首页|纳米Ce1-4x(FeAlCoLa)xO2-δ固溶体微观光谱特征及氧化还原性能研究

纳米Ce1-4x(FeAlCoLa)xO2-δ固溶体微观光谱特征及氧化还原性能研究

Microscopic Spectral Characteristics and Redox Properties of Nanosized Ce1-4x(FeAlCoLa)xO2-δ Solid Solutions

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采用水热法合成Fe3+、Al3+、Co2+及La3+共掺杂纳米Ce1-4x(FeAlCoLa)xO2-δ(x=0.00~0.05)固溶体,利用X射线衍射(XRD)、透射电子显微镜(TEM)、扫描电子显微镜(SEM)、紫外吸收光谱(UV)、荧光光谱(PL)、拉曼光谱(Raman)以及与H2的程序升温还原反应(TPR)等方法对固溶体的微观结构、形貌、光谱特征和氧化还原活性进行系统表征及分析.XRD结果表明,Ce1-4x(FeAlCoLa)xO2-δ固溶体均呈CeO2立方萤石结构,当掺杂量增加到x=0.04时,在36.6°处出现了微弱的Co3O4杂相,可以确定掺杂离子在CeO2晶格中的固溶度x<0.04.样品的(111)衍射峰位向高角度偏移,表明掺杂离子引起晶格发生畸变.TEM及SEM结果显示样品为球形纳米颗粒,掺杂离子引起晶面间距变小.紫外吸收光谱表明,与纯CeO2相比,掺杂样品的吸收边逐渐红移,在560~780 nm范围观察到掺杂离子的紫外吸收峰.掺杂引起样品能隙降低,从2.84 eV(纯CeO2)逐渐降低至2.10 eV(x=0.05).其原因可归结为掺杂离子在CeO2的价带和导带之间形成新的杂质能级,允许电子从价带跃迁到较低的杂质能级上,继而降低了跃迁能隙.由于掺杂离子引起晶格内部发生畸变以及氧空位比例增大,阻碍了电子的高能跃迁,也可引起能隙减小.荧光光谱证明,掺杂样品的发射峰强度明显降低.Raman光谱表明,掺杂引起F2g峰位发生偏移,峰强减小,峰宽变大.同时,对应于氧空位峰的相对强度逐渐提高.荧光光谱及Raman光谱均证明掺杂离子引起固溶体晶格畸变程度增加,氧空位浓度提高.H2-TPR测试表明,掺杂可以有效降低CeO2的氧化还原反应温度,提高氧化还原活性,当x=0.03的样品表面还原温度最低,还原峰的面积最大,即氧化还原反应活性最佳,表明样品的氧化还原性能与晶粒尺寸、晶格缺陷及氧空位浓度密切相关.通过以上研究证明,四种离子共掺杂CeO2能够有效修饰微观晶体结构,在较低掺杂浓度下即可显著改善样品的催化活性.
Hydrothermal method was used to synthesize nanosized Fe3+,Al3+,Co2+,and La3+co-doped Cei-4x(FeAlCoLa)xO2-δ(x=0.00~0.05)solid solutions.The solid solutions'microstructure,morphology,spectral characteristics,and redox activities were systematically characterized and analyzed by XRD,TEM,SEM,UV,PL,Raman,and temperature-programmed reduction(TPR)with H2.XRD results showed the Cei-4x(FeAlCoLa)x O2-δ solid solutionsexhibited the CeO2 cubic fluorite structure.A tiny diffraction peak corresponding to the Co3O4 impurity phase at 36.6° was observed when the doped content reached x=0.04,indicating that x=0.04 was the solid solubility of doped ions in the CeO2 lattice.The positions of the(111)diffraction peaks were shifted towards a higher angle,which proved the doped ionsinduced the distortion of the lattice.The TEM and SEM images showed the samples were spherical with high crystallinity,and doping caused lattice contraction.The UV absorption spectra revealed that the doped samples'absorption edges were gradually red-shifted compared to pure CeO2.Extra absorption peaks corresponding to the doped ions were found in the region of 560~780 nm.The band gap energies decreased from 2.84 eV(pure CeO2)to 2.1 eV(x=0.05).The reasoncould be that the doped ions formed new impurity energy levels between the valence and conduction bands,which allowed the electrons to transition from the valence band to the lower impurity energy levels and then lowered the band gap energies.In addition,the distortion of the lattice and increased concentration of oxygen vacancies prevented the electrons from transferring to higher energies,which can also result in the reduction of band gap energies.PL spectra showed that doping significantly reduced the emission peak intensities.Raman spectra demonstrated that the dopingresulted in the shift of the F2g peak,the decrease of peak intensities,and the widening of peaks.Meanwhile,the relative intensities of the peak corresponding to the oxygen vacancies were also observed to be enhanced.Thus,both the PL and Raman spectra proved that doping increased the degree of lattice distortion and the concentration of oxygen vacancies.The H2-TPR test results showed that doping can effectively reduce the redox reaction temperatures and improve the redox activities.The sample doped with x=0.03 possess the lowest surface reduction temperature and the largest peak areas,which meansthis sample exhibited the best redox activities.It can be concluded that the redox performances of the samples were closely related to the grain sizes,lattice defects,and oxygen vacancy concentrations.This study showed that the four ions co-doped with CeO2 could effectively modify the microstructure and improve the samples'catalytic activities at a low doping concentration.

Nanosized Ce1-4x(FeAlCoLa)xO2-δ solid solutionsCo-dopedOxygen vacancyRedox activity

孙世龙、张国芳、束俊、郭瑞华、李一鸣、刘卓承、许剑轶、葛启录

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内蒙古科技大学材料与冶金学院,内蒙古包头 014010

钢铁研究总院功能材料所,北京 100081

纳米Ce1-4x(FeAlCoLa)xO2-δ固溶体 共掺杂 氧空位 氧化还原活性

国家自然科学基金项目国家自然科学基金项目国家自然科学基金项目内蒙古自治区"高等学校青年科技人才发展项目"内蒙古自治区"高等学校青年科技人才发展项目"内蒙古自然科学基金项目内蒙古自然科学基金项目内蒙古自治区直属高校基本科研业务费项目

519620285196103252061036NJYT23007NJYT220642022LHMS050212022MS050182023QNJS033

2024

光谱学与光谱分析
中国光学学会

光谱学与光谱分析

CSTPCD北大核心
影响因子:0.897
ISSN:1000-0593
年,卷(期):2024.44(7)