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BiFeO3
JOURNAL OF ENVIRONMENTAL MANAGEMENT · 2025 · IF 8.4

Photochemical remediation of soil co-contaminated with tetracycline and Cr(VI) using S-scheme BiFeO3/Cl-g-C3N4 heterostructure photocatalyst: Performance, microbial community changes and phytotoxicity assessment

Tianrui Xu,Guanghui Wang,Xuewen Zhang,Nansheng Deng

Within the domain of animal husbandry, the misuse of antibiotics in conjunction with elevated levels of heavy metals in feed has led to the contamination of agricultural soils with these metals and antibiotics. In this study, S-scheme heterojunction photocatalyst, BiFeO 3 /Cl-g-C 3 N 4 , was synthesized for the photochemical remediation of tetracycline (TC) and Cr(Ⅵ) in co-contaminated soil, utilizing pyrolysis methods. Following an 8-h photocatalytic reaction, 89.6 % of TC and 75.7 % of Cr(Ⅵ) were effectively removed in soil with the application of BiFeO 3 /Cl-g-C 3 N 4 at a mass ratio of 5 %. The diversity of microbial communities in the remediated soil increased, with a shift in dominant genera from redox bacteria to nutrient bacteria associated with carbon and nitrogen cycling. Moreover, the incorporation of BiFeO 3 /Cl-g-C 3 N 4 in the remediation of soil contamination at depths ranging from 0 to 20 cm resulted in reductions of 40.2 % and 50 % in TC and Cr(Ⅵ) concentrations in subsoil layers, respectively, after 21-days of sunlight irradiation. In comparison to the contaminated group soil, soil from the remediation treatment demonstrated increased growth potential for cabbage and spinach. This work definitely demonstrates that this soil photochemical remediation method based on BiFeO 3 /Cl-g-C 3 N 4 is technologically feasible and has immense potential in the application of remediation of organic pollutants and heavy metals co-contaminated soils.

研究领域: 环境科学 · 光催化 · 土壤修复 · 微生物生态学 · 农业化学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2020 ·Vol. 31 ·期 11 ·8464-8471 · IF 2.22

Structural phase transition, optical bandgap, interband electronic transition, and improved magnetism in bivalent Ca-, Sr-, Pb-, and Ba-doped BiFeO3 ceramics

Si Shufang,Deng Hongmei,Wang Tiantian,Yang Pingxiong,Chu Junhao

Perovskite compounds Bi 0.7 A 0.3 FeO 3−δ (BAFO) (A = Ca, Sr, Pb, and Ba) with improved optical and magnetic properties have been synthesized by solid-state method. The effect of bivalent ions substitution on the phase transition, microstructure, optical, and magnetic properties are investigated in detail. X-ray diffraction and Raman scattering spectra analyses indicate the phase transition from rhombohedral to cubic in doped samples and the coexistence of the two phases in BBFO, inducing strong lattice distortions. A blue shift observed in d–d transitions energies can reveal the decreased internal chemical pressure, thus leading to the slight increase in bandgaps of BSFO, BPFO, and BBFO. While, narrowed bandgap of 1.96 eV can be found in BCFO for the increased tailing of the conduction band edge into the gap. Besides, room-temperature ferromagnetism has been observed in Sr-, Pb-, and Ba-doped samples which can be resulted from the suppression of spiral structure of BFO. These results lay a solid foundation on further exploring the potential abilities of BFO ceramics as multiferroic photovoltaic materials.

研究领域: 材料科学 · 固体物理 · 光电 · 磁学
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ADVANCED FUNCTIONAL MATERIALS · 2017 ·Vol. 27 ·期 12 ·1604037 · IF 12.124

Readdressing of Magnetoelectric Effect in Bulk BiFeO3

Xin Xin Shi,Xiao Qiang Liu,Xiang Ming Chen

After decades of study, BiFeO 3 is still the most promising single-phase multiferroic material due to its large polarization and high operating temperature, drawing much attention. As a typical type-I multiferroic material, the magnetoelectric coupling in BiFeO 3 is deemed to be weak due to the different origins of its ferroelectricity and magnetism. Here, the magnetoelectric effect in bulk BiFeO 3 is readdressed both theoretically and experimentally. Based on the Dzyaloshinsky–Moriya interaction scenario, the magnetoelectric effect in BiFeO 3 is actually strong, with a coupling energy of about 1.25 meV and a magnetism-coupled parasitic polarization comparable to that of the type-II multiferroics. However, such strong magnetoelectric coupling also causes the cycloidal spin structure, which inhibits the observation of linear magnetoelectric coupling in bulk BiFeO 3 . To resolve this contradiction, Sm-substitution is utilized to suppress the magnetoelectric effect and unlocks the weak ferromagnetism. At an optimized composition, such a weak ferromagnetic state can be switched back to the cycloidal state by an electric field, thus realizing electrical control of the magnetism. It has been argued that field-controlled phase transition is a promising path to colossal magnetoelectric effect. It is of pioneering significance for further investigations down this road.

