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Synthesis and electronic structure of van der Waals layered Cu1.1Fe1.2Te2 with a spin-density-wave behavior.

Authors :
Feng, Yan
Yang, Haifeng
Wei, Zhiyuan
Wang, Zhi
Zhang, Ying
Wang, Shasha
Ma, Xiang
Ou, Zhipeng
Lu, Yalin
He, Junfeng
Liu, Zhongkai
Xiang, Bin
Source :
Journal of Materials Science; Jun2023, Vol. 58 Issue 23, p9579-9585, 7p, 3 Graphs
Publication Year :
2023

Abstract

Recent research has demonstrated that the CuFeTe<subscript>2</subscript> compound has interesting physical properties. However, less research effort has been afforded to the study of the stable non-stoichiometric Cu<subscript>1.1</subscript>Fe<subscript>1.2</subscript>Te<subscript>2</subscript> structure and electronic properties. In this paper, we report the synthesis and electronic properties of the non-stoichiometric (Cu, Fe) co-doped CuFeTe<subscript>2</subscript> (Cu<subscript>1.1</subscript>Fe<subscript>1.2</subscript>Te<subscript>2</subscript>) with a stable single phase. The temperature-dependent resistance and magnetic susceptibility measurements showed an obvious phase transition from a semiconductor to metal when the temperature reached 360 K, revealing a spin-density-wave (SDW)-like state existing in the as-grown Cu<subscript>1.1</subscript>Fe<subscript>1.2</subscript>Te<subscript>2</subscript>, which has a higher SDW transition temperature than that of CuFeTe<subscript>2</subscript>. Interestingly, a spectral weight evolution of the angle-resolved photoemission spectroscopy in the study of the electronic structure of Cu<subscript>1.1</subscript>Fe<subscript>1.2</subscript>Te<subscript>2</subscript> is observed at the same temperature of 360 K. Our work provides a scheme for exploration of novel physical phenomena related to SDW in two-dimensional materials. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222461
Volume :
58
Issue :
23
Database :
Complementary Index
Journal :
Journal of Materials Science
Publication Type :
Academic Journal
Accession number :
164263502
Full Text :
https://doi.org/10.1007/s10853-023-08626-w