Herein, we report a flexible high-conductivity transparent electrode (denoted as S-PH1000), based on conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), and itsapplication to flexible semi-transparentsupercapacitors. A high conductivity of 2673 S/cm was achieved for the S-PH1000 electrode on flexible plastic substrates via a H₂SO₄ treatment with an optimized concentration of 80 wt.%. This is among the top electrical conductivities of PEDOT:PSS films processed on flexible substrates. As for the electrochemical properties,a high specific capacitance of 161F/g was obtained from the S-PH1000 electrode at a current density of 1 A/g. Excitingly, a specific capacitance of 121 F/g was retained even when the current density increased to 100 A/g, which demonstrates the high-rate property of this electrode. Flexible semi-transparent supercapacitors based on these electrodes demonstrate high transparency, over 60%, at 550 nm. A high power density value, over 19,200 W/kg,and energy density, over 3.40 Wh/kg, was achieved. The semi-transparent flexible supercapacitor was successfully applied topower a light-emitting diode.

Diagnostic approaches based on multimodal imaging of clinical noninvasive imaging (eg. MRI/CT scanner) are highly developed in recent years for accurate selection of the therapeutic regimens in critical diseases. Therefore, it is highly demanded in the development of appropriate all-in-one multimodal contrast agents (MCAs) for the MRI/CT multimodal imaging. Here a novel ideal MCAs (F-AuNC@Fe₃O₄) were engineered by assemble Au nanocages (Au NC) and ultra-small iron oxide nanoparticles (Fe₃O₄) for simultaneous T₁–T₂dual MRI and CT contrast imaging. In this system, the Au nanocages offer facile thiol modification and strong X-ray attenuation property for CT imaging. The ultra-small Fe₃O₄ nanoparticles, as excellent contrast agent, is able to provide great enhanced signal of T₁- and T₂-weighted MRI (r₁ = 6.263 mM⁻¹ s⁻¹, r₂ = 28.117 mM⁻¹ s⁻¹) due to their ultra-refined size. After functionalization, the present MCAs nanoparticles exhibited small average size, low aggregation and excellent biocompatible. In vitro and In vivo studies revealed that the MCAs show long-term circulation time, renal clearance properties and outstanding capability of selective accumulation in tumor tissues for simultaneous CT imaging and T₁- and T₂-weighted MRI. Taken together, these results show that as-prepared MCAs are excellent candidates as MRI/CT multimodal imaging contrast agents.

Aggregation-induced emission has provided fluorescence enhancement strategies for metal nanoclusters. However, the morphology of the aggregated nanoclusters tended to be irregular due to the random aggregated route, which would result in the formation of an unstable product. Herein, copper nanoclusters were directly synthesized by using l-cysteine as both the reducing and protection ligand. Initially, the structure of the product was irregular. Furthermore, Ce³⁺ was introduced to re-arrange the aggregates through a crosslinking avenue. It was interesting to find that well-ordered three-dimensional nanomaterials with mesoporous sphere structures were obtained after re-aggregation. On the basis of the stability test at a relatively high temperature and the light-emitting diode fabrication investigation, it revealed that the regulated product demonstrated more promising stability and color purity for practical applications than the random aggregated product with irregular structures.