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SOLAR ENERGY · 2019 · IF 4.674

Preparation of zinc and cerium or both doped Cu2O photoelectric material via hydrothermal method

Binxia Yuan,Xiaobo Liu,Xiaodong Cai,Xinyi Fang,Jianfeng Liu,Maoliang Wu,Qunzhi Zhu

In the paper, the zinc and cerium or both doped cuprous oxide (Cu 2 O) crystals were successfully synthesized under low temperature by a simple hydrothermal process. The surface morphologies, structure properties, and optical properties of Cu 2 O crystals were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and UV-visible absorption spectroscopy. The morphology of pure Cu 2 O crystals, Zn:Cu 2 O crystals, Ce:Cu 2 O crystals and Zn/Ce:Cu 2 O crystals evolved to irregularly cubic structure, exfoliated octahedron, were regular octahedron, and like-spherical aggregate, respectively. The doping of Cu 2 O crystals not only affected the surface morphologies but also significantly influenced the optoelectronic properties. Compared with undoped cuprous oxide, the doped samples had larger optical band gaps. Finally, the aggregation and diffusion were the most important factors for the morphology evolution of Cu 2 O crystal.

研究领域: 材料科学 · 化学
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Journal of Superconductivity and Novel Magnetism · 2024 · IF 1.6

Effects of Ce Doping on the Structure, Morphology, and Magnetic Properties of M-Type Strontium Ferrite

Pi Siwen,Li Jie,Zhang Yingde,Zhou Weina,Shan Shuo,Zhao Xuan

Ce-substituted M-type Sr 1– x Ce x Fe 12 O 19 ( x  = 0.00–0.08) ferrites were successfully synthesized via the ball milling method, and the sintering temperature at 1200 °C for 2 h. The synthesized materials were characterized by X-ray powder diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), and vibrating sample magnetometry (VSM). The elemental makeup of the samples was characterized by energy-dispersive spectrometry (EDS). The XRD results showed the crystal structure and purity of the samples. The FTIR spectroscopy indicated tetrahedral and octahedral tensile vibrations of M-type strontium ferrite at two characteristic peak bands of 554 and 454 cm −1 . The FESEM showed that Ce doping resulted in fine grains. The EDS indicated that Ce content increased with decreasing Sr concentration but that the concentrations of other elements remained basically unchanged. The mass ratio of Sr:Fe is calculated from EDS results and the measured Sr:Fe mass ratio is quite close to the mass ratio calculated from the reactants used to synthesize each sample. The VSM showed that at a Ce doping of x  = 0.02, the coercivity of the samples reached the maximum, and the coercivity values and the saturation magnetization were 3878.25 Oe and 73.625 emu/g, respectively. And such high thermal stability further determines that Ce-substituted strontium ferrites have infinite potential in application fields (T = 450.2 °C).

研究领域: 材料科学 · 磁学
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Materials · 2024 ·Vol. 17 ·期 18 ·4481 · IF 3.1

Fabrication and Characterization of Ce3+-Doped Lithium Alumino-Silicate Scintillating Glass–Ceramic and Fiber

Yongya Wang,Fanbo Meng,Huiyu Chen,Wenqin Luo,Shunjian Xu,Chunyan Lv

Ce3+-doped lithium alumino-silicate (Li-Al-Si) scintillating glass was prepared using a melting method and crystallized via heat treatment. X-ray diffraction and transmission electron microscopy confirmed the presence of nanocrystals in the materials. Radioluminescence spectra, obtained by X-ray excitation, and luminescence spectra, obtained by 338 nm excitation, showed that the luminescence intensity increased after crystallization. The glass was combined with pure silica as the inner cladding to fabricate a hybrid fiber core using a melt-in-tube technique. The composition of the fiber core was examined using an electron probe microanalyzer. The glass fiber produced strong blue luminescence under UV excitation. After a micro-crystallizing heat treatment of the hybrid fiber at 850 °C in a reducing atmosphere, a Ce3+-doped lithium alumino-silicate glass–ceramic scintillating hybrid fiber was obtained. The nanocrystal structure of the fiber core was examined using micro-Raman spectroscopy. Excitation and luminescence spectra of the hybrid fiber before and after micro-crystallization were measured using microspectrofluorimetry. The results demonstrated that the fiber remained luminous after micro-crystallization. Hence, this work provides a new way to prepare scintillating glass–ceramic hybrid fibers for neutron detection.

