Semiconducting High-Entropy Chalcogenide Alloys with Ambi-ionic Entropy Stabilization and Ambipolar Doping

被引:47
作者
Deng, Zihao [1 ]
Olvera, Alan [1 ]
Casamento, Joseph [1 ]
Lopez, Juan S. [1 ]
Williams, Logan [1 ]
Lu, Ruiming [1 ]
Shi, Guangsha [1 ]
Poudeu, Pierre F. P. [1 ]
Kioupakis, Emmanouil [1 ]
机构
[1] Univ Michigan, Mat Sci & Engn, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
HIGH THERMOELECTRIC PERFORMANCE; TEMPERATURE; GETE;
D O I
10.1021/acs.chemmater.0c01555
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Entropy stabilization is a novel materials-design paradigm to realize new compounds with widely tunable properties. However, almost all entropystabilized materials so far are either conducting metals or insulating ceramics, with a clear dearth in the semiconducting regime. Here, a new class of the multicationic and -anionic entropy-stabilized chalcogenide alloys based on the (Ge,Sn,Pb)(S,Se,Te) formula are synthesized and characterized experimentally. The configurational entropy from the disorder of both the anion and the cation sublattices reaches a record value of similar to 2.2 R mol(-1) for the equimolar composition and stabilizes the singlephase solid solution. Theoretical calculations and experiments both show that the synthesized alloys are thermodynamically stable at the growth temperature and kinetically metastable at room temperature, segregating by spinodal decomposition at moderate temperatures. Doping and electronic transport measurements verify that the synthesized materials are ambipolarly dopable semiconductors, which pave the way for the wider adoption of entropy-stabilized chalcogenide alloys in functional applications.
引用
收藏
页码:6070 / 6077
页数:8
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