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Towards wafer-scale growth of two-dimensional cerium dioxide single crystal with high dielectric performance

Nano Research 2024年第9期17卷 8592-8599页

作者： Zhuofeng Shi Muhammad Imran Xiaohui Chen Xin Liu Yaqi Zhu Zhaoning Hu Saiyu Bu Jialin Zhang Chunhu Li Xiaodong Zhang Li Lin College of Chemistry and Chemical Engineering Qingdao UniversityQingdao 266000China School of Materials Science and Engineering Peking UniversityBeijing 100871China Center for Nanochemistry Beijing Science and Engineering Center for NanocarbonsBeijing National Laboratory for Molecular ScienceCollege of Chemistry and Molecular EngineeringPeking UniversityBeijing 100871China Key Laboratory of Marine Chemistry Theory and Technology Ministry of EducationCollege of Chemistry and Chemical EngineeringOcean University of ChinaQingdao 266100China

Owing to the atomically thin nature,two-dimensional(2D)oxide materials have been widely reported to exhibit exciting transport and dielectric properties,such as fine gate controllability and ultrahigh carrier mobility,that outperform their bulk ***,unlike the successful synthesis of bulk oxide single crystals,reliable methods for synthesizing large-area single crystal of 2D oxide,that would suppress the negative influence from defective grain boundaries,remain unavailable,especially for nonlayered ***,we report that the lattice symmetry between the substrate and cerium dioxide(CeO_(2))would allow for the aligned nucleation and epitaxial growth of CeO_(2)on sapphire substrates,enabling the wafer-sized growth of CeO_(2)single *** careful tuning of the growth temperature and oxygen flow rate contributed to the harvesting of CeO_(2)wafer with reduced thickness and enhanced growth *** removal of grain boundaries improved the dielectric performance in terms of high dielectric strength(Ebd≈8.8 MV·cm^(-1)),suppressed leakage current,along with high dielectric constants(εr≈24).Our work demonstrates that with fine dielectric performance and ease of synthesizing wafer-sized single crystals,CeO_(2)can function as potential candidate as gate insulator for 2D-materials based nanoelectronics,and we believe the reported protocol of aligned nucleation can be extended to other 2D oxides.

关键词： dielectric materials two-dimensional materials chemical vapor deposition cerium dioxide

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Preparation of cerium dioxide Functionalized Magnetic Layered Double Hydroxides for High-efficiency Phosphopeptide Enrichment

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Chemical Research in Chinese Universities 2023年第2期39卷 253-259页

作者： JIANG Dandan QI Ruixue LYU Siqi WANG Wei LIU Jinghai JIA Qiong College of Chemistry and Materials Science Inner Mongolia Key Laboratory of Carbon NanomaterialsInner Mongolia Minzu UniversityTongliao028000P.R.China College of Chemistry Jilin UniversityChangchun130012P.R.China

In this work,we prepared a material with magnetic nanoparticles(Fe_(3)O_(4))as core,layered double hydroxides(LDHs)as affinity shell,and cerium dioxide(CeO_(2))as functional molecules(denoted as Fe_(3)O_(4)@LDH-CeO_(2)).On the basis of combined immobilized metal ion affinity chromatography(IMAC)and metal oxide affinity chromatography(MOAC),Fe_(3)O_(4)@LDH-CeO_(2) was used to enrich phosphopeptides with high *** material exhibited high selectivity(α-casein:β-casein:BSA=1:1:5000,mass ratio),high recovery(95.87%),and good reusability of 10 times adsorption-desorption *** feasibility of Fe_(3)O_(4)@LDH-CeO_(2) was further investigated by extracting phosphopeptides from biological samples(nonfat milk,serum,saliva,and A549 cell lysate).

