Synthesis of Ti2(InxAl1-x)C (x=0-1) solid solutions with high-purity and their properties

被引:9
|
作者
Tian, Zhihua [1 ]
Yan, Bingzhen [1 ]
Wu, Fushuo [1 ]
Tang, Jingwen [1 ]
Xu, Xueqin [1 ]
Liu, Jian [1 ,2 ]
Zhang, Peigen [1 ]
Sun, ZhengMing [1 ]
机构
[1] Southeast Univ, Sch Mat Sci & Engn, Nanjing 211189, Peoples R China
[2] Wuxi Lintex Adv Mat Co Ltd, Wuxi 214145, Peoples R China
基金
中国国家自然科学基金;
关键词
MAX phases; Ti2(InxAl1-x)C solid solution; Formation mechanism; Mechanical properties; Electrochemical corrosion; MAX PHASE; MECHANICAL-PROPERTIES; CORROSION-RESISTANCE; MICROSTRUCTURE; STABILITY;
D O I
10.1016/j.jeurceramsoc.2023.06.060
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Herein, high-purity Ti2(InxAl1-x)C (x = 0-1) solid solutions were successfully synthesized. The crystal structure and actual composition of solid solutions were confirmed using XRD, SEM, and TEM analyses, and their formation mechanism was revealed by thermal analysis. On the In-rich side (x & GE; 0.5), primary Ti2InC first formed and then acted as a crystalline seed for the subsequent solid solutions, resulting in a cluster-like morphology. The lattice constants of Ti2(InxAl1-x)C were found to well follow Vegard's law. The examined properties of Ti2(InxAl1x)C also greatly depended on their A-site compositions. Ti2AlC exhibited the highest hardness and elastic moduli, while the best corrosion resistance was achieved at Ti2InC, and all Ti2(InxAl1-x)C displayed active dissolution in 0.5 M HCl solution. Thus, adjusting the In/Al ratio at A-site can yield a desired set of performances, which provides a good example for regulating the performance of MAX phases via A-site solid solution strategy.
引用
收藏
页码:5915 / 5924
页数:10
相关论文
共 50 条
  • [21] Synthesis and properties of TlIn1-x Gd x Se2 solid solutions
    Guseinov, Ya Yu
    Bairamov, D. D.
    Mustafaeva, U. M.
    Magerramov, A. B.
    INORGANIC MATERIALS, 2012, 48 (04) : 329 - 331
  • [22] Synthesis and Photoluminescence Properties of Divalent Europium Doped-CaAlSi1+2xN3+2xOx (x=0-1) Solid Solution Phosphors
    Wang, Yao
    Zhao, Fengyang
    Piao, Xianqing
    Sun, Zhuo
    Horikawa, Takashi
    Machida, Ken-ichi
    ECS JOURNAL OF SOLID STATE SCIENCE AND TECHNOLOGY, 2013, 2 (07) : R131 - R134
  • [23] Synthesis and characterization of Co doped Ti1-xCoxO2 {0 < x < 0.30} solid solutions
    Ahmed, Naiem
    Singh, Anupinder
    Sharma, Neha
    Paul, Surinder
    Paul, Surinder
    MATERIALS TODAY-PROCEEDINGS, 2022, 65 : 3288 - 3292
  • [24] High-Purity FeSe1-x Superconductors Prepared by Solid-State Synthesis and Liquid Phase Processing
    Qi, Xiaoding
    Wang, Jiun-Yi
    Hung, Chi-Jung
    Kuo, Jui-Chao
    Yates, Karen
    Cohen, Lesley
    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2010, 93 (10) : 3195 - 3200
  • [25] Synthesis of high-purity Ti2A1N ceramic by hot pressing
    Yan Ming
    Chen Yan-lin
    Mei Bing-chu
    Zhu Jiao-qun
    TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA, 2008, 18 (01) : 82 - 85
  • [26] Semiconducting CuClxBr1-x (x=0-1) nanocrystals in thin films:: synthesis and characterization
    Suyal, G
    Mennig, M
    Schmidt, H
    JOURNAL OF MATERIALS CHEMISTRY, 2002, 12 (10) : 3136 - 3140
  • [27] Vibrational and structural properties of CU2ZnSn(SxSe1-x)4 (0 ≤ x ≤ 1) solid solutions
    Dimitrievska, Mirjana
    Xie, Haibing
    Gurieva, Galina
    Fontane, Xavier
    Fairbrother, Andrew
    Glinder, Rene
    Saucedo, Edgardo
    Perez-Rodriguez, Alejandro
    Schorr, Susan
    Izquierdo-Roca, Victor
    2014 IEEE 40TH PHOTOVOLTAIC SPECIALIST CONFERENCE (PVSC), 2014, : 33 - 36
  • [28] Study On Structural And Optical Properties Of α-(AlxCr1-x)2O3 (0 ≤ x ≤ 1) Solid Solutions
    Jangir, Ravindra
    Kumar, Dharmendra
    Srihari, Velaga
    Ganguli, Tapas
    62ND DAE SOLID STATE PHYSICS SYMPOSIUM, 2018, 1942
  • [30] Phase transition in Eu2Zr2-xO7-2x (x=0-1) solid solutions: A combined structural and spectroscopic study
    Kong, Linggen
    Wang, Zhiyang
    Karatchevtseva, Inna
    Zhang, Yingjie
    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2024, 107 (11) : 7604 - 7618