无机材料学报

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高熵稀土氧化物添加对BaO-CaO-Al2O3-B2O3-SiO2封接玻璃结构与长期高温稳定影响

程振乾1,2, 石正南3, 张标1, 刘洋2, 孙略升2, 林慧兴3, 叶枫*1,*, 任海深*3,*   

  1. 1.哈尔滨工业大学 材料科学与工程学院,哈尔滨 150001;
    2.中国电子科技集团公司第四十九研究所,哈尔滨 150028;
    3.中国科学院 上海硅酸盐研究所,上海 201899
  • 收稿日期:2026-05-08 修回日期:2026-07-05
  • 作者简介:程振乾(1985-), 男, 博士研究生. E-mail: chengzq@163.com
  • 基金资助:
    国家自然科学基金(52472018, 52002387)

Effects of High-Entropy Rare-Earth Oxide Addition on the Structure and Long-term High-temperature Stability of BaO-CaO-Al2O3-B2O3-SiO2 Sealing Glass

CHENG Zhenqian1,2, SHI Zhengnan3, ZHANG Biao1, LIU Yang2, SUN Luesheng2, LIN Huixing3, YE Feng1, REN Haishen3   

  1. 1. School of Materials Science and Engineering, Harbin University of Science and Technology, Harbin 150001, China;
    2. The 49th Research Institute of China Electronics Technology Group Corporation, Harbin 150028, China;
    3. Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 201899, China
  • Received:2026-05-08 Revised:2026-07-05
  • About author:CHENG Zhenqian (1985-), male, PhD candidate. E-mail: chengzq@163.com
  • Supported by:
    National Natural Science Foundation of China (52472018, 52002387)

摘要: BaO-CaO-Al2O3-B2O3-SiO2系微晶玻璃因其高膨胀系数与优异的耐高温性能,已成为高温密封领域研究的研究重点,本工作研究添加多种稀土氧化物(Ln2O3,Ln=La、Nd、Sm、Tb、Y、Er、Yb、Sc)后,稀土氧化物熵值变化对BCABS-Ln系列玻璃网络结构、热学行为、结晶性能与高温性能的影响。结果表明,随着稀土元素添加种类从3增加至8,玻璃网络中[BO3]向[BO4]转变,Qn结构单元向高聚合度方向演化,网络连接性显著增强。结合分子动力学模拟,随着熵值增加,桥氧含量由47.9%提高至54.8%,硼氧配位结构重构引起Si-O-B桥联结构的增加。同时,在高熵体系中稀土阳离子呈现局域富集特征。随稀土氧化物熵值增加,玻璃化转变温度(Tg)在684.6~694.7 ℃范围逐渐升高,而析晶峰强度则逐渐降低。在长达10000 h热处理过程中,各组分BCABS-Ln系封接玻璃的主要结晶相均为高稳定Ba0.9Ca0.1SiO3相,热膨胀系数(CTE)变化在9.67×10-6~11.34×10-6 K-1(30~550 ℃)范围,其中稀土元素添加种类为5(La、Nd、Sm、Er、Yb)的组分在长时间保温过程CTE下降率仅2.0%。引入的高熵稀土氧化物通过调控玻璃网络结构与局域配位环境,协同提高了BCABS玻璃的网络聚合度与热稳定性,说明其在固体氧化物燃料电池、氧传感器等高温封接材料中的应用前景。

关键词: 耐高温封接玻璃, 分子动力学模拟, 稀土氧化物, 高熵

Abstract: BaO-CaO-Al2O3-B2O3-SiO2 glass-ceramics have attracted significant attention in high-temperature sealing applications due to their high coefficient of thermal expansion (CTE) and excellent high-temperature resistance. In this work, multiple rare-earth oxides (Ln2O3, Ln = La, Nd, Sm, Tb, Y, Er, Yb, Sc) were introduced, and the effect of configurational entropy on the network structure, thermal behavior, crystallization characteristics, and high-temperature performance of BCABS-Ln glasses were systematically investigated. The results show that as the number of rare-earth components increases from 3 to 8, the glass network evolves toward a higher degree of polymerization, accompanied by the transformation of [BO3] to [BO4] units and enhanced network connectivity. Combined with molecular dynamics simulations, the bridging oxygen content increases from 47.9% to 54.8% with increasing entropy, and the reconstruction of boron coordination leads to an increase in Si-O-B linkages. Meanwhile, rare-earth cations exhibit local enrichment in the high-entropy system. With increasing entropy, the glass transition temperature (Tg) gradually rises within the range of 684.6-694.7 ℃, while the crystallization peaks decrease, indicating suppressed crystallization. During long-term heat treatment up to 10000 h, the dominant crystalline phase of BCABS-Ln glass-ceramics remains the highly stable Ba0.9Ca0.1SiO3 phase. The CTE values range from 9.67 × 10-6 to 11.34 × 10-6 K-1 (30-550 °C), the composition containing five rare-earth elements (La, Nd, Sm, Er, and Yb) exhibits a CTE degradation of only 2.0% after long-term thermal exposure. The introduction of high-entropy rare-earth oxides effectively enhances the network polymerization and thermal stability of BCABS glasses through the synergistic regulation of network structure and local coordination environments, demonstrating promising potential for applications in high-temperature sealing materials such as solid oxide fuel cells and oxygen sensors.

Key words: high-temperature sealing glass, molecular dynamics simulation, rare-earth oxides, high entropy

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