

关键词： Carbon nanotube Advanced oxidation process Co 3 O 4 Photothermal conversion Solar water evaporation

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Effect of Eu3+,Bi3+,and Li+ doping on luminescent property of GdNbO4

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Journal of Rare Earths 2024年第1期42卷 66-75页

作者： S.W.Wi Y.S.Lee Department of Physics and Integrative Institute of Basic Sciences Soongsil University

We investigated the emission properties of Eu3+-doped GdNbO4-based oxide phosphors,aiming at improving the Eu3+emission by codoping of Bi3+and Li+.Eu3+singly doped,Eu3+and Bi3+doubly doped,and Eu3+,Bi3+,and Li+triply doped GdNbO4were prepared using a high-temperature solid-state reaction *** red-orange emissions from Eu3+in the singly doped samples are significantly improved by the codoping of Bi3+,mainly due to the energy transfer from Bi3+to Eu3+.The additional codoping of Li+is found to increase the Eu3+emission *** improvement might be attributed to the increase in the photoluminescent quantum yield originating from larger grain sizes and better crystallinity.A detailed analysis of the X-ray diffraction pattern and the asymmetric ratio estimated from the photoluminescence spectra show that the local lattice environment around Eu3+in GdNbO4does not change significantly with the codoping of Bi3+and Li+.Our results indicate that Li+doping is a promising way to improve the emission properties of rare-earth ion-doped GdNbO4phosphors.

关键词： Eu 3+ GdNbO 4 Codoping of Li + Photoluminescence Sensitizer Rare earths

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Insights into photocatalytic mechanism over a novel Cu2WS4/MoS2 S-scheme heterojunction

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Rare Metals 2024年第7期43卷 3118-3133页

作者： Wei Zhao Ji-Hui Cao Jun-Jie Liao Yun Liu Xiao-Jun Zeng Jun-Yu Shen Xue-Kun Hong Yang Guo He-Hua Zeng Ya-Zi Liu School of Materials Engineering Jiangsu Key Laboratory of Advanced Functional MaterialsSchool of Electronic and Information EngineeringChangshu Institute of Technology School of Chemistry and Chemical Engineering Changji University State Environmental Protection Key Laboratory of Soil Environmental Management and Pollution Control Ministry of Ecology and EnvironmentNanjing Institute of Environmental Sciences School of Environment Jiangsu Engineering Lab of Water and Soil Eco-RemediationNanjing Normal University Department of Chemical Engineering Curtin University

A novel efficient Cu2WS4/MoS2step-scheme（S-scheme） heterojunction photocatalyst was constructed for the first time and applied in the removal of environmental *** the as-prepared photocatalysts,the Cu2WS4/MoS2-8 % heterojunc tion photoc atalyst demonstrates the optimal photocatalytic performance,with the catalytic oxidation efficiency of tetracycline（TC） and the catalytic reduction efficiency of Cr6+reaching 93.3%and 82.1 %,*** excellent catalytic properties of Cu2WS4/MoS2heterojunction photocatalysts are attributed to the effective separation pathways of charges and the presence of S-scheme heterojunctions,together with stronger redox *** is speculated that the photogenerated carrier migration path of the Cu2WS4/MoS2catalyst follows the typical S-scheme photocatalytic mechanism,which is verified by the in-depth experimental study and simulated calculations including the electron paramagnetic resonance（EPR） analysis,free radical quenching experiments,charge density distribution,and simulated built-in electric field formation at the interface,which acts as driving force to promote the separation of photoinduced electrons and ***,the photocatalytic mechanism of S-scheme photogenerated carrier migration for the Cu2WS4/MoS2catalyst is revealed based on the systematic experimental techniques and simulated calculations,accounting for its superior photocatalytic oxidation and reduction *** study provides inspiring implications to develop high-efficient S-scheme photocatalytic systems for versatile applications in solarenergy conversion.

关键词： Cu 2 WS 4 /MoS 2 S-scheme Heterojunction Photocatalysis

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Two Indium(III)-based Fluorescent Metal-Organic Frameworks for Highly Sensing Fe^(3+),2,4-DNP,and TNP

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Chemical Research in Chinese Universities 2024年第1期40卷 119-126页

作者： WANG Dan LI Wen LI Guanghua HUA Jia LIU Yunling State Key Laboratory of Inorganic Synthesis&Preparative Chemistry Jilin UniversityChangchun130012P.R.China