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RSC Advances · 2016 ·Vol. 6 ·期 29 ·24760-24767 · IF 3.289

Hydrogen-treated BiFeO3 nanoparticles with enhanced photoelectrochemical performance

Chao Zhang,Yanhong Li,Mengsha Chu,Nannan Rong,Peng Xiao,Yunhuai Zhang

Enhancing charge separation and collection in semiconducting photoelectrodes is a key issue in the area of photoelectrochemical applications. Herein, we report that the photoelectrochemical performance of BiFeO3 nanoparticles can be significantly enhanced by treatment with hydrogen atmosphere at elevated temperature for different time periods. Compared with pristine BiFeO3 nanoparticles, the hydrogen-treated BiFeO3 nanoparticles showed substantial improvement of intrinsic features from structural, optical and electronic aspects. These hydrogen-treated BiFeO3 nanoparticles exhibit an unexpected red shift, which was attributed to the formation of sub-band-gap states between the conduction and valence bands, resulting from oxygen vacancies due to the hydrogen treatment. However, the highly concentrated defects in BiFeO3 nanoparticles can act as charge annihilation centers, which is not conducive to the separation of photo-generated carriers. The hydrogen-treated BiFeO3 prepared at 300 °C for 15 min exhibited optimal photoelectrochemical performance. More than three times higher photocurrent density was achieved compared with pristine BiFeO3, demonstrating its potential in practical application.

CAS / MDL: 10035-06-0 7782-61-8
研究领域: 材料科学 · 能源科学
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Journal of Materiomics · 2021 · IF 6.425

Electric-field-controlled magnetism due to field-induced transition of Pna21/R3c in Bi1-xGdxFeO3 ceramics

Jing Chen,Nan Su,Xiao Li Zhu,Xiao Qiang Liu,Jin-Xing Zhang,Xiang Ming Chen

BiFeO 3 has been recognized as one of the most important room-temperature single-phase multiferroic materials, but it still suffers from several drawbacks especially the weak magnetoelectric coupling. In the present work, the electric-field-controlled magnetism is achieved in Bi 1-x Gd x FeO 3 system, which involves a field-induced transition of Pna 2 1 / R 3 c at the morphotropic phase boundary region, and the magnetic state is switched between cycloidal state and canted antiferromagnetic state. The electric-field-controlled magnetism becomes reversible with the help of annealing, which is confirmed by magnetic hysteresis loops and the quantitative ratio of the involved phases for the as-sintered, as-poled and as-annealed samples. Compared with the systems of Bi 1-x Nd x FeO 3 and Bi 1-x Sm x FeO 3 , it is easier to tune the symmetry from R 3 c to Pna 2 1 with lower rare earth-content, and the field-induced transition is more apparent and subsequently leads to more significant electric-field-controlled magnetism in a wider composition range.

研究领域: 材料科学 · 物理学
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CERAMICS INTERNATIONAL · 2021 · IF 4.527

Effective strategy for optimizing the leakage current and ferroelectric polarization characteristics of BiFeO3_PVDF-TrFE nanocomposite films

Lingfang Xu,Yu Zhang,Chi Gui,Hanshuo Fang,Ruilong Wang,Haibo Xiao,Shiheng Liang,Changping Yang

BiFeO 3 has been extensively studied as an important single-phase multiferroic material at room temperature in the application fields of energy storage, data storage, spintronics, and electro-magnetic sensors. However, the high leakage current caused by the presence of lattice defects such as vacancies constrains the further development of BiFeO 3 . In this paper, we presented a facile method to overcome the high leakage problem via blending BiFeO 3 nanoparticles into the ferroelectric copolymer PVDF-TrFE matrix and introducing a barrier layer beneath the top Pt dot electrode. The leakage current and ferroelectric characteristics of BiFeO 3 _PVDF-TrFE nanocomposite films were discussed comprehensively. Consequently, compared with the composites without the barrier layer, the leakage current density of the BiFeO 3 _PVDF-TrFE composite films reduced two orders of magnitude after coating a pure copolymer layer. Moreover, the remnant ferroelectric polarization reached ~14 μC cm −2 for a moderate weight content (25 wt%) of BiFeO 3 nanoparticle in the blends, with a remarkably smaller coercive electric field than that of pure PVDF-TrFE films. An electrical conduction blocking mechanism was established to elucidate the optimized electric and ferroelectric properties of nanocomposite films.

