RESUMEN
Polyimide (PI) is one of the most dominant engineering plastics with excellent thermal, mechanical, chemical stability and dielectric performance. Further improving the versatility of PIs is of great significance, broadening their application prospects. Thus, integrating functional nanofillers can finely tune the individual characteristic to a certain extent as required by the function. Integrating the two complementary benefits, PI-based composites strongly expand applications, such as aerospace, microelectronic devices, separation membranes, catalysis, and sensors. Here, from the perspective of system science, the recent studies of PI-based composites for molecular design, manufacturing process, combination methods, and the relevant applications are reviewed, more relevantly on the mechanism underlying the phenomena. Additionally, a systematic summary of the current challenges and further directions for PI nanocomposites is presented. Hence, the review will pave the way for future studies.
RESUMEN
CsPbI3 perovskite nanocrystals (NCs) have recently emerged as promising materials for optoelectronic devices because of their superior properties. However, the poor stability of the CsPbI3 NCs induced by easy ligand desorption represents a key issue limiting their practical applications. Herein, we report stable and highly luminescent black-phase CsPbI3 NCs passivated by novel ligands of sodium dodecyl sulfate (SDS). Theoretical calculation results reveal a stronger adsorption energy of SDS molecules at the CsPbI3 surface than that of commonly used oleic acid. As a result, the defect formation caused by the ligand loss during the purification process is greatly suppressed. The optimized SDS-CsPbI3 NCs exhibit significantly reduced surface defects, much enhanced stability, and superior photoluminescence efficiency. The red perovskite light-emitting diodes based on the SDS-CsPbI3 NCs demonstrate an external quantum efficiency of 8.4%, which shows a 4-fold improvement compared to the devices based on the oleic acid-modified CsPbI3 NCs.
RESUMEN
Flexible surface-enhanced Raman scattering (SERS) sensors have attracted great attention as a portable and low-cost device for chemical and bio-detection. However, flexible SERS sensors tend to suffer low signal spatial homogeneity due to the uneven distribution of active plasmonic nanostructures (hot spots) and quick degradation of their sensitivity due to low adhesion of hot spots and flexible substrates during fast sampling. Herein, a large-area (20 × 20 cm2) polyimide (PI)-based SERS sensor is exploited for trace detection with high signal homogeneity and stability. The SERS sensor is constructed from PI through in situ growth of silver and gold core-shell nanoparticles (Ag@Au NPs) based on chemical reduction and galvanic replacement processes. Benefiting from the abundant carboxyl groups on the surface-cleaved PI, densely and uniformly distributed Ag@Au NPs are successfully prepared on the film under ambient conditions. The high Raman enhancement factor (EF) (up to 1.07 × 107) and detection capability with low nanomolar (10-9 M) detection limits are obtained for this flexible SERS sensor. The uniform Raman signals in the random region show good signal homogeneity with a low variation of 8.7%. Moreover, the flexible SERS sensor exhibited superior efficiency and durability after storage for 30 days even after 500 cycles of mechanical stimuli (bending or torsion). The residue of pesticide thiram (tetramethylthiuram disulfide, TMTD) has been rapidly traced by direct sampling from the apple surface, and a sensitivity of 10 ng/cm2 for TMTD was achieved. These findings show that the PI-based SERS sensor is a very strong candidate for broad and simple utilization of flexible SERS for both laboratory and commercial applications in chemical and biomolecule detections.
RESUMEN
An eco-friendly n-type water/alcohol-soluble conjugated polyelectrolyte PFEO SO3 Li was synthesized and applied as a cathode interfacial layer in organic solar cells. The π-delocalized polyfluorene backbone has an intimate connection with the hydrophobic active layer, and the side chain with lithium ion may move toward the ZnO layer through the self-assembly property of conjugated polyelectrolytes. UV photoelectron spectroscopy indicated that modification with PFEO SO3 Li dramatically lowers the work function of indium-doped tin oxide (ITO)/ZnO and may form strong interfacial dipoles between ZnO and the active layer. Meanwhile, introduction of lithium ions as spectator cations may contribute to reduction of the intrinsic surface defects of ZnO. The green emission in the photoluminescence spectrum of ZnO disappeared after modification with PFEO SO3 Li. In addition, the roughness of ZnO barely changed after coating with PFEO SO3 Li, and the surface became more hydrophobic, which demonstrates that the thin conjugated polyelectrolyte layer exhibits good adhesion with both ZnO and the active layer. These phenomena indicate that the introduction of PFEO SO3 Li makes ITO/ZnO an efficient cathode. As a result, inverted organic solar cell devices with ZnO/PFEO SO3 Li double-interlayers exhibit high efficiencies of 11.7 and 10.6 % for PBDB-T:IT-M and PBDB-T:ITIC blend systems, respectively.
RESUMEN
We report about a flexible substrate incorporating surface-confined silver nanoparticles on transparent polyimide (PI). The incorporated silver nanoparticles (Ag NPs), which possessed excellent adhesive strength with the PI substrate, induced localized surface plasmon resonance and light scattering effects by changing the particle size and interparticle distance to promote light harvesting in the perovskite solar cells. Moreover, the reduced sheet resistance was beneficial for the charge extraction and transportation in the devices when high-conductivity poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS, PH1000) was deposited on the Ag NP-confined PI serving as a flexible bottom electrode. A power conversion efficiency of 10.41% was obtained for the flexible perovskite solar cells based on a Ag NP-confined PI substrate (the particle size of the Ag NPs was 25 nm mixed with 40 nm), which was obviously enhanced in all parameters. Especially, a 61% improvement existed in the short-circuit current density compared to that based on the bare PI substrates. It indicates that the substrate would be a promising candidate for the development of flexible electronics.