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CERAMICS INTERNATIONAL · 2026 · IF 6

High electrocaloric effects by designing B-site disorder in high-polar-entropy Pb(Sc0.25In0.25Nb0.25 Ta0.25)O3 ceramics

Fang Yu,Chaohai Li,Dong Yang,Jiayu Li,Xiaodan Cao,Biaolin Peng,Kailiang Ren

The electrocaloric (EC) effect in ferroelectric materials has attracted extensive attention because of its high efficiency and potential applications in chip cooling. In this work, we successfully prepared a Pb(Sc 0.25 Ta 0.25 In 0.25 Nb 0.25 )O 3 (PSINT) ceramic via a solid-state reaction method with high-polar entropy. Next, the prepared ceramics were quenched at 1050 °C for various durations. The grain size of the quenched PSINT samples initially decreased to 0.39 μm and then gradually increased to 0.61 μm with a quenching time of 50 h. X-ray diffraction (XRD) patterns of the PSINT ceramics indicate that the PSINT sample transforms from the tetragonal (pseudo-cubic) to an R-3C rhombohedral phase. The measurements of the electrocaloric effect revealed a significant adiabatic temperature change (Δ T ) of approximately 1.98 K at 60 kV cm −1 and room temperature with a quenching time of 40 h. This value is 0.5 K higher than that of untreated PSINT ceramics. Moreover, the B-site atoms of the PSINT high-polar-entropy ceramics changed from a long-range ordered phase to a disordered phase after quenching. This study provides a new technical approach for room-temperature cooling devices by designing B-site disorder in relaxor ferroelectric ceramics.

✓ 已验证 DOI 高影响因子
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POLYMER DEGRADATION AND STABILITY · 2018 · IF 3.193

Effect of nano-TiO2 immobilized antioxidant on ageing resistance behavior of thermoplastic vulcanizate exposed to UV/O3

Hao Yang,Hui Zhang,Henglun Cheng,Baoqing Shentu

Nano-TiO 2 immobilized antioxidant (TiO 2 -KH550-AG) was prepared to improve the ageing resistance of thermoplastic vulcanizate (TPV) exposed to UV/O 3 . TiO 2 nanoparticles were firstly modified with 3-aminopropyltriethoxysilane (KH550) and then reacted with the antioxidant , 3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionic acid (AG), through the acyl chloride reaction followed by the amidation. FT-IR, XPS and TGA measurements confirmed that the antioxidant (AG) was chemically immobilized onto the nano-TiO 2 surfaces. TPV/TiO 2 -KH550-AG nanocomposites were prepared by melt mixing. SEM observation showed that TiO 2 -KH550-AG was homogeneously dispersed into the matrix of TPV. The UV/O 3 ageing test of the samples was carried out in the environment with constant UV intensity of 1.40 mW/cm 2 and ozone concentration of 100 ± 4 mg/m 3 . The ageing resistance behavior of the TPV/TiO 2 -KH550-AG nanocomposites was evaluated by the changes of surface morphology , mechanical properties and carbonyl index during the UV/O 3 ageing test. It was observed that the TPV/TiO 2 -KH550-AG exhibited high stability during the process of UV/O 3 ageing. The results revealed that the anti-ageing efficiency of TiO 2 -KH550-AG was superior to the mixture of the corresponding AG and modified TiO 2 , owing to the better dispersion and migration resistance of TiO 2 -KH550-AG.

