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Bi2O3
JOURNAL OF MATERIALS PROCESSING TECHNOLOGY · 2018 · IF 3.647

Formation of a highly conductive thick film by low-temperature sintering of silver paste containing a Bi2O3-B2O3-ZnO glass frit

Wanchun Yang,Qin Sun,Qing Lei,Wenbo Zhu,Yufeng Li,Jun Wei,Mingyu Li

A new Pb-free Ag paste containing a Bi 2 O 3 -B 2 O 3 -ZnO glass frit was developed for Al 2 O 3 substrate metallization . First, Bi 2 O 3 -B 2 O 3 -ZnO glass frits with various compositions and glass transition temperatures (T g ) of 322 °C–440 °C were synthesized by using a traditional melt-quenching method. Then, silver pastes containing different contents of the glass frit were sintered on an Al 2 O 3 substrate at temperatures ranging from 450 °C to 600 °C. The glass frit content and the sintering temperature had significant impacts on the electrical resistivity and shear strength of the product. The experimental results indicated that the silver film formed from the paste containing 7 wt.% glass frit and sintered at 600 °C for 15 min had a low electrical resistivity of 2.5 μΩ cm and a high strength of 28.5 MPa. These properties resulted from the formation of a stable glass network that supported the Ag network. Furthermore, ZnAl 2 O 4 was observed to form close to the interface of the Al 2 O 3 substrate, which could improve the shear strength . Moreover, the Bi-based glass frit could be a suitable substitute for Pb-based glass frits in the preparation of environmentally friendly silver pastes for forming thick Ag films on Al 2 O 3 substrates.

研究领域: 材料科学 · 电子材料 · 陶瓷与复合材料 · 烧结技术
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CERAMICS INTERNATIONAL · 2023 · IF 5.2

Effect of Li2CO3–Bi2O3 doping on the low-temperature sintering, structure, and dielectric and mechanical properties of MgO–TiO2(w) ceramics

Qi Yuan,Sen Wang,Gaobin Liu,Kuoming Song,He Zhao,Shuai Yan,Xin Li

Dense MgO–12% TiO 2 (w) ceramics containing 12 wt% TiO 2 , which were doped with Li 2 CO 3 –Bi 2 O 3 composite sintering aids, were prepared at a low sintering temperature of 950 °C in this study. The effects of sintering additives on the sintering characteristics, phase composition, microstructure, and dielectric and mechanical properties of the ceramic samples were systematically investigated, and the influences of their phase composition and microstructure on the dielectric and mechanical properties were examined. The introduction of sintering aids produced a new Bi 4 Ti 3 O 12 phase in the sample structure, while the residual Bi 2 O 3 mixed with the newly formed Mg 2 TiO 4 and Bi 4 Ti 3 O 12 phases distributed at MgO grain boundaries formed a structure surrounding MgO grains. This structure filled the pores in the ceramic sample, which increased its density and enhanced the mechanical properties. At a Li 2 CO 3 –Bi 2 O 3 content of 15 wt%, the density, flexural strength , and Vickers hardness of the ceramic samples reached their maximum values of 3.4 g/cm 3 , 218.9 MPa, and 778.7 HV, respectively. However, the further increase in the Li 2 CO 3 –Bi 2 O 3 content deteriorated their dielectric properties although the dielectric constant and dielectric loss remained below 13.4 and 2.1 × 10 −3 , respectively. The findings of this work indicate that Li 2 CO 3 –Bi 2 O 3 sintering aids can significantly lower the sintering temperature of MgO–12% TiO 2 (w) ceramics and control their dielectric and mechanical properties through microstructural changes.

CAS / MDL: 554-13-2 1304-76-3
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2022 · IF 4.831

Fabrication of hierarchical β-Bi2O3/AuAg microspheres for sensitive, selective and rapid detection of environment pollutants by surface-enhanced Raman spectroscopy

