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ZrO2
APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

Exploring the mechanism of ZrO2 structure features on H2O2 activation in Zr–Fe bimetallic catalyst

Yue Yin,Ruolin Lv,Xiaoyang Li,Lu Lv,Weiming Zhang

Bimetallic Fenton catalyst has attracted widespread attention in refractory organics removal. Herein, we firstly investigated the influence of ZrO 2 structure features on H 2 O 2 activation in Zr-Fe bimetallic catalyst. The results show that the heterojunction structure will be formed after high temperature calcination , which makes the ability of Zr-Fe bimetallic catalyst to activate H 2 O 2 for bisphenol A degradation is 3.1 times higher than that of α-Fe 2 O 3 without Zr doping. Through characterization and density functional theory, it was identified that compared to (1 1 0) interface, the adsorption energy of H 2 O 2 on iron sites at (1 1 0)-(1 0 0) interface reduced by 1.27 kJ mol −1 , while the Fe–O bond length in the stable configuration of Fe-OOH increased by 0.16 Å, which was beneficial to the association and dissociation of H 2 O 2 on iron sites. Besides, the surface -OH of amorphous ZrO 2 in Zr-Fe bimetallic catalyst synthesized under low temperature conditions could promote HO 2 • /O 2 •- formation through the surface electron transfer, accelerating the Fe(III) reduction. In conclusion, this study reveals the influence of environment-friendly ZrO 2 structure features on H 2 O 2 activation, proposes a new insight into strengthening the synergistic effect between bimetals, and provides a reference for the structural optimization of bimetallic catalysts.

研究领域: 环境科学 · 催化化学
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Batteries-Basel · 2022 ·Vol. 8 ·期 9 ·115 · IF 5.938

Constructing Robust Solid Electrolyte Interface via ZrO2 Coating Layer for Hard Carbon Anode in Sodium-Ion Batteries

Yuteng Gong,Chengxin Yu,Yu Li,Ji Qian,Chuan Wu,Ying Bai

Hard carbon (HC) has attracted extensive attention due to its rich material source, environmental non-toxicity, superior sodium storage capacity, and lower sodium storage potential, and is considered most likely to be a commercial anode material for sodium-ion batteries (SIBs). Nevertheless, the limited initial Coulombic efficiency (ICE) of HC is the main bottleneck hindering its practical application. To alleviate this issue, herein, a ZrO2coating was skillfully constructed by using a facile liquid phase coating method. The ZrO2coating can act as a physical barrier to prevent direct contact between the HC surface and the electrolyte, thus effectively reducing irreversible sodium adsorption and inhibiting the continuous decomposition of the electrolyte. Meanwhile, this fresh interface can contribute to the generation of a thinner solid electrolyte interface (SEI) with high ionic conductivity. As a result, the ICE of the ZrO2-coated HC electrode can be optimized up to 79.2% (64.4% for pristine HC). Furthermore, the ZrO2-coated HC electrode delivers outstanding cyclic stability so that the capacity retention rate can reach 82.6% after 2000 cycles at 1 A g−1(55.8% for pristine HC). This work provides a flexible and versatile surface modification method to improve the electrochemical property of HC, and hopefully accelerate the practical application of HC anodes for SIBs.

研究领域: 材料科学 · 电化学
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2020 · IF 4.495

Microstructure and high-temperature oxidation resistance of MoSi2-ZrO2 composite coatings for Niobium substrate

Lu Zhu,Xuanru Ren,Xiaohong Wang,Xueqin Kang,Ruixin Zheng,Peizhong Feng

Spent MoSi 2 heating elements, which worked in the industrial electrical furnace at high temperature, were crushed into powders and reused as coating raw materials. ZrO 2 was added into spent MoSi 2 powders to fabricate MoSi 2 -ZrO 2 coatings on niobium by spark plasma sintering, and the microstructure and oxidation behavior of the coatings at 1500 and 1700 °C were explored. The results showed that cracks exist in MoSi 2 coating while ZrO 2 -containing coatings are crack-free with the formation of (Mo,Nb) 5 Si 3 diffusion layer after SPS, indicating good metallurgical bonding. After oxidation at 1500 °C for 20 h, the lowest mass gain is obtained by MoSi 2 -30ZrO 2 coating. SiO 2 and ZrSiO 4 are formed on the composite coatings at elevated temperature, which improves the high-temperature oxidation resistance. After oxidation at 1700 °C for 60 min, the oxide scale of MoSi 2 -30ZrO 2 coating is dense without any voids or cracks, demonstrating better high-temperature oxidation resistance than that of single MoSi 2 coating.