CAS / MDL: 919-30-2
研究领域: 材料科学 · 高分子化学
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ELECTROCHIMICA ACTA · 2018 · IF 5.116

Effective mineralization of anti-epilepsy drug carbamazepine in aqueous solution by simultaneously electro-generated H2O2/O3 process

Bo Yang,Tuo Wei,Ke Xiao,Jianping Deng,Gang Yu,Shubo Deng,Juying Li,Caizhen Zhu,Huabo Duan,Qiongfang Zhuo

A novel electro-generated hydroxyl radical ( OH) technique was constructed to effectively degrade the anti-epilepsy carbamazepine (CBZ) representing typical recalcitrant pharmaceutical only through electrochemical method as an alterative peroxone process. The technique involves simultaneously electro-generated H 2 O 2 using a carbon-polytetrafluoroethylene (C/PTFE) cathode to reduce the injected O 2 and electro-generated O 3 using H 2 O oxidation with a Ti mesh/PbO 2 anode in membrane electrode assembly (MEA). The significant OH formation through the synergetic system of in-situ produced H 2 O 2 and O 3 electrochemically could achieved carbamazepine decomposition and total organic carbon (TOC) removal as compared to electro-generated H 2 O 2 or O 3 alone. The main influential factors including current density and aqueous pH were investigated to reveal their effect on CBZ removal efficiencies. Under optimal parameters, CBZ decomposition and TOC mineralization could be completely accomplished after 10 min and 90 min electrolysis, respectively. According to intermediates distribution (e.g. hydroxylated CBZ, phenolics, and carboxylic acids) identified by HPLC-MS/MS, the degradation pathways were proposed for CBZ removal by the synergetic system of C/PTFE-O 2 and MEA. The above results indicated that this electrochemically synergetic system is a potential technique to further purify the water contaminated by recalcitrant pharmaceuticals.

研究领域: 环境科学 · 药学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2023 · IF 8.6

Simultaneous degradation of antibiotic and removal of phosphate in water by a O3/CaO2 advanced oxidation process

Shijia Pan,Wenxuan Jiang,Lu Tian,Xiang Li,Jiaxin Wang,Yawen Wang,Zhen Li,He Guo

The simultaneous presence of antibiotics and phosphate (P) in wastewater will threaten human health and ecological security. The purpose of this study is to study the simultaneous removal of oxytetracycline (OTC) and P in water by O 3 /CaO 2 advanced oxidation process. With enhancing CaO 2 dosage, the degradation efficiency of OTC first improved and then declined, whereas the removal efficiency of P kept increasing. Increasing the amount of O 3 increased the removal efficiency of OTC, but had little effect on the removal efficiency of P. With 0.80 g/L CaO 2 and 0.50 g/h O 3 , the removal efficiency of OTC and P reached 98.0 % and 90.5 % respectively. The lower OTC concentration was beneficial to OTC degradation and P precipitation. The P concentration has no effect on OTC degradation, but it would affect itself precipitation. Alkaline environment was conducive to OTC degradation and P removal. ·OH, ·O 2 − , 1 O 2 made major contribution to the degradation of OTC, which was verified by ESR technique and free radical capture experiment. During the degradation of OTC and P removal, TOC and COD values decreased, while pH and conductivity showed a downward trend. Based on UV–Vis spectrum, 3D EEMF spectrum and LC-MS analysis, two main degradation pathways of OTC were proposed. Toxicity analysis of intermediates showed that their toxicity was significantly lower than that of OTC. The O 3 /CaO 2 system can be considered as an efficient and prospective method for the simultaneous removal of OTC and P in water.

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Journal of Materials Chemistry A · 2023 ·Vol. 11 ·期 7 ·3454-3463 · IF 11.9

Synchronous generation of green oxidants H2O2 and O3 by using a heterojunction bifunctional ZnO/ZnS@C electrocatalyst

Lei Ding,Jinyan Zhao,Zhikang Bao,Shijie Zhang,Huaijie Shi,Jia Liu,Guoliang Wang,Xiaoge Peng,Xing Zhong,Jianguo Wang

H2O2 and O3 production through electrochemical synthesis is a promising approach to replace anthraquinone processes and corona discharge. However, the simultaneous generation of H2O2 and O3 and the use of their synergistic oxidation to degrade organic contaminants remains a challenge. Herein, heterojunction bifunctional ZnO/ZnS@C electrocatalysts were prepared by a one-step pyrolysis method. ZnO/ZnS@C-750 can achieve 90% selectivity for H2O2 and 11% Faraday efficiency for gaseous O3. The primary contributor to such a performance was exploited to accelerate the electron transfer on the heterogeneous interface and generate more reaction sites. H2O2 and O3 can also be simultaneously generated in the electrolyzer and the synergistic effect of H2O2 and O3 can be utilized to completely degrade organic pollutants, such as phenol and tetracycline. This work provided new insights into the design of the 2e− ORR (oxygen reduction reaction) and EOP (electrochemical ozone production) bifunctional electrocatalysts for pollutant degradation.