Kun Ge,Yihong Huang,Hanqiang Zhang

In this paper, we report a novel surface-enhanced Raman spectroscopy (SERS) substrate based on hierarchical β-Bi 2 O 3 /Au 2 Ag 2 microspheres for rapid, sensitive and selective detection of environment pollutants including o -dianisidine ( o -diASD) and Hg 2+ in environmental samples. The sheet-like β-Bi 2 O 3 not only provides large specific surface areas for adsorption of molecules and AuAg, but also emerges as semiconductor matrix with chemical enhancement combined with AuAg with electromagnetic enhancement, making promising SERS activity. Particularly, the β-Bi 2 O 3 /Au 2 Ag 2 shows high SERS performance for 4-mercaptobenzoic acid and TMB with minimum detectable concentration of 0.1 μg/L with enhancement factor of 3.1 × 10 7 and 6.3 × 10 7 , respectively. The density functional theory simulations were further adopted to explain the high SERS activity and selectivity for o -diASD and TMB. Finally, the β-Bi 2 O 3 /Au 2 Ag 2 was applied to direct detection of o -diASD, and indirect detection of Hg 2+ by TMB marking in environmental samples. The linearity range of 0.5–200.0 and 0.2–500.0 μg/L with limit of detection of 0.2 and 0.07 μg/L for o -diASD and Hg 2+ ions can be achieved, respectively. This method provides a novel strategy in designing and fabricating SERS substrates with high performance for rapid, sensitive and accurate analysis of environmental pollutants.

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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2022 · IF 6.364

Microstructure evolution and bonding mechanism of ZrO2 ceramic and Ti-6Al-4V alloy joints brazed by Bi2O3-B2O3-ZnO glass paste

Qin Sun,Ludong Yang,Wanchun Yang,Hongjun Ji,Mingyu Li,Yufeng Li

Ceramics and metal joinings have been widely employed in aerospace, dental implants , and the electronic packaging industry for fabricating multifunctional components. In this study, the 35Bi 2 O 3 -50B 2 O 3 -15ZnO (mol.%) glass has been employed for joining the ZrO 2 ceramic and Ti-6Al-4V alloy. The effect of brazing temperature on the microstructure evolution, mechanical properties , and bonding mechanism of brazed joints has been analyzed. The microstructure of the ZrO 2 /glass/Ti-6Al-4V joints and the content of Bi 4 B 2 O 9 , Bi 2 O 3 and Bi 24 B 2 O 39 precipitated crystals in glass were found to be dependent on the brazing temperature. The reaction product of Bi 4 Ti 3 O 12 was identified in the glass/Ti-6Al-4V interface because of the chemical reaction between the oxidized layer of Ti-6Al-4V alloy and glass. A maximum shear strength as high as 48.8 ± 5.2 MPa was obtained. Our work, thus, demonstrates that the 35Bi 2 O 3 -50B 2 O 3 -15ZnO glass is an effective bonding material for joining ZrO 2 ceramic and Ti-6Al-4V alloy under low temperature in an ambient atmosphere.

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RARE METALS · 2022 ·Vol. 41 ·期 6 ·2094-2107 · IF 6.318

Constructing Z-scheme β-Bi2O3/ZrO2 heterojunctions with 3D mesoporous SiO2 nanospheres for efficient antibiotic remediation via synergistic adsorption and photocatalysis

Xu Chong,Zhou Qin,Huang Wei-Ya,Yang Kai,Zhang Yong-Cai,Liang Tong-Xiang,Liu Zhao-Qing

A series of Z-scheme β-Bi 2 O 3 /ZrO 2 heterojunction composites containing three-dimensional (3D) mesoporous silica nanospheres (MSNs) were synthesized as efficient catalysts for antibiotic remediation. The obtained MSN/β-Bi 2 O 3 /ZrO 2 ternary composites possess novel lamellar cross structure, which is well constructed by β-Bi 2 O 3 nanosheets, 3D MSNs, and ZrO 2 nanoparticles. The optimal sample BZS-2 (Bi: Zr: Si = 1: 0.4: 0.33) shows an adsorptive-photocatalytic removal efficiency of 92.7% towards levofloxacin (LVF) and a total organic carbon (TOC) removal efficiency of 60.0% under simulated solar light irradiation for 100 min. BZS-2 can also remove 90.1% and 91.2% of tetracycline hydrochloride (TC) and oxytetracycline hydrochloride (OTC), respectively, and the maximum adsorption capacity of TC over BZS-2 is almost 10 times that of β-Bi 2 O 3 . The improvement of photocatalytic activity can be mainly attributed to the enhanced visible-light adsorption capacity and more efficient separation of photogenerated electron–hole pairs. A possible Z-scheme photocatalytic mechanism of β-Bi 2 O 3 /ZrO 2 heterojunctions based on valence band offset (Δ E VBO ) and conduction band offset (Δ E CBO ) is proposed. This study provides an efficient way to construct novel mesoporous ternary photocatalyst with increased accessible surface area and active sites for treatment of antibiotics by synergistic adsorption and photocatalysis. Graphical abstract