CAS / MDL: 1344-28-1 12057-24-8
研究领域: 材料科学 · 光学工程
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Journal of Central South University · 2020 ·Vol. 27 ·期 4 ·1176-1185 · IF 1.249

Preparation of magnetic Fe3O4@Cu/Ce microspheres for efficient catalytic oxidation co-adsorption of arsenic(III)

Jin Lin-feng,Chai Li-yuan,Song Ting-ting,Yang Wei-chun,Wang Hai-ying

Magnetic Fe 3 O 4 @Cu/Ce microspheres were successfully prepared by one-step solvothermal approach and further utilized to remediate toxic arsenic (As(III)) pollution. The effects of Cu/Ce elements co-doping on the crystal structure, catalytic oxidation and adsorption behaviors of magnetic microspheres were researched systematically. The results showed that with the aid of Cu/Ce elements, the grain size reduced, lattice defects increased, and the oxygen vacancies and surface hydroxyl groups were improved. Therefore, Cu/Ce elements endowed magnetic Fe 3 O 4 @Cu/Ce microspheres with excellent As(III) removal performance, whose maximum adsorption capacity reached 139.19 mg/g. The adsorption mechanism mainly involved catalytic oxidant co-adsorption. This research developed a feasible strategy for the preparation of high efficiency magnetic adsorbent to enhance the removal of As(III).

研究领域: 环境科学 · 材料科学
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CERAMICS INTERNATIONAL · 2013 · IF 1.789

Photoluminescence properties of Ca–α-SiAlON:Ce3+ phosphors as function of composition and microstructure

Lin Gan,Zhi-Yong Mao,Yi-Fei Wang,Fang-Fang Xu,Ying-Chun Zhu,Qing Huang,Xue-Jian Liu

Cerium-doped Ca–α-SiAlON phosphors with Ca n −1.5 x Si 12− m − n Al m + n O n N 16− n :Ce x ( m =2 n , 0.8≤ m ≤2.4, and 0.02≤ x ≤0.40) nominal compositions have been synthesized by gas pressure sintering (GPS). The photoluminescence (PL) properties were studied in relation to phase composition, particle morphology , and microstructure. Continuous addition of Ce rare-earth (RE) could enhance the emission intensity of phosphors, which was partially attributed to the formation of increased amount of planar defects where dense doping of Ce ions is achieved. Such enhancement could hold up to x =0.32, above which the emission intensity fell slightly due to the formation of more secondary phases and a surface glassy phase rather than concentration quenching. Finally, possible ways to improve the luminescence properties of Ce-doped α-SiAlON phosphors were discussed through tailoring the composition and microstructure.

CAS / MDL: 1306-38-3 471-34-1
研究领域: 材料科学 · 光学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2025 · IF 5.4

Ce-doped carbon dots enhanced by ionic liquids: A potent corrosion shield for N80 steel in aggressive 1M HCl environment

Fengting Li,Yi Zhou,Zhikun Wang,Wentao Qu,Huiling Su,Miantuo Li,Nannan Cui,Shuangqing Sun,Yu Fu,Songqing Hu

Carbon dots (CDs) have been studied as eco-friendly corrosion inhibitors for metals. However, the mechanisms behind their effectiveness are not fully understood. We developed a cost-effective and environmentally friendly method to synthesize Ce-doped CDs (CeCDs) using urea, ammonium citrate, and cerium nitrate. By optimizing the Ce doping concentration to 200 μg/L, we achieved a high corrosion inhibition efficiency. When tested in 1 M HCl, CeCDs at 200 mg/L showed 80 % inhibition, while ionic liquid-modified CeCDs (IL-CeCDs) demonstrated an even higher efficiency of 95.35 % on N80 steel. Both CeCDs and IL-CeCDs adsorb onto metal surfaces through a combination of physical and chemical interactions, inhibiting corrosion mainly by affecting cathodic reactions. Among different Ce-doped CDs, CeCD3N, which has a single Ce atom doping, exhibited the highest molecular reactivity, allowing it to interact more effectively with the Fe surface. Further analysis revealed that Ce doping reduces the energy gap of CDs, enhancing their reactivity. Molecular dynamics simulations showed that CeCD3N adsorbs more strongly and forms a closer inhibitor film on the Fe surface compared to other Ce-doped CDs, making it an effective corrosion inhibitor.