CAS / MDL: 9012-76-4 1314-98-3
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ACS Omega · 2023 · IF 4.1

Up-Conversion Luminescence and Temperature Sensing of Er3+/Yb3+ Codoped Y2(1–x %)Lu2x %O3 Solid Solution

Haoyue Hao,MengYao Zhu,Liang Li

In this paper, Er3+/Yb3+ codoped Y2(1–x%)Lu2x %O3 solid solution was prepared through the sol–gel method, and the substitution of Y3+ by Lu3+ ions in Y2O3 was confirmed by X-ray diffraction data. The up-conversion emissions of samples under 980 nm excitation and the relative up-conversion processes are investigated. The emission shapes do not vary with the change in doping concentration due to the unaltered cubic phase. The red-to-green ratio changes from 2.7 to 7.8 and then declines to 4.4 as the doping concentration of Lu3+ increases from 0 to 100. The emission lifetimes of green and red have similar variation: the emission lifetime decreases with doping concentration changing from 0 to 60 and rises as the doping concentration continues to increase. The reason why the emission ratio and lifetime change could be originated to the exacerbation of cross-relaxing process and the change of radiative transition probabilities. The temperature-dependent fluorescence intensity ratio (FIR) shows that all samples can be used in noncontact optical temperature sensing, and the method of local structure distortion can be used to improve sensitivity further. The max sensing sensitivities of FIR based on R538/563 and Rred/green reach 0.011 K–1 (483 K) and 0.21 K–1 (300 K). The results display that Er3+/Yb3+ codoped Y2(1–x %)Lu2x %O3 solid solution can be potential candidates for optical temperature sensing in different temperature ranges.

CAS / MDL: 5949-29-1
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2022 · IF 10.319

Single-phase formation mechanism and dielectric properties of sol-gel-derived Ba(Ti0.2Zr0.2Sn0.2Hf0.2Ce0.2)O3 high-entropy ceramics

Jia Liu,Cuiying Ma,Lianli Wang,Ke Ren,Hongpei Ran,Danni Feng,Huiling Du,Yiguang Wang

Single-phase Ba(Ti 0.2 Zr 0.2 Sn 0.2 Hf 0.2 Ce 0.2 )O 3 (BTZSHC) high-entropy ceramics (HECs) with the perovskite structure were successfully prepared via the sol-gel method. The results reveal that the as-prepared ceramics exhibit a single cubic phase belonging to the P m 3 ¯ m space group. The high entropy is the driving force of the formation of single-phase ceramics. A larger entropy (Δ S mix ) and a negative enthalpy (Δ H mix ) are conducive to the formation of single-phase compounds. Herein, Δ S mix  = 0.323 R mole –1 and Δ H mix  = −43.88 kJ/mol. The sluggish-diffusion effect ensures the thermal stability of high-entropy systems. Dielectric measurements reveal that the as-prepared BTZSHC high-entropy ceramics are relaxor ferroelectrics, and the degree of relaxor ( γ ) is 1.9. The relaxor behavior of the as-prepared ceramics can be ascribed to the relaxation and thermal evolution of their polar units (PUs). The findings of this work provide a theoretical basis and technical support for the preparation of single-phase high-entropy ceramics.

