CdSe Quantum Dots Enable High Thermoelectric Performance in Solution‐Processed Polycrystalline SnSe

Author:

Dou Wei1,Gong Yaru1,Huang Xinqi1,Li Yanan1,Zhang Qingtang1,Liu Yuqi1,Xia QinXuan1,Jian Qingyang1,Xiang Deshang1,Li Di2,Zhang Dewei3,Zhang Shihua1,Ying Pan1,Tang Guodong1ORCID

Affiliation:

1. National Key Laboratory of Advanced Casting Technologies, MIIT Key Laboratory of Advanced Metallic and Intermetallic Materials Technology, Engineering Research Center of Materials Behavior and Design Ministry of Education Nanjing University of Science and Technology Nanjing 210094 China

2. Key Laboratory of Materials Physics Institute of Solid State Physics Chinese Academy of Sciences Hefei 230031 China

3. School of Materials Science and Engineering Yancheng Institute of Technology Jiangsu 221051 China

Abstract

AbstractHere, a high peak ZT of ≈2.0 is reported in solution‐processed polycrystalline Ge and Cd codoped SnSe. Microstructural characterization reveals that CdSe quantum dots are successfully introduced by solution process method. Ultraviolet photoelectron spectroscopy evinces that CdSe quantum dots enhance the density of states in the electronic structure of SnSe, which leads to a large Seebeck coefficient. It is found that Ge and Cd codoping simultaneously optimizes carrier concentration and improves electrical conductivity. The enhanced Seebeck coefficient and optimization of carrier concentration lead to marked increase in power factor. CdSe quantum dots combined with strong lattice strain give rise to strong phonon scattering, leading to an ultralow lattice thermal conductivity. Consequently, high thermoelectric performance is realized in solution‐processed polycrystalline SnSe by designing quantum dot structures and introducing lattice strain. This work provides a new route for designing prospective thermoelectric materials by microstructural manipulation in solution chemistry.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

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