Two novel metal-organic frameworks(MOFs),JLU-MOF130([In(NH2−BDC)(Imi)(1H−Imi)]·DMF·H2O,NH2−H2BDC=2-aminobenzene-1,4-dicarboxylic acid,1H−Imi=1H-imidazole,DMF=N,N-dimethylformamide)and JLU-MOF131([In(1,4-NDC)(Imi)(1H−Imi)]·DMF0.5,1,4-H_(2)NDC=1,4-naphthalene-dicarboxylic acid),were ***-MOF130 features a three-dimensional(3D)architecture with a neb ***-MOF131 is characterized by a two-dimensional(2D)structure with an sql ***-MOF130 has excellent fluorescence detection performance towards Fe^(3+),2,4-dinitrophenol(2,4-DNP),and 2,4,6-trinitrophenol(TNP),but the fluorescence detection performance of JLU-MOF131 is further improved by converting NH2−H2BDC to more conjugated 1,4-H_(2)*** Stern-Volmer(SV)quenching constant(KSV)values of JLU-MOF130 sensing 2,4-DNP,TNP,and Fe^(3+)are 5.24×10^(4),4.44×10^(4),and 4.73×10^(3) L/mol,*** corresponding limit of detection(LOD)values are 1.17,1.36,and 14.59µmol/*** KSV values for JLU-MOF131 are 1.26×10^(5),9.02×10^(4),and 8.48×103 L/mol,and the corresponding LOD values are 0.35,0.42,and 3.60µmol/L,***,the emission wavelengths of the two MOFs obviously shift as the fluorescence emission intensities decrease upon the addition of 2,4-DNP and TNP,which can be applied in selective detection.

关键词： Metal-organic framework Fluorescence quenching Fe^(3+) 2 4-Dinitrophenol(2 4-DNP) 2 4 6-Trinitrophenol(TNP)

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Advanced oxidation via the synergy of C-defective/C-O band modified ultrathin porous g-C3N4 and PMS for efficient photothermal degradation of bisphenol pollutants and lignin derivatives

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Green Energy & Environment 2024年第7期9卷 1159-1170页

作者： Liquan Jing Meng Xie Yuanguo Xu Chun Tong Xia Du Heng Zhao Na Zhong Huaming Li Jinguang Hu School of Chemistry and Chemical Engineering Jiangsu University Department of Chemical and Petroleum Engineering University of Calgary School of Pharmacy Jiangsu University School of Material Science & Chemical Engineering Harbin University of Science and Technology Institute for Energy Research Jiangsu University

This work uses thermal polymerization of urea nitrate, oxyacetic acid and urea as the raw material to prepare ultra-thin porous carbon nitride with carbon defects and C-O band（OA-UN-CN）. Density functional theory（DFT） calculations showed OA-UN-CN had narrower band gap,faster electron transport and a new internal construction electric field. Additionally, the prepared OA-UN-CN significantly enhanced photocatalytic activation of peroxymonosulfate（PMS） due to enhanced light absorption performance and faster electron overflow. As the result, the OA-UN-CN/PMS could entirely degrade bisphenol A（BPA） within 30 min, where the photodegradation rate was 81.8 and 7.9 times higher than that of g-C3N4and OA-UN-CN, respectively. Beyond, the OA-UN-CN/PMS could likewise degrade other bisphenol pollutants and sodium lignosulfonate efficiently. We suggested possible photocatalytic degradation pathways accordingly and explored the toxicity of its degradation products. This work provides a new idea on the development of advanced photocatalytic oxidation processes for the treatment of bisphenol pollutants and lignin derivatives, via a metal-free photothermal-catalyst.

关键词： Photothermal-catalytic G-C 3 N 4 Peroxymonosulfate Bisphenol Sodium lignosulfonate

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Ru基负载型催化剂对2,2,4,4-四甲基-1,3-环丁二酮加氢效果的影响

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石油化工 2024年第3期53卷 314-322页

作者：柳艳青王贤山杨金生靳海波周昕马磊正和集团股份有限公司技术研发中心山东东营257342 北京石油化工学院新材料与化学工程学院燃料清洁化及高效催化减排技术北京市重点实验室北京102627

以γ-Al_(2)O_(3)为载体、贵金属Ru为活性组分,制备了Ru基单金属催化剂Ru/Al_(2)O_(3),并以2,2,4,4-四甲基-1,3-环丁二酮(TMCB)为原料,在高压反应釜加氢反应评价装置上进行催化加氢合成2,2,4,4-四甲基-1,3-环丁二醇(CBDO)的工艺研究,并... 详细信息

以γ-Al_(2)O_(3)为载体、贵金属Ru为活性组分,制备了Ru基单金属催化剂Ru/Al_(2)O_(3),并以2,2,4,4-四甲基-1,3-环丁二酮(TMCB)为原料,在高压反应釜加氢反应评价装置上进行催化加氢合成2,2,4,4-四甲基-1,3-环丁二醇(CBDO)的工艺研究,并考察了相关工艺条件对加氢反应TMCB转化率和CBDO选择性的影响。实验结果表明,适宜反应条件为反应温度120℃、反应时间2 h、H_(2)压力4 MPa,在此条件下,TMCB的转化率为100%,CBDO的选择性为70.4%,顺反异构比为1.03。