CAS / MDL: 16774-21-3
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

Medium-Entropy perovskites Sr(FeαTiβCoγMnζ)O3-δ as promising cathodes for intermediate temperature solid oxide fuel cell

Leyu Shen,Zhihong Du,Yang Zhang,Xu Dong,Hailei Zhao

Medium-entropy perovskites Sr(Fe α Ti β Co γ Mn ζ )O 3- δ (SFTCM) are investigated as potential cathodes for intermediate temperature solid oxide fuel cell (IT-SOFC). The effects of entropy on crystal structure, thermal expansion coefficients (TEC), electrical conductivity, oxygen surface exchange and bulk diffusion coefficients, electrochemical performance, and long-term stability of SFTCM are systematically investigated. High entropy facilitates the diffusion of oxygen ions but hinders the transmission of electrons. The SFTCM with higher entropy shows a lower TEC, displays suppressed strontium surface segregation, and delivers more stable polarization resistance. Although the catalytic activity towards oxygen reduction reaction was slightly reduced, the maximum power density of the LSGM-supported (250 μm) single cell with SrFe 0.25 Ti 0.25 Co 0.25 Mn 0.25 O 3- δ cathode can still reach 0.85 W cm −2 at 800 °C. All these results suggest that the medium-entropy SFTCM perovskites can be promising cathodes materials for IT-SOFC.

✓ 已验证 产品关联 DOI 高影响因子
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY · 2020 ·Vol. 96 ·期 2 ·431-440 · IF 2.008

Ethanol sensing characteristics of (La,Ba)(Fe,Ti)O3 nanoparticles with impurity phases of BaTiO3 and BaCO3

Cao Ensi,Feng Yibiao,Guo Zhaoqing,Wang Huihui,Song Guoqing,Zhang Yongjia,Hao Wentao,Sun Li,Nie Zhongquan

To further improve the ethanol sensing performance of LaFeO 3 (LFO) nanoparticles, the co-doping of acceptor and donor at La and Fe sites at equal mole amount was designed to increase the oxygen adsorbing ability of the resultant nanoparticles. A series of (La,Ba)(Fe,Ti)O 3 nanoparticles, with the designed mole ratios of Ba/La (Ti/Fe) as 0, 0.25, 0.33, 0.50, and 1.0, were prepared by a citric sol–gel method. XRD confirmed the main phase of orthorhombic LFO, and the impurity phases of cubic BaTiO 3 (BTO) and orthorhombic BaCO 3 . The incorporation of Ba and Ti into the LFO lattice was verified by the increased unit cell volume of LFO upon more doping. TEM, BET, and XPS measurements indicated that the appropriate co-doping of Ba and Ti into the LFO lattice and the simultaneous existence of BTO and BaCO 3 resulted in smaller grain size, larger BET surface area, and thus higher concentration of adsorbed oxygen species than those in the pristine LFO nanoparticle. Among all (La,Ba)(Fe,Ti)O 3 sensors, the sensor based on the (La,Ba)(Fe,Ti)O 3 nanoparticles with the designed Ba/La = 0.50 exhibited the highest gas response and sensitivity toward ethanol at the prime working temperature of 132 °C, which was ascribed to the higher surface oxygen coverage contributed by the synergistic effect of co-doping and impurity phases on the number of surface active sites and oxygen adsorbing ability.

CAS / MDL: 10022-31-8
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MATERIALS RESEARCH BULLETIN · 2023 · IF 5.4

Ozone direct electro-generation/activation peroxymonosulfate (PMS) for the degradation of bisphenol A using Ti/NATO anode