研究领域: 材料科学 · 高温材料 · 涂层技术
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International Journal of Applied Ceramic Technology · 2020 ·Vol. 17 ·期 5 ·2094-2103 · IF 1.762

Phase stability and microstructure evolution of MgO-ZrO2 and MgO-6YSZ ceramic fibers

Kangkang Yuan,Xiaotong Jin,Xinqiang Wang

In this work, MgO-ZrO 2 and MgO-6YSZ ceramic fibers were prepared with sol-gel method via electrospinning. Polymorph stability and microstructure evolution of zirconia fibers were fully characterized by X-ray diffraction, Raman spectra, X-ray photoelectron spectroscopy, and Scanning electron microscope. The results indicated that tetragonal zirconia for MgO-ZrO 2 was obtained and cubic zirconia could be fully stabilized for MgO-6YSZ with MgO molar fractions varying from 0.1 to 0.5 at 800°C. Monoclinic phase appeared with MgO molar fractions even up to 0.5 for MgO-ZrO 2 system and partially or fully stabilized zirconia could be achieved for MgO-6YSZ at 1000°C and 1200°C. Grain size was gradually decreased with increasing of MgO content at 800°C both for MgO-ZrO 2 and MgO-6YSZ ceramic fibers. The grain size of both systems increased with MgO molar fractions varying from 0.1 to 0.2 and then decreased at higher contents at 1000°C and 1200°C. A discussion on relationship among MgO state and the phase stability and grain size was presented. This work shows surface excess and solid solution of MgO predominantly controlled the phase stability and microstructure evolution of zirconia fibers.

CAS / MDL: 13494-98-9 68441-17-8
研究领域: 材料科学 · 陶瓷材料
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CERAMICS INTERNATIONAL · 2020 · IF 3.83

Fabrication and characterization of novel excellent thermal-protection Gd2Zr2O7/ZrO2 composite ceramic fibers with different proportions of Gd2Zr2O7

Jingwei Chen,Xinqiang Wang

Three kinds of Gd 2 Zr 2 O 7 /ZrO 2 (GZC) composite fibers with different proportions of Gd 2 Zr 2 O 7 were prepared by electrospinning method through changing the amount of Gd 3+ in precursor solutions. The thermal decomposition, crystallization process , high temperature stability and heat-conducting properties of GZC fibers were fully characterized. The results showed that there were three crystalline phases, tetragonal phase ZrO 2 , cubic phase ZrO 2 and defect fluorite phase Gd 2 Zr 2 O 7 in all the GZC fibers. The content of Gd 2 Zr 2 O 7 increased gradually with the increase of Gd 3+ in precursor solutions which led to the gradual slowing down of grain growth rate, the decrease of thermal conductivity and the increase of high temperature stability of the obtained composite fibers. The thermal conductivities of all the GZC fiber sheets were lower than that of 7YSZ fiber sheet. The sheets of all the GZC fibers could keep the high temperature stability up to 1300 °C.

CAS / MDL: 68441-17-8
研究领域: 材料科学 · 无机化学
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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Enhanced visible light photocatalytic activity of g-C3N4 decorated ZrO2-x nanotubes heterostructure for degradation of tetracycline hydrochloride

Qingling Chen,Wulin Yang,Jiajun Zhu,Licai Fu,Deyi Li,Lingping Zhou

Photocatalytic degradation is considered as a promising strategy to address the environmental threat caused by antibiotics abuse. Visible light driven g-C 3 N 4 decorated ZrO 2-x nanotubes heterostructure photocatalysts for antibiotic degradation were successfully synthesized by anodic oxidation and following a thermal vapor deposition method. Compared with pure g-C 3 N 4 or ZrO 2-x nanotubes, the composite photocatalysts exhibited more extended visible light response and higher separation rate of photo-generated electron-holes pairs. The optimized heteroctructure with 7.1 wt.% g-C 3 N 4 exhibited 90.6% degradation of tetracycline hydrochloride (TC-H) under 1 h visible light irradiation. The mainly active species of TC-H degradation were photo-generated h + and O 2 - . The pathway of charge migration in the g-C 3 N 4 /ZrO 2-x NTs system was also studied and a possible photocatalytic mechanism was proposed for TC-H degradation. Constructing the g-C 3 N 4 /ZrO 2-x nanotubes heterostructure is anticipated to be an effective strategy for photocatalytic degradation of antibiotics.