关键词： Layered double hydroxide cerium dioxide Magnetic Phosphopeptide enrichment

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cerium dioxide as a new reactive sorbent for fast degradation of parathion methyl and some other organophosphates

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Journal of Rare Earths 2014年第4期32卷 360-370页

作者： Pavel Janos Pavel Kuran Martin Kormunda Vaclav Stengl Tomas Matys Grygar Marek Dosek Martin Stastny Jakub Ederer Vera Pilarova Lubos Vrtoch Faculty of the Environment University of Jan Evangelista Purkyne Faculty of Science University of Jan Evangelista Purkyne Institute of Inorganic Chemistry AS CR v.v.i.

cerium dioxide was used for the first time as reactive sorbent for the degradation of the organophosphate pesticides para-thion methyl, chlorpyrifos, dichlofenthion, fenchlorphos, and prothiofos, as well as of some chemical warfare agents-nerve gases soman and O-ethyl S-[2-（diisopropylamino） ethyl] methylphosphonothioate （VX）. CeO2 specimens were prepared by calcination of basic cerous carbonate obtained by precipitation from an aqueous solution. The CeO2 samples containing certain amounts （1 wt.%-5 wt.%） of the neighboring lanthanides （La, Pr, Nd） were prepared in a similar way from pure lanthanide salts. It was shown that ceria accelerated markedly the decomposition of parathion methyl causing the cleavage of the P-O-aryl bond in the pesticide molecule. A similar reaction mechanism was proposed for the degradation of other organophosphate pesticides and nerve agents. The degradation times （reaction half-times） were in an order of minutes in the presence of CeO2, compared to hours or days under common environ-mental conditions. The reaction in suitable organic solvents allowed conversions of about 90%for parathion methyl loading of 20 mg pesticide/g CeO2 within 2 h with a reactant half-life in the order of 0.1 min. The key parameter governing the degradation efficiency of CeO2 was the temperature during calcination. At optimum calcination temperature （about 773.15 K）, the produced ceria retained a sufficiently high surface area, and attained an optimum degree of crystallinity （related to a number of crystal defects, and thus poten-tial reactive sites）. The presence of other lanthanides somewhat decreased the reaction rate, but this effect was not detrimental and permitted the possible use of chemically impure ceria as a reactive sorbent. A fast organophosphate degradation was demonstrated not only in non-polar solvents （such as heptane）, but also in polar aprotic solvents （acetonitrile, acetone） that are miscible with water. This opens new possibilities for designi

关键词： cerium dioxide carbonate precursor lanthanides organophosphate pesticide parathion methyl chemical warfare agents hydrolysis non-aqueous solvents rare earths

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Inhibition of bromate formation by reduced graphene oxide supported cerium dioxide during ozonation of bromidecontaining water

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Frontiers of Environmental Science & Engineering 2019年第6期13卷 81-89页

作者： Bei Ye Zhuo Chen Xinzheng Li Jianan Liu Qianyuan Wu Cheng Yang Hongying Hu Ronghe Wang Shenzhen Environmental Science and New Energy Technology Engineering Laboratory Tsinghua-Berkeley Shenzhen InstituteTsinghua UniversityShenzhen 518055China Key Laboratory of Microorganism Application and Risk Control of Shenzhen Guangdong Provincial Engineering Research Center for Urban Water Recycling and Environmental SafetyGraduate School at ShenzhenTsinghua UniversityShenzhen 518055China Environmental Simulation and Pollution Control State Key Joint Laboratory State Environmental Protection Key Laboratory of Microorganism Application and Risk Control(SMARC)School of EnvironmentTsinghua UniversityBeijing 100084China Division of Energy and Environment Graduate School at ShenzhenTsinghua UniversityShenzhen 518055China

