Systematic investigation of the influence of magnetic and non-magnetic ion substitutions in BiFeO3 under similar internal chemical pressure

IF 3.2 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Journal of Solid State Chemistry Pub Date : 2024-09-18 DOI:10.1016/j.jssc.2024.125019
Ch. Komala Lakshmi , T. Durga Rao , G. Bhavani , M. Sudhadhar , B. Sattibabu , V. Satya Narayana Murthy , T. Karthik , Saket Asthana
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Abstract

Polycrystalline Bi1-xRxFeO3 (RHo and Y, x = 0.00, 0.05 and 0.10) compounds were prepared to perform a systematic investigation of the role of chemical nature and effect of internal chemical pressure on the structural, microstructural, magnetic, electric, ferroelectric and optical properties of the compounds. Structural analysis revealed that lattice distortions observed in Ho and Y-substituted compounds were not the same. The lattice parameters were larger in the case of the Y-substitution compared to the Ho-substituted counterpart. Scanning electron micrographs confirmed the formation of dense, well-connected grains exhibiting a reduction in size with increasing substitution. The magnetic properties of BiFeO3 were enhanced through the suppression of the spin structure with the substitution. The substitution of magnetic (Ho3+) ions led to an improvement in remanent magnetization and coercive field, whereas the substitution of non-magnetic (Y3+) ions resulted in enhanced maximum magnetization with negligible coercive field at room temperature. The ferroelectric measurements evidenced that both remanent polarization and coercive fields improved in substituted compounds, attributed to a decrease in charge carriers. Furthermore, the Y3+ ion substitution positively influenced ferroelectric properties by reducing leakage currents compared to the Ho3+ ion substitution. The optical absorption measurements indicated a decrease in the energy band gap of BiFeO3 with substitution, implying alterations in the material's optical characteristics. The ac conductivity studies demonstrated a discernible reduction in the conductivity of the substituted compounds. Specifically, Ho-substitution exhibited a more pronounced magnitude in the decline in conductivity relative to Y-substitution. This outcome signifies the potential efficacy of Ho-substitution in exerting control over the insulating characteristics of the compounds.

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系统研究类似内部化学压力下 BiFeO3 中磁性和非磁性离子置换的影响
制备了多晶 Bi1-xRxFeO3(RHo 和 Y,x = 0.00、0.05 和 0.10)化合物,以系统研究化学性质和内部化学压力对化合物的结构、微结构、磁、电、铁电和光学特性的影响。结构分析表明,在 Ho 和 Y 取代化合物中观察到的晶格畸变并不相同。与 Ho 取代的化合物相比,Y 取代的化合物的晶格参数更大。扫描电子显微镜照片证实了致密、连接良好的晶粒的形成,其尺寸随着取代度的增加而减小。通过抑制自旋结构的取代,BiFeO3 的磁性得到了增强。磁性(Ho3+)离子的取代改善了剩磁化和矫顽力场,而非磁性(Y3+)离子的取代则增强了最大磁化,但室温下的矫顽力场可忽略不计。铁电测量结果表明,替代化合物的剩磁极化和矫顽力场均有所改善,这归因于电荷载流子的减少。此外,与取代 Ho3+ 离子相比,取代 Y3+ 离子降低了漏电流,从而对铁电特性产生了积极影响。光吸收测量结果表明,BiFeO3 的能带隙随着取代而减小,这意味着材料的光学特性发生了变化。交流电导率研究表明,取代化合物的电导率明显下降。具体来说,相对于 Y 取代,Ho 取代的导电率下降幅度更大。这一结果表明,Ho 取代在控制化合物的绝缘特性方面具有潜在的功效。
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来源期刊
Journal of Solid State Chemistry
Journal of Solid State Chemistry 化学-无机化学与核化学
CiteScore
6.00
自引率
9.10%
发文量
848
审稿时长
25 days
期刊介绍: Covering major developments in the field of solid state chemistry and related areas such as ceramics and amorphous materials, the Journal of Solid State Chemistry features studies of chemical, structural, thermodynamic, electronic, magnetic, and optical properties and processes in solids.
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