Dongxiu Lu,Ruhui Ma,Yuan Chen,Yuancai Chen

In this study, Ni-doped Ti/SnO 2 -Sb anode (Ti/NATO) was prepared and used for electrocatalytic ozone production and in-situ activated peroxymonosulfate (E-Ti/NATO-PMS) to degrade bisphenol A (BPA). SEM, XRD and XPS results indicated that Ni doping could influence the transformations of Sb 5+ and Sb 3+ ions, which decreased the agglomeration of crystallites and increased the O ads and oxygen vacancy (O v ) concentrations. Ti/NATO 1.0 anodes significantly improved the ozone production via outcompeting of the adsorbed O 2ads over water, and inhibiting the desorption of O 2ads , to obtain the highest O 3 concentration with low onset potential and high oxygen evolution potential. E-Ti/NATO 1.0 -PMS system obtained over 92% BPA degradation within 60 min at 10 mA cm −2 and pH ranging from 4 to 10. Radical scavenging experiments revealed that O 3 in situ generated could directly electro-activate PMS into •O 2 − and 1 O 2 . The E-Ti/NATO 1.0 -PMS process could detoxify the BPA through chain scission, rearrangement and ring opening processes, and exhibited great potentials for application.

研究领域: 环境科学 · 化学工程 · 水处理
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Scientific Reports · 2017 ·Vol. 7 ·期 1 ·1-14 · IF 4.259

Discovery of novel solid solution Ca3Si3−x O3+x N4−2x : Eu2+ phosphors: structural evolution and photoluminescence tuning

Wang Baochen,Liu Yan-gai,Huang Zhaohui,Fang Minghao,Wu Xiaowen

Discovery of novel phosphors is one of the main issues for improving the color rendering index (CRI) and correlated color temperature (CCT) of white light-emitting diodes (w-LEDs). This study mainly presents a systematic research on the synthesis, crystal structure variation and photoluminescence tuning of novel (oxy)nitride solid solution Ca 3 Si 3− x O 3+ x N 4−2 x : Eu 2+ phosphors. XRD refinements show that lattice distortion occurs when x value diverges the optimum one ( x  = 1). The lattice distortion causes a widening of emission spectrum and an increase of Stokes shift (ΔSS), which leads to a bigger thermal quenching. With decrease of x value, the emission spectrum shows an obvious red-shift from 505.2 to 540.8 nm, which is attributed to the crystal field splitting. The enhanced crystal field splitting also broadens the excitation spectrum, making it possible to serve as the phosphor for near ultraviolet (n-UV) LEDs. A 3-phosphor-conversion w-LED lamp was fabricated with the as-prepared phosphor, which exhibits high CRI (Ra = 85.29) and suitable CCT (4903.35 K). All these results indicate that the Ca 3 Si 3− x O 3+ x N 4−2 x : Eu 2+ phosphor can serve as the green phosphor for n-UV w-LEDs, with a tunable spectrum by controlling the crystal structure and morphology.

研究领域: 材料科学 · 光学工程
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SEPARATION AND PURIFICATION TECHNOLOGY · 2018 · IF 3.927

Oxygen vacancy of CeO2 improved efficiency of H2O2/O3 for the degradation of acetic acid in acidic solutions

Yalei Ding,Jiejie Wang,Shanshan Xu,Kun-Yi Andrew Lin,Shaoping Tong

In order to completely mineralization of contaminants, it is necessary to develop new methods which can effectively degrade final products of chemical oxidation. Acetic acid (HAc) has been considered one of the typical end products of chemical oxidation of pollutants and thus chosen as a representative target pollutant in the study. Nano-cerium oxide (CeO 2 ), an environment-friendly rare-earth material, was prepared to catalytic ozonation of HAc in acidic solutions. Experimental results show that the prepared CeO 2 could greatly enhance efficiency of H 2 O 2 /O 3 , and also have good stability and recyclability. The Raman spectra indicate that H 2 O 2 interacts with oxygen vacancies of CeO 2 to form peroxide-like species, which could effectively initiate the decomposition of ozone to produce hydroxyl radicals. A mechanism is proposed to explain the activity of peroxide-like species for the decomposition of ozone. The effects of different parameters such as initial pH value, catalyst dosage, and the concentration of H 2 O 2 are also investigated. The results indicate that the CeO 2 /H 2 O 2 /O 3 may provide a convenient and effective method for degrading refractory organic pollutants in acidic wastewaters.

研究领域: 环境科学 · 催化化学
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