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Journal of Environmental Chemical Engineering · 2021 · IF 5.909

Fabrication of Z-scheme CuPd/SrTiO3–CuPd–Bi2O3 photocatalyst for converting organic dye containing N and S elements into (NH4)2SO4

Congcong Piao,Yitong Lin,Zhiyu Liu,Liang Chen,Jianhe Tang,Dawei Fang,Jun Wang

ABSTRACT Several novel Z-scheme CuPd/SrTiO 3 –CuPd–Bi 2 O 3 photocatalysts are prepared via chemical reduction and calcination methods to degrade organic dyes containing N and S and convert NO 2 - , NO 3 - and SO 3 2- into (NH 4 ) 2 SO 4 . Sodium borohydride (NaBH 4 ), ascorbic acid (C 6 H 8 O 6 ) and hydrazine hydrate (N 2 H 4 ·H 2 O) are selected as reductants to deposit CuPd alloy nanoparticles on corresponding photocatalyst. The influence of solar light irradiation time on photocatalytic degradation of organic dye and conversion of the generated inorganic ions is studied. The reusability and stability of the prepared photocatalysts are assessed. The results indicate that the Z-scheme CuPd/SrTiO 3 –CuPd–Bi 2 O 3 photocatalyst prepared by using NaBH 4 has best photocatalytic activity, reusability and stability. The capture experiment of active species proves that holes play crucial roles in photocatalytic degradation of organic dyes and conversion of SO 3 2- and electrons are momentous for the conversions of NO 2 - and NO 3 - . A possible mechanism on photocatalytic degradation of organic dyes containing N and S and conversions of NO 2 - , NO 3 - and SO 3 2- into (NH 4 ) 2 SO 4 caused by Z-scheme CuPd/SrTiO 3 –CuPd–Bi 2 O 3 photocatalyst is proposed.

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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 2 ·2146-2157 · IF 2.478

The photocatalytic performance of ternary g-C3N4/Bi2O3/TiO2 heterojunction composite for degradation of organic pollutants under visible and ultraviolet light

Zhong Chengwei,Wei Wei,He Huan,Huangfu Zhuoxi,Wang YiZheng,Yu Jiang

Heterojunction photocatalytic materials have received extensive attention by the researchers. In this work, g-C 3 N 4 /Bi 2 O 3 /TiO 2 (TCB) composites with g-C 3 N 4 as the main body were synthesized via microwave-assisted ball milling and the heat treatment method. The photocatalytic activity was evaluated by the degradation efficiency of rhodamine B (RhB) and methylene blue (MB) under visible or UV light irradiation. TCB with a mass ratio of melamine/TiO 2 /Bi(NO) 3 ·5H 2 O of 30:1:0.25 has the best photocatalytic performance when fabricated at 450 °C in open air, and the degradation efficiency of the as-prepared material to RhB was 48.07% under visible light and 51.18% to MB under UV. The results of morphological structure analysis revealed that there was a flocculent structure on the edge of the g-C 3 N 4 film and the phase of TiO 2 and Bi 2 O 3 changed. The presence of β-Bi 2 O 3 enhanced photocatalytic efficiency of the as-prepared materials. The optical properties analysis confirmed that the structure of the hybrid samples can promote electron–hole pairs separately at multilayer heterogeneous interfaces and the electron can react with O 2 to yield the · \({O}_{2}^{-}\) radical. In summary, the ability of novel spatial structure materials to absorb visible light is enhanced, which are facilitated for photocatalytic activity and have excellent stability. Therefore, the study of ternary heterojunction photocatalytic materials provides a reference for environmental remediation.

