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Mustapha Jouiad

Publications and source records attributed to Mustapha Jouiad.

5 recordsLinked to original sources

Role of Bi3+ ion substitution on the piezocatalytic degradation performance of lead-free BaTi0.89Sn0.11O3 at low vibrational energy

Harnessing low ultrasonic vibration energy to drive piezocatalytic reactions has attracted increasing attention in response to current environmental and energy challenges. In this study, we investigate the effect of heterovalent bismuth doping on the piezocatalytic degradation of Rhodamine B (RhB) under low-power ultrasonic excitation. Bismuth ions (Bi$^{3+}$) were substituted into the lead-free ferroelectric BaTi${0.89}$Sn${0.11}$O$_3$, yielding BTSn11-xBi with x = 0, 0.02, and 0.04. The powders were synthesized by the sol-gel method as submicron cubes. The structural, morphological, optical, and piezocatalytic properties were strongly influenced by the Bi content. Compared with pristine BTSn11 and BTSn11-0.04Bi, the BTSn11-0.02Bi sample exhibited the lowest band gap (3.22 eV), the smallest particle size (283 nm), the highest piezoelectric current (approximately 8 microA cm$^{-2}$), and the lowest coercive field required to obtain piezoresponse force microscopy hysteresis loops. As a result, BTSn11-0.02Bi showed the highest RhB degradation efficiency and the largest apparent kinetic rate constant, confirming its superior piezocatalytic performance. Total organic carbon measurements revealed significant mineralization of RhB. In addition, BTSn11-0.02Bi demonstrated good reusability and stability, maintaining high degradation efficiency over three consecutive cycles. These results highlight the potential of Bi-doped BTSn11 ferroelectric materials, particularly BTSn11-0.02Bi, as efficient piezocatalysts for environmental remediation.

cond-mat.mtrl-sci

Ferroelectric KNbO3 nanoplatelets for thermally driven pyrocatalytic hydrogen evolution and dye degradation

Day- and night-induced thermal cycling offers a promising route for harvesting ambient thermal energy to drive sustainable hydrogen production and pollutant degradation. Pyroelectric materials enable this process by converting temperature fluctuations into surface charges capable of promoting catalytic water splitting and advanced oxidation reactions. In this work, we demonstrate efficient pyrocatalytic hydrogen evolution and Rhodamine B (RhB) degradation using orthorhombic ferroelectric Potassium niobate (KNbO$_3$) nanoplatelets (KN-np). Under thermal cycling between 20 and 50 $^\circ$C, KN-np achieved a hydrogen yield of 680 $μ$mol g$^{-1}$ after 30 thermal cycles, corresponding to an average hydrogen production rate of 22.67 $μ$mol g$^{-1}$ per cycle. In addition, KN-np exhibited excellent pyrocatalytic activity toward RhB degradation, reaching 84% removal after only 16 thermal cycles with an apparent kinetic rate constant of 0.11 cycle$^{-1}$. The remarkable catalytic performance is attributed to the strong spontaneous polarization and excellent pyroelectric properties of the KNbO$_3$ nanoplatelets, which promote efficient charge generation and interfacial redox reactions. These findings highlight the potential of KNbO$_3$ nanostructures as efficient pyrocatalysts for clean hydrogen production and environmental remediation.

cond-mat.mtrl-sci

Magnetoelectric coupling in multiferroic CFO/BCTSn core shell nanofibers elaborated by co-axial electrospinning method

Multiferroic CoFe2O4-Ba0.95Ca0.05Ti0.89Sn0.11O3 core-shell nanofibers (CFO@BCTSn NFs) were synthesized by a sol-gel co-axial electrospinning technique. The scanning electron microscope and transmission electron microscope were used to check nanofibers' core-shell structure/configuration. X-ray diffraction and a high-resolution transmission electron microscope were used to confirm the spinel structure of CFO and the perovskite structure of BCTSn. The magnetic character of the resultant CFO@BCTSn NFs was determined by SQUID magnetometry. The piezoelectricity was verified using piezo-response force microscopy, which revealed an entirely covered ferroelectric shell outline, in accordance with SEM and TEM observations. The magnetoelectric (ME) coefficient was measured as a function of the applied external DC magnetic field. The maximum ME coefficient obtained for the CFO@BCTSn NFs was 346 mV cm-1 Oe-1. The high magnetoelectric coupling suggests that CFO@BCTSn NFs could be a promising candidate for magnetic field sensor and magnetoelectric device applications.

cond-mat.mtrl-sci

Strain engineering of the magnetic anisotropy and magnetic moment in NdFeO3 epitaxial thin films

Strain engineering is a powerful mean for tuning the various functionalities of ABO3 perovskite oxide thin films. Rare-earth orthoferrite RFeO3 materials such as NdFeO3 (NFO) are of prime interest because of their intriguing magnetic properties as well as their technological potential applications especially as thin films. Here, using a large set of complementary and advanced techniques, we show that NFO epitaxial thin films, successfully grown by pulsed laser deposition on (001)-SrTiO3, show a strong magnetic anisotropy below a critical thickness tc of 54 nm, associated with the occurrence of structural modifications related to symmetry and domain pattern changes. By varying the tensile misfit strain through the decrease of film thickness below tc, the amplitudes of in and out-of-plane magnetization can be continuously tuned while their ratio stays constant. Furthermore, different low-temperature magnetic behaviors are evidenced for strained and relaxed films, suggesting that the strain-induced structural state impacts the magnetic phase stability.

cond-mat.mtrl-sci

Anti-polar state in BiFeO3/NdFeO3 superlattices

Antiferroelectrics are promising materials for high energy density capacitors and the search for environmentally-friendly and efficient systems is actively pursued. An elegant strategy to create and design new (anti)ferroic system relies on the use of nanoscale superlattices. We report here the use of such strategy and the fabrication of nanoscale BiFeO3/NdFeO3 superlattices and in depth characterization using high resolution X-ray diffraction and Transmission Electron Microscopy. The structural analysis at atomic scale demonstrates that such superlattices host anti-polar ordering most likely described by an antiferroelectric-like Pbnm symmetry. Temperature dependence of anti-polar state and structural transition further hint that the stability of the anti-polar state is controlled by the BiFeO3 layer thickness within the stacking and, in a more moderate way, by interlayer strain. Discovery of such polar arrangement in superlattices and the possible generalization to the whole rare-earth family pave the way to new platforms for energy storage application as well as nano-electronic devices.

cond-mat.mtrl-sci