研究领域: 材料科学 · 腐蚀与防护 · 表面化学
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JOURNAL OF NUCLEAR MATERIALS · 2020 · IF 2.485

Phase and microstructure evolution of 0.2Zr1-xCexO2/Zr1-yCeySiO4 (0 ≤ x + y ≤ 1) ceramics designed to immobilize tetravalent actinides

Yi Ding,Zhengdi Jiang,Tianheng Xiong,Zimei Bai,Dandan Zhao,Hui Dan,Tao Duan

Zircon is important ceramic used widely due to its excellent properties, in particular for nuclear waste immobilization . However, it is difficult to obtain mono-phase zircon with high yield, usually result in double-phase ZrO 2 /ZrSiO 4 ceramics. Herein, Ce-doped double-phase 0.2Zr 1- x Ce x O 2 /Zr 1- y Ce y SiO 4 (0 ≤  x  +  y  ≤ 1) ceramics were fabricated and their phase and microstructure evolution were studied. The results demonstrated that Ce content has great influence on the phase composition and microstructure. The ceramics with 0 ≤ x  +  y  < 0.1 are tetragonal-ZrSiO 4 , monoclinic-ZrO 2 and tetragonal-ZrO 2 phases, with 0.1 ≤ x  +  y  ≤ 0.3 are tetragonal-ZrSiO 4 , monoclinic-ZrO 2 , tetragonal-ZrO 2 and cubic-ZrO 2 phases, with 0.3 < x  +  y  ≤ 0.6 are tetragonal-ZrSiO 4 , tetragonal-ZrO 2 and cubic-ZrO 2 phases, and with 0.6 < x  +  y  ≤ 1 are cubic-ZrO 2 and Ce 2 Si 2 O 7 phases. With increasing Ce-doping content, the ZrSiO 4 retained the tetragonal phase, while ZrO 2 transformed from monoclinic to stable cubic phase. Furthermore, lattice parameters , grain size and compactness increased with increasing Ce content.

CAS / MDL: 1306-38-3 1314-23-4
研究领域: 材料科学 · 核废物处理
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JOURNAL OF NUCLEAR MATERIALS · 2018 · IF 2.447

High-temperature stability of (Gd1−xCex)2Zr2O7+x (x = 0–1) synthesized by spray pyrolysis in air

Xin Wang,Min Xue,Songbai Liu,Kuo Jiang

In this paper, (Gd 1− x Ce x ) 2 Zr 2 O 7+ x immobilized matrices with high cerium (Ce) amount-of-substance fractions (up to 90%) were prepared by sol-spray pyrolysis , and then sintered at 1600 °C in air. XRD results showed that all samples were in a mixture of pyrochlore and fluorite phase, even after sintering at 1600 °C. All the sintered bulks were dense, and the densities were independent of the additive content . The SEM results showed that all samples were chemically homogeneous. There was no segregation in the grain boundary. EDS quantification yielded a mean composition close to the stoichiometric chemical composition.

CAS / MDL: 10294-41-4 19598-90-4
研究领域: 材料科学 · 核废料管理
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2016 · IF 2.76

Synthesis and morphology-dependent antimicrobial activity of cerium doped flower-shaped ZnO crystallites under visible light irradiation

Aiping Hui,Junli Liu,Jianzhong Ma

Cerium doped flower-shaped ZnO crystallites were prepared via a facile microwave-assisted hydrothermal method with zinc nitrate hexahydrate as zinc sources, cerium (III) nitrate nonahydrate as dopant. The obtained samples were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscope (TEM), Brunauer-Emmett-Teller surface area measurement (BET), energy dispersive spectroscopy (EDS) and UV⿿vis diffuse reflectance spectroscopy. Antimicrobial activity of the samples against Candida albicans ( C. albicans ) and Aspergillus flavus ( A. flavus ) was compared with pure ZnO under visible light sources. The results indicated that cerium doped flower-shaped ZnO crystallites had different crystal structure with the increased levels of cerium content. Besides, the band gap of ZnO crystallites decreased and its crystallinity increased with the adding of cerium ion. In particular, increasing levels of the cerium dopant more than 0.8% results in decreased optical band gap (3.06   eV) and enhanced antimicrobial activity against C. albicans (75%) and A. flavus (80%) under visibler light sources.

