Isovalent Bi substitution induced low thermal conductivity and high thermoelectric performance in n-type InSb

被引:6
|
作者
Palraj, Jothilal [1 ]
Moorthy, Manojkumar [1 ]
Katlakunta, Sadhana [2 ]
Perumal, Suresh [1 ]
机构
[1] SRM Inst Sci & Technol, Dept Phys & Nanotechnol, Lab Energy & Adv Devices LEAD, Kattankulathur 603203, Tamilnadu, India
[2] Osmania Univ, Univ Coll Sci, Dept Phys, Saifabad, Hyderabad 500004, Telangana, India
关键词
Thermoelectrics; n-type InSb; Thermal conductivity; High zT; Vickers micro-hardness; MECHANICAL-PROPERTIES; MICROSTRUCTURE; PBTE; CONVERGENCE; TRANSPORT; ALLOYS; FIGURE; INAS;
D O I
10.1016/j.ceramint.2022.05.282
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
In this paper, thermoelectric (TE) properties of n-type InSb1-xBix (x = 0.00, 0.02, 0.05 and 0.10) polycrystalline samples, synthesized by single-step vacuum melting reaction, have been studied in the temperature range of 300-623 K. P-XRD confirms the phase purity and preferred orientation of (220) plane. FE-SEM back-scattered electron (BSE) micrographs reveal surface morphology and phase homogeneity, and elemental mapping with EDS is used to identify the chemical composition. The elemental existence and oxidation state of In3+, Sb3+, and Bi3+ in InSb1-xBix are rechecked through XPS analysis. With Bi substitution, the electrical conductivity of InSb increases, whereas Seebeck coefficient starts decreasing. However, the maximum Seebeck coefficient, S of -241 mu V/K at 423 K, was achieved for the composition of InSb0.98Bi0.02. Interestingly, a huge reduction in lattice thermal conductivity, kappa(lattice) from similar to 17.5 W/mK (InSb) to 13.1 W/mK (InSb0.9Bi0.10) at 300 K is observed due to increased phonon scattering from mass-fluctuation and created point defects. Further, the maximum thermoelectric figure of merit, zT was achieved as similar to 0.56 at 623 K with higher Vickers micro-hardness values of similar to 140 HV for the composition of InSb0.98Bi0.02 which is notably higher than the recently reported InSb based materials.
引用
收藏
页码:29284 / 29290
页数:7
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