CAS / MDL: 64-75-5
研究领域: 环境科学 · 材料科学
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RSC Advances · 2018 ·Vol. 8 ·期 59 ·34069-34077 · IF 2.936

The deactivation of a ZnO doped ZrO2–SiO2 catalyst in the conversion of ethanol/acetaldehyde to 1,3-butadiene

Minhua Zhang,Xuechao Tan,Tong Zhang,Zheng Han,Haoxi Jiang

A deactivation study on the ethanol/acetaldehyde conversion to 1,3-butadiene over a ZnO promoted ZrO2–SiO2 catalyst prepared by a sol–gel method was performed. The samples were characterized by N2 adsorption–desorption isotherms, scanning electron microscopy (SEM), NH3 temperature programmed desorption (NH3-TPD), X-ray powder diffraction characterization (XRD), thermogravimetric analyses (TGA), Fourier transform infrared resonance (FT-IR), 13C magic-angle spinning nuclear magnetic resonance (13C NMR) and X-ray photoelectron spectroscopy (XPS). The pore structure characteristics and surface acidity of Zn0.5–Zr–Si catalysts were largely decreased with time-on-stream and no crystal structure was formed in the used catalyst, indicating that the deactivation was caused by carbon deposition. Two main types of carbon deposition were formed, namely low-temperature carbon deposition with the oxidation temperature of around 400 °C and high-temperature carbon deposition with the oxidation temperature of 526 °C. The carbon species were mainly composed of graphitized carbon, amorphous carbon, carbon in C–O bonds and carbonyls. The deactivated catalyst could be regenerated by a simple oxidation process in air. Adding a certain amount of water into the feed had a positive effect on reducing the carbon deposition.

CAS / MDL: 75-07-0
研究领域: 催化化学 · 材料科学
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

An efficient PDA/Al2O3 nanosheets reinforced ultra-thin ZrO2 coating with attractive anti-corrosion and deuterium resistance property

Zhongyang Zheng,Heping Li,Fangjian Li,Liyu Zheng,Shenming Yin,Xinyun Wang,Youwei Yan

Two-dimensional materials, impermeable to various mediums, have ignited the great interest in developing multifunction nanocomposite coatings. Even though Al 2 O 3 has excellent thermal and chemical stability, it is hard to obtain Al 2 O 3 nanosheets from their non-lamellar structured bulk counterparts. In this work, we have developed a bottom–up strategy to synthesize several-nanometer thick Al 2 O 3 nanosheets by taking graphene oxide as the templates, and further improved their dispersibility by modifying them with poly-dopamine (PDA). These PDA-modified Al 2 O 3 nanosheets were then successfully integrated into the nanosized ZrO 2 coating to enhance its anti-corrosion and gas permeation reduction properties. With the Al 2 O 3 nanosheets inserted, corrosion resistance and deuterium resistance of the ZrO 2 coating were increased by 1000% and 1557%, respectively, both of which were above two orders of magnitude higher than that of the 321 steel substrate. The significant improvements achieved by Al 2 O 3 nanosheets demonstrate their capacity to effectively block the diffusion of both ions and deuterium atoms. This work not only offers a new platform for fabricating nanosheets from non-lamellar structured materials, but also indicates tremendous potential of Al 2 O 3 nanosheets as a novel filler for developing high-performance functional coatings.

研究领域: 材料科学 · 表面工程 · 纳米技术
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY · 2021 ·Vol. 168 ·期 5 ·052507 · IF 4.316

Graphene and Spherical CeO2-ZrO2 Support Pt Nanoparticles as Anode Catalysts for Direct Methanol Fuel Cells

Qingchun Wang,Zihao Wang,Xiaolong Liang,Shengli An,Changkun Cai,Yuanyuan Liu,Jinxiao Bao,Xiwen Song

Spherical CeO2 and CeO2-ZrO2 solid solutions are prepared using a hydrothermal method, Pt/CeO2-ZrO2/GO and Pt-CeO2/GO catalysts are prepared using graphene as a carrier, and the effects of the addition of a CeO2-ZrO2 solid solution on the electrocatalytic activity, stability and anti-CO poisoning performance of methanol fuel cell anodes are investigated. The catalyst samples are characterized via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and the electrochemical properties of the catalysts are investigated using an electrochemical workstation (IVIUM). The results show that Pt/CeO2-ZrO2/GO has a higher electrocatalytic activity and stability against CO oxidation than Pt-CeO2/GO, Pt/GO and commercial Pt/C catalysts, which is attributed to ZrO2. When Zr4+ is added into the CeO2 lattice, the activity of oxygen in the CeO2 lattice, the oxygen mobility and the oxygen vacancies are increased, the oxygen storage capacity is improved, and the intermediate product of CO is more easily oxidized. This finding indicates that Pt/CeO2-ZrO2/GO is a methanol oxidation anode catalyst with a good catalytic activity, stability and resistance to CO poisoning.

