| Literature DB >> 32003138 |
Xuebing He1, Chuanfeng Wang1, Xi Huang1, Long Jin1, Xiang Chu1, Meilin Xie1, Yiwen Nie1, Yali Xu1, Zhou Peng1, Chaoliang Zhang2, Jun Lu1, Weiqing Yang1.
Abstract
Herein, an all-solid-state sequential self-organization and self-assembly process is reported for the in situ construction of a color tunable luminous inorganic/polymer hybrid with high direct piezoresponse. The primary inorganic self-organization in solid polymer and the subsequent polymer self-assembly are achieved at high pressure with the first utilization of piezo-copolymer (PVDF-TrFE) as the host matrix of guest carbon quantum dots (CQDs). This process induces the spontaneous formation of a highly ordered, microscale, polygonal, and hierarchically structured CQDs/PVDF-TrFE hybrid with multicolor photoluminescence, consisting of very thermodynamic stable polar crystalline nanowire arrays. The electrical polarization-free CQDs/PVDF-TrFE hybrids can efficiently harvest the environmental available kinetic mechanical energy with a new large-scale group-cooperation mechanism. The open-circuit voltage and short-circuit current outputs reach up to 29.6 V cm-2 and 550 nA cm-2 , respectively. The CQDs/PVDF-TrFE-based hybrid nanogenerator demonstrates drastically improved durable and reliable features during the real-time demonstration of powering commercial light emitting diodes. No attenuation/fluctuation of the electrical signals is observed for ≈10 000 continuous working cycles. This study may offer a new design concept for progressively but spontaneously constructing novel multiple self-adaptive complex inorganic/polymer hybrids that promise applications in the next generation of self-powered autonomous optoelectronic devices.Entities:
Keywords: electro-optical materials; photoluminescence; quantum dots; self-organization; self-powered nanosystems
Year: 2020 PMID: 32003138 DOI: 10.1002/smll.201905703
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281