RESUMEN
Formamidinium lead bromide (FAPbBr3) nanocrystals have emerged as a powerful platform for optoelectronic applications due to their pure green photoluminescence (PL). However, their low colloidal stability under storage and operation reduces the potential use of FAPbBr3 perovskite nanocrystals (PeNCs) in various applications. In this study, we prepared the poly(L-lactic acid) (PLLA) nanofibrous membrane embedded with FAPbBr3 perovskite nanocrystals by electrospinning the perovskite and PLLA precursor solution. This is a simple and low-cost technique for the direct confinement of nano-sized functional materials in the continuous polymer nanofibres. PLLA as a polymer matrix provided a high surface framework to fully encapsulate the perovskite NCs. In addition, we found that FAPbBr3 PeNCs crystallize spontaneously inside the PLLA nanofibre. The resultant PLLA-FAPbBr3 nanofibrous membranes were stable and remained in the water for about 45 days without any evident decomposition. The results of this research support the idea of new possibilities for the production of air-stable FAPbBr3 PeNCs by forming a composite with PLLA polymer. The authors believe this study is a new milestone in the development of highly stable metal halide perovskite-based nanofibres, which allow for potential use in lasers, waveguides, and flexible energy harvesters.
RESUMEN
Porous poly(L-lactic acid) (PLLA) nanofibrous membrane with the high surface area was developed by electrospinning and post acetone treatment and used as a substrate for deposition of chitosan. Chitosan was coated onto porous nanofibrous membrane via direct immersion coating method. The porous PLLA/chitosan structure provided chitosan a high surface framework to fully and effectively adsorb heavy metal ions from water and showed higher and faster ion adsorption. The composite membrane was used to eliminate copper ions from aqueous solutions. Chitosan acts as an adsorbent due to the presence of aminic and hydroxide groups which are operating sites for the capture of copper ions. The maximum adsorption capacity of copper ions reached 111.66 ± 3.22 mg/g at pH (7), interaction time (10 min) and temperature (25 °C). The adsorption kinetics of copper ions was established and was well agreed with the second-order model and Langmuir isotherm. Finally, the thermodynamic parameters were studied.