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OPTICAL MATERIALS · 2020 · IF 2.779

Controlled synthesis and upconversion luminescence properties of Yb3+/Er3+ co-doped Bi2O3 nanospheres for optical and X-ray computed tomography imaging

Dongxun Chen,Fang Wang,Jianqiang Bi,Weili Wang,Lu Wang,Kangning Sun,Dongqi Tang,Yanjie Liang

Bi 2 O 3 nanospheres co-doped with Yb 3+ /Er 3+ upconverting ions pair have been successfully synthesized via a facile hydrothermal method followed by a heat treatment. The resulting Bi 2 O 3 :Yb 3+ ,Er 3+ nanospheres show a monodisperse spherical morphology with narrow size distribution (~180 nm) and display intense upconversion luminescence under 980 nm laser excitation. It is found that the crystal structure, morphology and upconversion luminescence properties of nanospheres have a direct relationship with the doping concentration of Yb 3+ and the subsequent calcination temperature. These Bi 2 O 3 :Yb 3+ ,Er 3+ nanospheres can be prepared in large quantities and can be easily modified with a layer of biocompatible polyethyleneimine (PEI) molecules. The yielded nanospheres could not only maintain uniform size and morphological characteristics, but also show good water dispersibility and biocompatibility. Remarkably, these Bi 2 O 3 :Yb 3+ ,Er 3+ upconversion nanophosphors could also act as an effective contrast agent for X-ray computed tomography (CT) imaging, which show higher contrast efficacy than commercial iodine-based contrast agent. The proposed facile synthetic route and inexpensive matrix materials pave the way for broad use of these Bi 2 O 3 :Yb 3+ ,Er 3+ nanospheres as ideal dual-mode bioimaging probes in biomedical field.

CAS / MDL: 13476-05-6 7790-69-4
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JOURNAL OF SOLID STATE CHEMISTRY · 2024 · IF 3.2

Direct Z-scheme charge transfer Bi2O3/UiO-66-NH2 heterojunctions for boosted photocatalytic degradation of tetracycline hydrochloride in different water systems

Shipeng Liao,Muhammad Arif,Xingyue Qian,Guangyu He

The development of hybrid heterostructure photocatalysts with enhanced visible light absorption capacity holds significant importance in environmental remediation. However, the challenge persists in exploiting strong visible-light responsive photocatalysts with both high efficiency and stability. Herein, we successfully synthesized a hybrid Z-scheme heterojunction of Bi 2 O 3 and UiO-66-NH 2 (Bi 2 O 3 /UiO-66-NH 2 ) through a simple hydrothermal route. The visible light photocatalytic performance of Z-scheme Bi 2 O 3 /UiO-66-NH 2 heterojunction is systematically evaluated for persistent antibiotic tetracycline hydrochloride (TC-HCl) both in the clean and real water matrix. All heterojunction catalysts exhibit superior photodegradation capabilities compared to pristine Bi 2 O 3 and UiO-66-NH 2 . The optimal ratio of the two components heterojunction (BUN-150), in particular, demonstrates the highest removal efficiencies for TC-HCl (95 %) within a 90-min timeframe. This remarkable photocatalytic performance is credited to the Z-scheme charge transfer occurring at the interface of Bi 2 O 3 and UiO-66-NH 2 in Bi 2 O 3 /UiO-66-NH 2 heterojunction. The active species experiments and electron paramagnetic resonance analyses are conducted to identify the active reactive species during the TC-HCl degradation (·OH, h + , and ·O 2 − ), and a precise photocatalytic degradation mechanism is explained. Additionally, the photodegradation intermediates of TC-HCl are detected using the HPLC-MS analysis to explain the degradation pathways of TC-HCl. This research paves the way for the development of novel Z-scheme Bi 2 O 3 -based heterojunction catalysts for outstanding photocatalytic applications.

CAS / MDL: 64-75-5
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ACS Applied Energy Materials · 2024 · IF 5.4

High-Performance Flexible Asymmetric Supercapacitor Based on Nanostructured MnO2 and Bi2O3 Decorated 3D Carbon Nanotube Sponge in an Aqueous Gel-Electrolyte

Jiaxin Sun,Shengjie Li,Yitan Li,Xiaohua Zhang,Zhaohui Yang

Supercapacitors have been highly demanded as advanced energy storage devices. A major obstacle is that, compared to commercial battery systems, their energy density is relatively low. Here, we report a flexible asymmetric supercapacitor with high energy and power densities composed of nanostructured MnO2 nanospheres and Bi2O3 nanoshells decorated on a 3D interconnected carbon nanotube sponge (CNTS) in a neutral hydrogel-electrolyte. Our CNTS@MnO2 electrode and CNTS@Bi2O3 electrode demonstrate an excellent areal capacitance of 5.54 F·cm–3 and 4.76 F·cm–3, respectively. In 10,000 charge–discharge cycles, they maintain 93% and 80% of their initial capacitance, respectively. A flexible asymmetric supercapacitor composed of the CNTS@MnO2 anode and the CNTS@Bi2O3 cathode (embedded in a Na2SO4 hydrogel-electrolyte) delivers a high energy density up to 37 Wh·kg–1 at a cell voltage of 1.8 V, 7 times higher than that of traditional electrochemical double-layer capacitors (EDLCs). The long-term cyclic stability and robust mechanical stability profit from the flexible conductive skeleton of CNTS and meet the demands of wearable flexible electronics.

