4.8 Article

Enhanced Stability and Thermoelectric Performance in Cu1.85Se-Based Compounds

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 31, Pages 37862-37872

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c08886

Keywords

thermoelectric; Cu1.85Se; cubic; stability; ZT

Funding

  1. National Key and Development Program of China [2017YFC0602102]
  2. National Natural Science Foundation of China [U20A20213, 61727818]
  3. Department of Science and Technology of Sichuan Province [2021JDTD0030]
  4. Chengdu Science and Technology Project [2020-GH02-0065HZ]

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Recent studies have found that co-doping with Li/Bi can effectively optimize the hole concentration in cubic copper selenium-based compounds, significantly improving their thermoelectric performance and exhibiting outstanding critical voltage values at high temperatures. Additionally, alloying sulfur in these compounds can greatly reduce thermal conductivity, further enhancing thermoelectric performance.
Liquid-like copper selenium compounds have attracted considerable interest in recent years for their excellent thermoelectric performance, abundant element reserves, and low toxicity. However, the related applications are still limited due to the phase transition and precipitation of Cu under an external field. Here, the cubic Cu1.85Se-based compounds with suppressed phase transition and improved critical voltage (V-c) are first studied. In particular, Li/Bi co-doping effectively optimizes hole concentration and the ZTs are substantially improved from 0.2 in Cu1.85Se to 0.7 in Li0.03Cu1.81Bi0.04Se at 760 K. Meanwhile, the latter shows an outstanding V-c above 0.22 V at 750 K, which is the highest value in Cu2-xSe thermoelectric compounds to date. Moreover, S is alloyed in Li0.03Cu1.81Bi0.04Se to greatly reduce the thermal conductivity and the ZT is further enhanced to 0.9 for Li0.03Cu1.81Bi0.04Se0.9S0.1 at 760 K. Our work sheds light on a new strategy to realize good stability and enhanced thermoelectric performance, which provides a new direction for further research.

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