RESUMEN
Single imidazolate framework-67 (ZIF-67) is commonly used as a template to prepare layered double hydroxides (LDHs) with specific morphology to improve the performance of materials. Herein, the Co2+ ion in ZIF-67 is partially substituted by Ni2+ to obtain the dodecahedron bimetallic imidazolate framework (CoNi-ZIF). Subsequently, using bimetallic CoNi-ZIF as the sacrificial template, CoNi-LDH hierarchical hollow cage structures with wrinkled nanosheet arrays are synthesized at room temperature and in aqueous solution by an inexpensive and environment friendly surfactant-free approach. The optimized etched CoNi-LDH4 has a maximum specific capacitance of 1877 F g-1 at a current density of 1 A g-1, and cycling stability of 99.89% after 5000 cycles, which is significantly better than that of ZIF-67 derived CoNi-LDH67 (1357 F g-1 at 1 A g-1, cycling stability of 73.35%). The asymmetric supercapacitor with CoNi-LDH4 as a cathode and activated carbon (AC) as anode has an energy density of 49.3 Wh kg-1 at 750 W kg-1 power output and stable cycling performance (capacity retention of 92.13% after 5000 cycles). This study shows the prospect of bimetallic CoNi-ZIF derived LDHs nanostructures prepared at room temperature and in aqueous solution to improve the performance and stability of supercapacitors.
RESUMEN
In this study, we introduce a biological method for the production of ternary Quantum Dots (QDs): complex nanostructures with tunable optical and structural properties that utilizes post-synthesis modifications through cation exchange. This versatile in-situ cation exchange method being reported for the first time shows great potential for extending the scope of microbial synthesis. By using this bacterial-based method, we easily synthesize and purify CdS, CdSAg, and Ag2S nanocrystals of a size below 15 nm and with variable morphologies that exhibit fluorescence emissions covering a broad spectral range (from 400 to 800 nm). Energy-dispersive X-ray spectroscopy (EDS) results indicate the partial replacement of Cd2+ by Ag+ when AgNO3 concentration is increased. This replacement produces CdSAg ternary QDs hetero-structures with high stability, fluorescence in the NIR-I (700 - 800 nm), and 36.13% quantum yield. Furthermore, this reaction can be extended for the production of soluble Ag2S nanoparticles (NPs) without any traces of Cd. QDs biosynthesized through this cation exchange process display very low toxicity when tested in bacterial or human cell lines. Biosynthesized ternary hetero-structures were used as red fluorescent dyes to label HeLa cells in confocal microscopy studies, which validates its use in bioimaging applications in the near infrared region. In addition, the application of biologically-produced cadmium NPs in solar cells is reported for the first time. The three biosynthesized QDs were successfully used as photosensitizers, where the CdSAg QDs show the best photovoltaic parameters. Altogether, obtained results validate the use of bacterial cells for the controlled production of nanomaterials with properties that allow their application in diverse technologies. We developed a simple biological process for obtaining tunable Quantum Dots (QDs) with different metal compositions through a cation exchange process. Nanoparticles (NPs) are produced in the extracellular space of bacterial cells exposed to cysteine and CdCl2 in a reaction that depends on S2- generation mediated by cysteine desulfhydrase enzymes and uses cellular biomolecules to stabilize the nanoparticle. Using this extracellular approach, water-soluble fluorescent CdS, CdSAg, and Ag2S Quantum Dots with a tunable emission ranging from 400 to 800 nm were generated. This is the first study reporting the use of microorganisms to produce tunable ternary QDs and the first time that a cation exchange process mediated by cells is described. Obtained results validate the use of biological synthesis to produce NPs with new characteristics and opens a completely new research field related to the use of microorganisms to synthesize complex NPs that are difficult to obtain with regular chemical methods.