| Literature DB >> 31736151 |
Dharmaraj Periyanagounder1, Tzu-Chiao Wei1, Ting-You Li1,2, Chun-Ho Lin1, Théo Piechota Gonçalves3, Hui-Chun Fu1, Dung-Sheng Tsai1, Jr-Jian Ke1, Hung-Wei Kuo4, Kuo-Wei Huang3, Norman Lu2,4, Xiaosheng Fang5, Jr-Hau He1,6.
Abstract
Organic semiconductors demonstrate several advantages over conventional inorganic materials for novel electronic and optoelectronic applications, including molecularly tunable properties, flexibility, low-cost, and facile device integration. However, before organic semiconductors can be used for the next-generation devices, such as ultrafast photodetectors (PDs), it is necessary to develop new materials that feature both high mobility and ambient stability. Toward this goal, a highly stable PD based on the organic single crystal [PtBr2 (5,5'-bis(CF3 CH2 OCH2 )-2,2'-bpy)] (or "Pt complex (1o)") is demonstrated as the active semiconductor channel-a material that features a lamellar molecular structure and high-quality, intraligand charge transfer. Benefitting from its unique crystal structure, the Pt-complex (1o) device exhibits a field-effect mobility of ≈0.45 cm2 V-1 s-1 without loss of significant performance under ambient conditions even after 40 days without encapsulation, as well as immersion in distilled water for a period of 24 h. Furthermore, the device features a maximum photoresponsivity of 1 × 103 A W-1 , a detectivity of 1.1 × 1012 cm Hz1/2 W-1 , and a record fast response/recovery time of 80/90 µs, which has never been previously achieved in other organic PDs. These findings strongly support and promote the use of the single-crystal Pt complex (1o) in next-generation organic optoelectronic devices.Entities:
Keywords: fluorine functionalization; metal-ligand charge transfer; organic photodetectors; organic semiconductors; transfer integrals
Year: 2019 PMID: 31736151 DOI: 10.1002/adma.201904634
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849