Ozone(O3)is widely used in drinking water disinfection and wastewater ***,when applied to bromide-containing water,ozone induces the formation of bromate,which is *** previous study found±at graphene oxide(GO)can enhance the degradation efficiency of micropollutants during ***,in this study,GO was found to promote bromate formation during ozonation of bromide-containing waters,with bromate yields from the O3/GO process more than twice those obtained using ozone *** promoted bromate formation was attributed to increased hydroxyl radical production,as confirmed by the significant reduction(almost 75%)in bromate yield after adding t-butanol(TBA).cerium oxide(less tfian 5 mg/L)supported on reduced GO(xCeO2/RGO)significantly inhibited bromate formation during ozonation compared with reduced GO alone,and the optimal Ce atomic percentage(x)was determined to be 0.36%,achieving an inhibition rate of approximately 73%.Fourier transform infrared(FT-IR)spectra indicated the transformation of GO into RGO after hydrothermal treatment,and transmission electron microscope(TEM)results showed that CeO2 nanoparticles were well dispersed on the RGO *** X-ray photoelectron spectroscopy(XPS)spectra results demonstrated that the Ce^3+/Ce^4+ratio in xCeO2/RGO was almost 3-4 times higher than that in pure CeO2,which might be attributed to the charge transfer effect from GO to ***,Ce+on thexCeO2/RGO surface could quench Br-and BrO-to further inhibit bromate ***,0.36CeO2/RGO could also enhance the degradation efficiency of N,N-diethyl-zn-toluamide(DEET)in synthetic and reclaimed water during ozonation.

关键词： Bromate Catalytic ozonation Graphene oxide cerium dioxide

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Enhanced corrosion resistance of epoxy resin coating via addition of CeO_(2) and benzotriazole

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Chinese Journal of Chemical Engineering 2024年第3期67卷 89-96页

作者： Xu Han Ruijie Guo Baolong Niu Hong Yan College of Materials Science and Engineering Taiyuan University of TechnologyTaiyuan 030024China Key Laboratory of Interface Science and Engineering in Advanced Materials Ministry of EducationTaiyuan University of TechnologyTaiyuan 030024China

The use of fillers to enhance the corrosion protection of epoxy resins has been widely *** this work,cerium dioxide(CeO_(2))and benzotriazole(BTA)were introduced into an epoxy resin to enhance the corrosion resistance of Q235 carbon *** electron microscopy results indicated that the CeO_(2) grains were rod-like and ellipsoidal in shape,and the distribution pattern of BTA was analyzed by energy dispersive *** dynamic potential polarization curve proved the excellent corrosion resistance of the composite epoxy resin with CeO_(2) and BTA co-addition,and electrochemical impedance spectroscopy test analysis indicated the significantly enhanced long-term corrosion protection performance of the composite *** the optimal protective performance was provided by the coating containing 0.3%(mass)CeO_(2) and 20%(mass)BTA,which was attributed to the barrier performance of CeO_(2) particles and the chemical barrier effect of *** formation of corrosion products was analyzed using X-ray *** addition,the corrosion resistance mechanism of the coating was also discussed in detail.

关键词： Benzotriazole cerium dioxide Corrosion resistance Carbon steel Epoxy resin coating Preparation

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ROS Balance Autoregulating Core-Shell CeO_(2)@ZIF-8/Au Nanoplatform for Wound Repair

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Nano-Micro Letters 2024年第8期16卷 341-361页

作者： Xi Zhou Quan Zhou Zhaozhi He Yi Xiao Yan Liu Zhuohang Huang Yaoji Sun Jiawei Wang Zhengdong Zhao Xiaozhou Liu Bin Zhou Lei Ren Yu Sun Zhiwei Chen Xingcai Zhang The Higher Educational Key Laboratory for Biomedical Engineering of Fujian Province Research Center of Biomedical Engineering of XiamenDepartment of BiomaterialsCollege of MaterialsXiamen UniversityXiamen 361005People’s Republic of China Department of Electronic Science Fujian Provincial Key Laboratory of Plasma and Magnetic Resonance ResearchSchool of Electronic Science and EngineeringXiamen UniversityXiamen 361005People’s Republic of China John A Paulson School of Engineering and Applied Sciences Harvard UniversityCambridgeMA 02138USA Department of Otorhinolaryngology Union Hospital of Tongji Medical CollegeHuazhong University of Science and TechnologyWuhan 430022People’s Republic of China NO.1 Middle School Affiliated to Central China Normal University Wuhan 430223People’s Republic of China