关键词： 2 2 4 4-四甲基-1 3-环丁二酮 2 2 4 4-四甲基-1 3-环丁二醇钌基催化剂加氢反应

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应用量子化学反应性指数分析4,4-二苯丁腈的合成

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比较化学 2024年第1期8卷 1-11页

作者：李彤雷滨瑜闵清邵开元胡文祥湖北科技学院药学院湖北咸宁北京神剑天军医学科学研究院京东祥鹄微波化学联合实验室北京

4,4-二苯丁腈是合成H1受体激动剂Histaprodifens的重要原料之一。化学结构虽然简单,但合成它,要么合成方法简单但需要昂贵的原材料,要么原材料虽然便宜但合成条件苛刻。为了改进4,4-二苯丁腈的合成工艺,我们采用较为便宜的原材料,并通... 详细信息

4,4-二苯丁腈是合成H1受体激动剂Histaprodifens的重要原料之一。化学结构虽然简单,但合成它,要么合成方法简单但需要昂贵的原材料,要么原材料虽然便宜但合成条件苛刻。为了改进4,4-二苯丁腈的合成工艺,我们采用较为便宜的原材料,并通过量子化学计算获得反应的化学反应性指数,来研究和探讨反应机制并指导实验操作。本文在传统的用金属钾对二苯甲烷的烷烃基拔氢反应的方法基础上,采用间接法,即以四甲基乙二胺为起始原料,与正丁基锂发生偶合反应,形成四甲基乙二胺锂鎓盐;后再与二苯甲烷反应,形成二苯甲烷锂盐,最后与3-溴丙腈反应,完成4,4-二苯丁腈的制备。实验表明,该反应条件温和,原料易得,成本低且对环境较友好,反应总收率可达80%左右;实验表明,采用量子化学反应性指数可以分析反应的全过程,并成功地指导化学反应的操作过程。

关键词： 4 4-二苯丁腈量子化学反应性指数合成

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生脉饮复合依托咪酯预处理对肺缺血再灌注损伤大鼠的保护作用及对TLR4/MyD88/NF-κB信号通路的影响

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中文科技期刊数据库（引文版）医药卫生 2024年第6期 0160-0164页

作者：曲晓峰刘再英夏洪莲王琨李晓涵牡丹江医学院第一临床医学院黑龙江牡丹江157000 牡丹江医学院附属红旗医院麻醉科黑龙江牡丹江157000

缺血再灌注(IR)是引起临床肺移植、创伤和急性肺损伤(ALI)的主要原因之一。IR引起的炎症反应和氧化应激是导致和加重其继发性损伤的重要因素。本研究旨在探究生脉饮复合依托咪酯对肺缺血再灌注损伤(LIRI)的治疗作用及其机制。方法我们... 详细信息

缺血再灌注(IR)是引起临床肺移植、创伤和急性肺损伤(ALI)的主要原因之一。IR引起的炎症反应和氧化应激是导致和加重其继发性损伤的重要因素。本研究旨在探究生脉饮复合依托咪酯对肺缺血再灌注损伤(LIRI)的治疗作用及其机制。方法我们用雄性SD大鼠构建LIRI模型,并给药生脉饮和依托咪酯。通过检测大鼠肺组织损伤和氧化应激相关分子的表达,我们探究了生脉饮和依托咪酯对缺血再灌注后肺组织损伤和氧化应激的影响。此外,我们还研究了TLR4信号通路活性的变化,以阐明生脉饮的作用机制。结果 IR后大鼠肺组织损伤相关指标的表达水平明显上升,而生脉饮和依托咪酯则减轻了这种损伤程度。此外,IR后大鼠肺组织的氧化应激水平明显增加,表现为抗氧化分子SOD含量下降、MDA含量上升,而生脉饮和依托咪酯则提高了大鼠肺组织的抗氧化水平。IR后的肺组织中,TLR4等信号通路的活性明显增加,而生脉饮和依托咪酯则抑制了这些信号通路的活性。结论生脉饮复合依托咪酯预处理可能通过减轻大鼠肺脏病理性损伤、改善肺功能、减轻细胞氧化应激、和抑制TLR4信号通路,从而缓解LIRI。

关键词：生脉饮肺缺血-再灌注损伤炎症反应 Toll样受体 4 超氧化物歧化酶单核细胞趋化蛋白可溶性细胞间黏附分子

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