CAS / MDL: 16774-21-3
研究领域: 材料科学 · 微生物学
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ENVIRONMENTAL RESEARCH · 2025 · IF 7.7

Preparation, adsorption and structure of Ce doped layered manganese ion-sieve based on Li2MnO3 spatial structure

Qian Liu,Li Zhang,Yucheng Liu,Xiaoqiang Zheng,Xuna Liu,Zhongquan Zhong,Liping Wei,Qianqian Zhao,Tingting Yao,Ping Yang

With appropriate cerium (Ce) doping, the layered lithium ion-sieve precursor Li 1.37 Ce 0.001 Mn 1.22 O 3 was synthesized using hydrothermal and solid-phase calcination, which exhibited Li/Mn ratio exceeding 1, indicating a high theoretical adsorption capacity. The incorporation of Ce further stabilized the spatial configuration of the layered ion-sieve and controlled the dissolution loss ratio of manganese (Mn) to approximately 0.55%. At 25 °C, with pH of 9 and initial lithium-containing solution concentration of 100 mg/L, the adsorption capacity can reach around 33 mg/g. Despite the presence of interfering ions, it maintained selective adsorption of lithium (Li). The lithium adsorption process by layered lithium ion-sieve adhered to the Langmuir adsorption isotherm model, while the kinetics of adsorption conformed to pseudo-second-order kinetics. This adsorption process was characterized as spontaneous and endothermic, with higher temperatures and concentrations of lithium solutions facilitating both the adsorption process and capacity. It was found that in simulation analysis, compared to the cubic ion-sieve precursor, Li in the layered structure occupied more spatial points, resulting in a more compact stacking and increased bond energy. It alleviated the dissolution loss of Mn during the pickling process. The proximity of Ce resulted in a reduction of the charge on Mn and Li. An appropriate amount of Ce doping will enhance the valence state of Mn; however, excessive Ce doping led to the depletion of electrons from nearby Mn and Li. During pickling process, the Li surrounding Ce in the precursor were preferentially replaced by hydrogen (H) due to their lower charge.

研究领域: 材料科学 · 环境科学
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Journal of Water Process Engineering · 2020 · IF 3.465

γ-Al2O3 doped with cerium to enhance electron transfer in catalytic ozonation of phenol

Yu Li,Luchao Wu,Yun Wang,Peng Ke,Jie Xu,Baohong Guan

Ozone decomposition into free radicals, which can be facilitated by enhancing electron transfer between ozone and catalyst, is an important segment in catalytic ozonation. We doped cerium uniformly on γ-Al 2 O 3 with an impregnation–calcination method to enhance electron transfer in catalytic ozonation of phenol in aqueous solution. The removal efficiency of phenol is raised from 39.7% by ozonation alone to 46.3% by catalytic ozonation with Ce/Al 2 O 3 in 50 min reaction. A higher Ce 3+ /Ce 4+ ratio in Ce/Al 2 O 3 witnesses a higher electron transfer rate in catalytic ozonation and thus a higher degradation efficiency of phenol, illustrating that the activity of Ce/Al 2 O 3 depends on the valence state of Ce. The electron transfer cycle is formed by the electron donation from Ce 3+ to ozone molecule and the electron acceptance of Ce 4+ from adjacent lattice oxygen. After getting the electron, the ozone molecule is decomposed to generate free radical of ·OH on the surface of Ce/Al 2 O 3 . The continuous flow experiments exhibit a stable and high catalytic activity of Ce/Al 2 O 3 for catalytic ozonation, implying the feasibility in practical application.

研究领域: 环境科学 · 催化材料
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JOURNAL OF RARE EARTHS · 2018 · IF 2.524

Phase relations, microstructure, and valence transition studies on CaZr1–xCexTi2O7 (0.0 ≤ x ≤ 1.0) system

Weimin Li,Faqin Dong,Liang Bian,Hao Zou,Mianxin Song

In this study, Ce-doped zirconolite was synthesized through high-temperature solid-state reaction at 1250 °C in air for 96 h. The crystal phase, microstructure and valence transition were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Phase relations of CaZr 1– x Ce x Ti 2 O 7 systems were determined by XRD analyses and Rietveld refinements . Four different phases are identified, namely zirconolite, perovskite , pyrochlore, and cerianite. The phase transformation (2M-zirconolite → 4M-zirconolite → Ce-pyrochlore) is caused by cations rearrangement as cerium content increases. The solubility limit of cerium ions in CaZr 1– x Ce x Ti 2 O 7 system is estimated to be approximately 0.80. Under sintering air atmosphere, partial reduction of Ce 4+ in Ce 3+ is detected in Ce 3d XPS spectra, and the ratio of Ce 3+ and Ce 4+ significantly decreases as cerium content increases.

研究领域: 材料科学 · 化学
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