Reactive oxygen species(ROS)plays important roles in living *** ROS is a double-edged sword,which can eliminate drug-resistant bacteria,but excessive levels can cause oxidative damage to cells.A core–shell nanozyme,Ce O_(2)@ZIF-8/Au,has been crafted,spontaneously activating both ROS generating and scavenging functions,achieving the multifaceted functions of eliminating bacteria,reducing inflammation,and promoting wound *** Au Nanoparticles(NPs)on the shell exhibit high-efficiency peroxidase-like activity,producing ROS to kill ***,the encapsulation of Ce O_(2) core within ZIF-8 provides a seal for temporarily limiting the superoxide dismutase and catalase-like activities of Ce O_(2) ***,as the ZIF-8 structure decomposes in the acidic microenvironment,the Ce O_(2) core is gradually released,exerting its ROS scavenging activity to eliminate excess ROS produced by the Au *** two functions automatically and continuously regulate the balance of ROS levels,ultimately achieving the function of killing bacteria,reducing inflammation,and promoting wound *** innovative ROS spontaneous regulators hold immense potential for revolutionizing the field of antibacterial agents and therapies.

关键词： Metal-organic framework(MOF) Reactive oxygen species(ROS) cerium dioxide Au nanoparticles Wound healing

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CeO_(2)-clay composites for ultra-long cycle life electrochemical capacitive energy storage application

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Journal of Rare Earths 2023年第5期41卷 728-739,I0004页

作者： Shan-Shan Chai Wei-Bin Zhang Jing-Lei Yang Lun Zhang Xiong-Wei Han Myat Myintzu Theint Xue-Jing Ma College of Materials and Chemistry&Chemical Engineering Chengdu University of TechnologyChengdu 610059China Mineral Development Section for the International Relation Department of MinesMinistry of Natural Resources and Environmental ConversationNay Pyi Taw15011Myanmar

The lattice expansion caused by the reduction of Ce(Ⅳ)to Ce(Ⅲ)impeded the development of the CeO_(2)as an effective electrode material for electrochemical ***,we prepared CeO_(2)-clay composites through a one-step hydrothermal *** interlayer structures of clays efficiently accommodate volume changes induced by crystal lattice expansion to achieve ultra-long cycle *** 60000 charge-discharge cycles,the capacitance retention rate of the assembled asymmetric supercapacitors is as high as~-100%.The key findings of this work reveal the potential application of clays in achieving ultralong cycle stability of the CeO_(2)electrode material,paving the way for further application of the CeO_(2)in electrochemical energy storage.

关键词： cerium dioxide Clay mineral Cycle life Electrochemical supercapacitor Rareearths

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In-situ TEM study on the evolution of dislocation loops and bubbles in CeO_(2)during Kr^(+)single-beam and Kr^(+)-H_(2)^(+)dual-beam synergetic irradiation

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Journal of Materials Science & Technology 2022年第28期123卷 49-59页

作者： Ziqi Cao Guang Ran Zhen Wang Yipeng Li Xiaoyong Wu Lu Wu Xiuyin Huang Huajun Mo College of Energy Xiamen UniversityXiamen 361102China The First Sub-Institute Nuclear Power Institute of ChinaChengdu 610041China Fujian Provincial Nuclear Energy Engineering Technology Research Center Xiamen 361102China

CeO_(2)is widely used as the nonradioactive surrogate fuel of UO_(2)when studying the irradiation performance of UO_(2).The evolution and characteristics of dislocation loops and bubbles in CeO_(2)foils were studied by in-situ transmission electron microscopy(TEM)observation during 400 ke V Kr^(+)&30 ke V H_(2)^(+)dual-beam synergetic irradiation and 400 ke V Kr^(+)single-beam irradiation at 1073 *** rotation of the habit plane of dislocation loops induced by above ion irradiation was found in the CeO_(2)for the first time,such as from[211]to[311]and then to[100].The rafted loops were first observed under Kr^(+)&H_(2)^(+)dual-beam synergetic irradiation,which not only had similar[111]direction,but also belonged to perfect dislocation loops(PDLs).The rafted loops were formed not only by the growth of loops that absorbed irradiation defects,but also by the combination of ***,this phenomenon of loop rafting was not obvious during Kr single-beam *** was first found that Kr^(+)irradiation induced the change of Burgers vectors of *** absorption of large PDLs to small PDLs was also *** average size and areal number density of dislocation loops and gas bubbles as a function of irradiation dose were constructed,which showed that the addition of H_(2)^(+)obviously affected the characteristics of dislocation loops and gas bubbles and the swelling of CeO_(2).