CAS / MDL: 10361-44-1 1304-85-4
研究领域: 材料科学 · 电子工程
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ACS Nano · 2025 · IF 16

Atomistic Insights into Topochemical Reactions in the BiFeO3 System

Junjie Ding,Wenjun Lv,Hanwen Wang,Weixiao Lin,Wenjun Cui,Wen Zhao,Gustaaf Van Tendeloo,Xiahan Sang

Room-temperature multiferroic BiFeO3 (BFO) is a promising candidate for next-generation memory and spintronic devices, but its synthesis is hindered by metastability and complex phase evolution pathways. Achieving atomic-scale control over these pathways is critical for unlocking BFO’s functional potential. Here, we integrate atomic-resolution scanning transmission electron microscopy, energy-dispersive X-ray spectroscopy and density functional theory to dissect the BFO formation mechanism using annealed Bi/Fe thin-film model systems. We identified the key intermediate phases: Bi-doped α-Fe2O3 and a metastable Aurivillius phase, Bi2FeO6. Our investigation reveals three distinct reaction pathways governed by topochemical constraints: (1) Bi substitution into α-Fe2O3, forming BFO via cation exchange while retaining the oxygen sublattice; (2) Fe incorporation into Bi2O3, driving the layered Bi2FeO6 growth; and (3) transformation of the existing BFO into Bi2FeO6 through Fe out-diffusion and structural rearrangement at the interfaces. These findings provide an atomistic insight into the BFO formation mechanism, demonstrating how topochemical principles and diffusion dynamics dictate the phase evolution.

CAS / MDL: 7439-89-6 7440-69-9
研究领域: 材料科学 · 凝聚态物理 · 纳米技术 · 固态化学 · 电子器件
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2022 ·Vol. 33 ·期 31 ·24038-24047 · IF 2.779

The enhanced piezoelectricity of 0.7BiFeO3–0.3BaTiO3 by optimizing charge defects through annealing

Yu Tengfei,Jiang Subin,Qiao Yi,Liu Feng,Yang Baojuan,Gao Meizhen

High-performance 0.7Bi 1.02 FeO 3 –0.3BaTiO 3 ceramics are prepared by traditional solid-state method with annealing. The effect of annealing temperature ( T A ) on the piezoelectric properties of ceramics are revealed by studying the crystal structures, ferroelectric properties, and electrical properties of the as-sintered ceramic and ceramics annealed at 600, 700, 800, and 900 °C. Through the analysis, we found that T A has little influence on the morphology and crystal structure of ceramics, all ceramics are two-phase ( R-PC ) coexistence structures. But T A relates to the concentration of charge defects. When annealing at 800 °C, the charge defects in the ceramic are the least. Therefore the best performance ( d 33  = 202 \(\pm\) 3 pC/N, T C  = 496 °C) ceramic is obtained. Our experiments demonstrate that the charge defects induced by annealing temperature are very important to the piezoelectricity of BFO–BTO ceramics.

研究领域: 材料科学 · 电陶瓷 · 固体物理
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International Journal of Minerals Metallurgy and Materials · 2024 ·Vol. 31 ·期 10 ·2263-2273 · IF 5.6

Enhanced ferroelectric and improved leakage of BFO-based thin films through increasing entropy strategy

Lu Dongfei,Xi Guoqiang,Li Hangren,Tu Jie,Liu Xiuqiao,Liu Xudong,Tian Jianjun,Zhang Linxing

BiFeO 3 (BFO) has received considerable attention as a lead-free ferroelectric film due to its large theoretical remnant polarization. However, BFO suffers from a large leakage current, resulting in poor ferroelectric properties. Herein, the sol–gel method was used to deposit a series of BFO-based thin films on fluorine-doped tin oxide substrates, and the effects of the substitution of the elements Co, Cu, Mn ( B -site) and Sm, Eu, La ( A -site) on the crystal structure, ferroelectricity, and leakage current of the BFO-based thin films were investigated. Results confirmed that lattice distortion by X-ray diffraction can be attributed to the substitution of individual elements in the BFO-based films. Sm and Eu substitutions contribute to the lattice distortion in a pseudo-cubic structure, while La is biased toward pseudo-tetragonal. Piezoelectric force microscopy confirmed that reversible switching of ferroelectric domains by nearly 180° can be realized through the prepared films. The ferroelectric hysteresis loops showed that the order for the polarization contribution is as follows: Cu > Co > Mn ( B -site), Sm > La > Eu ( A -site). The current density voltage curves indicated that the order for leakage contribution is as follows: Mn < Cu < Co ( B -site), La < Eu < Sm ( A -site). Scanning electron microscopy showed that the introduction of Cu elements facilitates the formation of dense grains, and the grain size distribution statistics proved that La element promotes the reduction of grain size, leading to the increase of grain boundaries and the reduction of leakage. Finally, a Bi 0.985 Sm 0.045 La 0.03 Fe 0.96 Co 0.02 Cu 0.02 O 3 (SmLa-CoCu) thin film with a qualitative leap in the remnant polarization from 25.5 (Bi 0.985 Sm 0.075 FeO 3 ) to 98.8 µC/cm 2 (SmLa-CoCu) was prepared through the synergistic action of Sm, La, Co, and Cu elements. The leakage current is also drastically reduced from 160 to 8.4 mA/cm 2 at a field strength of 150 kV/cm. Thus, based on the increasing entropy strategy of chemical engineering, this study focuses on enhancing ferroelectricity and decreasing leakage current, providing a promising path for the advancement of ferroelectric devices.