研究领域: 材料科学 · 电化学 · 能源科学
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APPLIED SURFACE SCIENCE · 2022 · IF 7.392

Boosting CO2 hydrogenation efficiency for methanol synthesis over Pd/In2O3/ZrO2 catalysts by crystalline phase effect

Zhuping Li,Yong Men,Shuang Liu,Jinguo Wang,Keye Qin,Dandan Tian,Tianle Shi,Li Zhang,Wei An

The crystalline phases of support have great influence on their surface and structure properties. Therefore, adjusting the crystalline structure of heterogeneous catalysts imposes a significant impact on the catalytic performance. Herein, a suite of Pd/In 2 O 3 /ZrO 2 catalysts with different crystalline phases of ZrO 2 were prepared and evaluated for CO 2 hydrogenation to CH 3 OH using the same amount of metal loading. The activity data showed the distinct superior reactivity of Pd/In 2 O 3 /ZrO 2 catalyst used mixed monoclinic and tetragonal phases ZrO 2 (Mix-ZrO 2 ) as support as compared to respective single phase of monoclinic ZrO 2 (m-ZrO 2 ) and tetragonal ZrO 2 (t-ZrO 2 ). The catalysts are extensively characterized through BET, XRD, HRTEM, UV–vis, H 2 -TPR, CO 2 /H 2 -TPD and XPS. Combining the characterization results and activity data, the superior activity of Pd/In 2 O 3 /Mix-ZrO 2 catalyst can be correlated with large particle size of Pd nanoparticles, the concentration of oxygen vacancies, and the abundant medium basic sites, which were essential for activation of H 2 and inert CO 2 and enhancement of catalytic performance. The best-performing Pd/In 2 O 3 /Mix-ZrO 2 catalyst exhibited a remarkable reactivity with space time yield (STY) of 0.54 g methanol ·h −1 ·g cat −1 at 573 K and 5 MPa, and stability without noticeable deactivation after 100 h of time on stream, demonstrating its potential as catalyst used in CH 3 OH synthesis from CO 2 hydrogenation.

研究领域: 催化化学 · 材料科学 · 能源化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2018 · IF 3.927

An effective and magnetic Fe2O3-ZrO2 catalyst for phenol degradation under neutral pH in the heterogeneous Fenton-like reaction

Pan Gao,Yuan Song,Mengjie Hao,Anna Zhu,Hongwei Yang,Shaoxia Yang

A novel Fe 2 O 3 -ZrO 2 catalyst was prepared by the sol-gel method, and investigated for phenol degradation in the Fenton-like reaction under neutral pH condition. The ZrO 2 addition increased the surface areas of the catalyst. Scanning electron microscopy (SEM) showed that ZrO 2 nano-particle dispersed on the surface of Fe 2 O 3 . X-ray photoelectron spectroscopy (XPS) indicated that the Fe 2+ amount increased with the increase of the Zr content on the surface. The Fe 2 O 3 -ZrO 2 catalyst produced hydroxyl radicals (OH ) and superoxide radicals (O 2 − /HO 2 ), and exhibited good catalytic performance in the reaction. Total phenol conversion and 56% TOC removal were achieved after 210 min under neutral pH at 60 °C in the heterogeneous Fenton-like reaction. In addition, the prepared Fe 2 O 3 -ZrO 2 catalyst had good magnetism.

研究领域: 环境科学 · 催化化学
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

Rheology and printability of the ZrO2@C microsphere paste for the fabrication of ZrC ceramics by direct ink writing

Haibo Ouyang,Wenlu Li,Cuiyan Li,Tianzhan Shen,Leer Bao,Sirui Wu

ZrO 2 @C spherical powder was synthesized via a solvothermal method and utilized in the fabrication of ZrC ceramics through direct ink writing (DIW) to enhance rheological properties and reduce sintering temperature. The effects of solid content on the rheological behavior and printability of the ZrO 2 @C paste were systematically investigated. The ZrO 2 @C paste exhibited typical pseudoplastic fluid characteristics and viscoelastic properties, demonstrating excellent shape retention and shear-thinning behavior. Optimal solid content and printing speed were determined to be 54 wt% and 100 mm/s, respectively, leading to superior printability. Using these optimized parameters, green bodies with planar and lattice structures were rapidly and precisely fabricated. After reactive sintering at 1600 °C, the resulting ZrC ceramic achieved a promising bending strength of 30.9 MPa. This study provides a robust strategy for the rapid fabrication of ultrahigh-temperature ceramics with complex geometries.

CAS / MDL: 10026-11-6
研究领域: 材料科学 · 陶瓷工程
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