关键词： Nuclear Fuel cerium dioxide In-situ TEM Irradiation Dislocation Bubbles

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Enhancing low-temperature NH_(3)-SCR performance of Fe-Mn/CeO_(2)catalyst by Al_(2)O_(3)modification

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Journal of Rare Earths 2022年第9期40卷 1454-1461,I0005页

作者： Lulu Li Jiawei Ji Wei Tan Wang Song Xin Wang Xiaoqian Wei Kai Guo Wanyu Zhang Changjin Tang Lin Dong School of Environmental and Chemical Engineering Jiangsu University of Science and TechnologyZhenjiang 212003China School of Chemistry and Chemical Engineering Nanjing UniversityNanjing 210093China Jiangsu Key Laboratory of Vehicle Emissions Control School of EnvironmentCenter of Modern AnalysisNanjing UniversityNanjing 210093China School of Environment Nanjing Normal UniversityNanjing 210093China

In the work,supported catalysts of FeO_(x) and MnO_(x) co-supported on aluminum-modified CeO_(2)was synthesized for low-temperature NH_(3)-selective catalytic reduction(NH_(3)-SCR)of ***,the SCR activity of the obtained catalyst is markedly influenced by the adding amount of Al and the appropriate Ce/Al molar ratio is 1/*** activity tests demonstrate that Fe-Mn/Ce1 Al2 catalyst shows over 90%NO conversion at 75-250℃and exhibits better SO_(2)resistance compared to Fe-Mn/CeO_(2).Fe-Mn/Ce1 Al2 shows the expected physicochemical characters of the ideal catalyst including the larger surface and increased active reaction active sites by controlling the amount of Al ***,the better catalytic activity is well correlated with the present advantaged surface adsorption oxygen species,Mn^(4+)species,Ce^(3+)species and the enhanced reducibility of Fe-Mn/Ce1 Al2,which is superior to the Fe-Mn/CeO_(2)*** importantly,we further demonstrate that the amount and strength of surface acid sites are improved by Al-doping and more active intermediates(monodentate nitrate)is generated during NH_(3)-SCR *** work provides certain insight into the rational creation of simple and practical denitration catalyst environmental purification.

关键词： Selectivity catalytic reduction NO removal Low-temperature activity Al doping cerium dioxide Rare earths

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Integrating ceria with cobalt sulfide as high-performance electrocatalysts for overall water splitting

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Fundamental Research 2023年第3期3卷 356-361页

作者： Huilin Wang Xiaoxiao Han Lingling Zhang Ke Wang Rui Zhang Xiao Wang Shuyan Song Hongjie Zhang a State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchun 130022China School of Applied Chemistry and Engineering University of Science and Technology of ChinaHefei 230026China Department of Chemistry Tsinghua UniversityBeijing 100084China

The development of bifunctional electrocatalysts for overall water splitting is highly desired for converting electricity into chemical ***,the synthesis of high-performance bifunctional electrocatalysts remains a pressing ***,we found that both the oxygen evolution reaction(OER)and hydrogen evolution reaction(HER)performance of the Co_(3)S_(4) electrode can be significantly improved by integration with CeO_(2).Specifically,as-prepared 5%Ce-Co_(3)S_(4) and 1%Ce-Co_(3)S_(4) delivered low overpotentials of 290 and 257 mV to achieve 10 mA cm^(-2) for the OER and HER in 1.0 M KOH,*** crucial role of CeO_(2) originated from its unique surface with abundant oxygen vacancies,which were beneficial for the stabilization of Co^(2+)sites with high OER activity and both the adsorption and dissociation of water molecules in the HER *** work is expected to provide a general approach to prepare a wide range of high-performance electrode materials for energy-related applications.

关键词： Cobalt sulfide cerium dioxide Overall water splitting Oxygen evolution reaction Hydrogen evolution reaction

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