研究领域: 材料科学 · 物理学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2024 ·Vol. 35 ·期 7 ·1-12 · IF 2.8

Relaxation behavior of BF-BT based ceramics and improved energy storage performance under low electric field

Xie Le-Tian,Zhou Xiao-Xiao,Tang Yu-Cheng,Yin Yang,Hao Yijin,Pei Jun,Zhang Bo-Ping

With the increasing demand for portable electronics, power electronics and other devices, energy storage materials with high power density and large energy storage density are becoming more and more important. BiFeO 3 -BaTiO 3 lead-free ferroelectric ceramics are deemed as a potential lead-free energy storage material due to their high spontaneous polarization and high Curie temperature. However, high remanent polarization has become a serious obstacle to its practical application. In this work, 0.67Bi (1- x ) Sm x FeO 3 -0.33BaTiO 3 (BS x F-BT, 0 ≤  x  ≤ 0.10) was prepared by the conventional solid phase sintering method. The phase transforms from rhombohedral to pseudocubic, and the dielectric and electrical data reveal that relaxor ferroelectrics are favorable for achieving the small size polar nanoregions and enhanced relaxation behavior. Due to enhanced relaxation behavior by doping Sm 3+ , the recoverable energy storage density ( W rec ) reaches 1.99 J/cm 3 , and the energy storage efficiency ( η ) is 57% at a low electric field (190 kV/cm), which is higher than the undoped ceramic ( W rec  = 0.272 J/cm 3 and η  = 26%). This work also puts forward the concept of Ergodic relaxor ferroelectrics and Non-ergodic relaxor ferroelectrics to explain the improvement of energy storage performance.

研究领域: 材料科学 · 物理学
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APPLIED SURFACE SCIENCE · 2016 · IF 3.15

Photocatalytic hydrogen production over solid solutions between BiFeO3 and SrTiO3

Lingwei Lu,Meilin Lv,Gang Liu,Xiaoxiang Xu

Constituting solid solutions has been an appealing means to gain control over various physicochemical properties. In this work, we synthesized a series of SrTiO 3 -BiFeO 3 solid solutions and systematically explored their structural, optical and photocatalytic properties. Our results show that all solid solutions crystallize in a primitive cubic structure and their band gap values can be easily tuned by adjusting molar ratios between SrTiO 3 and BiFeO 3 . Photocatalytic hydrogen production under both full range and visible light irradiation is greatly improved after forming solid solutions. The highest hydrogen production rate obtained is ∼180   μmol/h under full range irradiation (λ   ≥   250   nm) and ∼4.2   μmol/h under visible light irradiation (λ   ≥   400   nm), corresponding to apparent quantum efficiency ∼2.28% and ∼0.10%, respectively. The activity is found to be strongly influenced by surface area and light absorption. Theoretical calculation suggests that Fe contributes to the formation of spin-polarized bands in the middle of original band gap and is responsible for the band gap reduction and visible light photocatalytic activity .

研究领域: 材料化学 · 光催化 · 能源材料 · 无机固体化学 · 半导体物理 · 太阳能转化 · 表面科学
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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Superior energy storage properties of BiFeO3 doped NaNbO3 antiferroelectric ceramics

Bingsen Wang,Junjun Wang,Yuxiao Du,Jian Dai,Zhenhao Fan,Wenfeng Yue,Fu Huang,Atilla Evcin,Yasemin Tabak,Limei Zheng,Dawei Wang

NaNbO 3 (NN)-based dielectric ceramics for energy storage have garnered significant interest due to their high saturation polarization, low residual polarization, and superior breakdown strength ( E b ). However, the low recoverable energy storage density ( W rec ) and efficiency ( η ) significantly limited their practical application. Herein, BiFeO 3 (BF) was incorporated into NN to optimize the energy storage performance. The NN-BF ceramics exhibited pronounced antiferroelectric (AFE) relaxor phase, alongside grain size reduction and E b enhancement, which contributed to a significant increase of W rec and η . Specially, the optimum W rec of 4.43 J/cm³ and η of 71.51 % were achieved at the composition of 0.9NN-0.1BF. Besides, stable energy storage performance was maintained over a wide temperature range (20–120 °C). These results highlight the potential of NN-BF relaxor AFE ceramics as promising candidates for high-performance energy storage applications.

研究领域: 材料科学 · 能源存储
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