Negative Thermal Expansion in the Noncarboxylate Based Metal-Organic Framework Cd(trz)Cl

被引:4
作者
Liu, Zhanning [1 ,2 ]
Fan, Longlong [3 ]
Xing, Chengyong [1 ]
Wang, Zhe [4 ]
机构
[1] Shandong Univ Sci & Technol, Sch Mat Sci & Engn, Qingdao 266590, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[4] China Univ Petr East China, Sch Mat Sci & Engn, Qingdao 266580, Shandong, Peoples R China
来源
ACS MATERIALS LETTERS | 2023年 / 5卷 / 07期
基金
中国国家自然科学基金;
关键词
FLEXIBILITY; STABILITY;
D O I
10.1021/acsmaterialslett.3c00425
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Negative thermal expansion (NTE), as a counterintuitivephenomenon,has attracted considerable interest owing to its great scientificand technical value. Owing to the inherent structural flexibility,metal-organic frameworks (MOFs) have recently been recognizedas an ideal platform for the study of NTE. However, the reported NTEMOFs are mainly restrained in the carboxylate based ones. Herein,we found that the noncarboxylate MOF Cd(trz)Cl (trz = 1,2,4-trizaole) can also exhibit intrinsic volumetric NTE, anda transition from NTE to PTE at high temperatures can be observed.The combined in situ synchrotron powder X-ray diffraction,Raman spectra measurements, and DFT calculations shed light on thefact that the NTE mainly originates from the synergistic effect ofgeometric flexibility and the enhanced out-of-plane rotation behaviorof the trz ligand. This study not only demonstratesa new NTE material but also can help to extend the scope of NTE tothe more diverse noncarboxylate based MOFs.
引用
收藏
页码:1911 / 1915
页数:5
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