Advancing Ag<sub>2</sub>Se thin-film thermoelectrics via selenization-driven anisotropy control.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39934123.
- Also identified by DOI 10.1038/s41467-025-56671-7 and PMC identifier 11814352.
- Licence recorded as CC BY-NC-ND.
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Abstract
The debate over the optimal orientation of Ag<sub>2</sub>Se thin films and its influence on thermoelectric performance remains ongoing. Here, we report a wet-chemical selenization-based anisotropy optimization technique to control the in-plane orientation of the Ag<sub>2</sub>Se thin film, steering it away from (002) nearly parallel planes that hinder charge carrier mobility. This approach enables us to achieve an impressive power factor of 30.8 μW cm<sup>-1</sup> K<sup>-2</sup> at 343 K. The as-fabricated Ag<sub>2</sub>Se thin film demonstrates remarkable durability, retaining over 90% of its power factor after six months of air exposure, and outstanding flexibility, with performance variation staying within 5% after 2000 bending cycles at a 5 mm radius. These attributes are attributed to the controlled film thickness, crystallinity, and strong adhesion to the polyimide substrate. Additionally, the as-assembled slotted thermoelectric device delivers an output power of 0.58 μW and a competitive power density of 807 μW cm<sup>-2</sup> at a temperature difference of 20 K, alongside a high normalized power density of 1.8 μW cm<sup>-2</sup> K<sup>-2</sup>, highlighting its potential for practical application. This study provides valuable insights into the design of high-performance, highly flexible thermoelectric thin films for real-world applications.