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2018 · IF 11.698

In-situ synthesis of direct solid-state dual Z-scheme WO3/g-C3N4/Bi2O3 photocatalyst for the degradation of refractory pollutant

Longbo Jiang,Xingzhong Yuan,Guangming Zeng,Jie Liang,Xiaohong Chen,Hanbo Yu,Hou Wang,Zhibin Wu,Jin Zhang,Ting Xiong

Artificial Z-scheme photocatalyst can not only reduce the recombination of photogeneraged electron–holepairs, but also retain prominent redox ability. In this study, direct solid-state dual Z-scheme WO 3 /g-C 3 N 4 /Bi 2 O 3 photocatalyst was successfully synthesized by one step co-calcination stratage using tungstic acid, melamine and bismuth (III) nitrate pentahydrate as the precursors. Surface, morphological, and structural properties of the resulting materials were comprehensive characterized by XRD, XPS, SEM, TEM, UV–vis diffuse reflection spectroscopy, BET surface areas, photoluminescence and ESR analysis. The WO 3 /g-C 3 N 4 /Bi 2 O 3 composite exhibited superior photocatalytic activities for tetracycline degradation than that of pure g-C 3 N 4 , WO 3 , Bi 2 O 3 and their binary composites under visible light irradiation. The enhanced photocatalytic performance of WO 3 /g-C 3 N 4 /Bi 2 O 3 composite can be ascribed to improved visible light absorption, increased surface area and enhanced separation efficiency of photo-generated electron-hole pairs. In addition, the photocatalyst exhibits high stability and reusability. On the basis of the results, a novel direct solid-state dual Z-scheme photocatalytic mechanism was also proposed.

CAS / MDL: 7783-03-1 64-75-5
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CHEMICAL ENGINEERING JOURNAL · 2018 · IF 6.735

Enhanced degradation of Bisphenol A (BPA) by peroxymonosulfate with Co3O4-Bi2O3 catalyst activation: Effects of pH, inorganic anions, and water matrix

Limin Hu,Guangshan Zhang,Meng Liu,Qiao Wang,Peng Wang

In this study, a novel Co 3 O 4 -Bi 2 O 3 catalyst was synthesized using a microwave-assistant method, and the corresponding characteristics were studied through XRD, SEM, and N 2 adsorption. As a peroxymonosulfate (PMS) activator, the catalytic activity of the synthesized catalyst was evaluated on Bisphenol A (BPA) removal, and the result showed that Co 3 O 4 -Bi 2 O 3 catalyst promoted BPA degradation, where 100% BPA was degraded within 15 min under the condition of [catalyst] = 0.1 g·L −1 and [PMS]/[BPA] molar  = 5. The Co 3 O 4 -Bi 2 O 3 /PMS system presented a good catalytic activity when the solution pH varied from 3.0 to 11.0. Under the different concentrations of various inorganic anions in the Co 3 O 4 -Bi 2 O 3 /PMS system, Cl − showed an inhibited effect at low concentration and a promoted effect at high concentration. CO 3 2− showed a slight inhibited effect, while H 2 PO 4 − showed a considerable inhibited effect. Additionally, both NO 3 − and SO 4 2− showed a negligible effect on BPA removal. For the real water bodies, both the drinking water and tap water showed a slight decrease in degradation efficiency of BPA but a distinctly negative effect on BPA mineralization, which might be contributed to the competition between BPA and indigenous organic matters in the two water matrices for their oxidation by radical species. The quenching experiment was enforced and it was found that both SO 4 − and OH on the surface-bound of catalyst were the main active radicals in this system. Overall, the Co 3 O 4 -Bi 2 O 3 catalyst as a PMS activator is a promising catalyst in PMS activation for sulfate radical-based wastewater treatment.

CAS / MDL: 299-11-6
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