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Immobilization of single antioxidant enzyme systems was frequently studied in the past, however, there is a lack of reliable reports on the co-immobilization of such enzymes. Here, an antioxidant enzyme cascade involving superoxide dismutase (SOD) and horseradish peroxidase (HRP) was successfully immobilized on titania nanosheets (TNS) by the sequential adsorption method using poly(diallyldimethylammonium chloride) (PDADMAC) and poly(styrene sulfonate) (PSS) polyelectrolyte building blocks. The development of the cascade system was based on a colloid approach, in which the charging and aggregation processes were optimized in each synthetic step. The polyelectrolyte and enzyme multilayers were built up in two different sequences at the particle interface, namely, TNS-PDADMAC-SOD-PSS-HRP and TNS-HRP-PDADMAC-SOD-PSS. The formation of the polyelectrolyte layers led to charge reversal of the carrier and the saturated PDADMAC and PSS layers stabilized the dispersions, in particular, their resistance against salt-induced aggregation was especially excellent. The results of enzymatic assays revealed that the SOD and HRP-like activities of the composites depended on the location of the enzymes in the hybrid material. The obtained compounds showed remarkable antioxidant effect and were able to simultaneously decompose superoxide radical anions and hydrogen peroxide. The cascade systems are of great promise in industrial manufacturing processes during the preparation of high-quality products without any damages by reactive oxygen species.Potential strategies such as surface passivation and perovskite material halide mixing may protect material surfaces, improve luminescence, and reduce charge traps for device stability. In this study, we used deep level transient spectroscopy to investigate the effect of CdSe/ZnS core-shell quantum dots (QDs) on defect states and carrier transport in methylammonium (MA) lead halide perovskites (CH3NH3PbX3 where X = I, Br). In MAPbI3 and MAPbI2Br films with CdSe/ZnS QDs, the density of hole traps located at Ev + 0.37 eV and Ev + 0.56 eV was reduced dramatically. Deep traps at Ev + 0.78 eV and Ev + 1.08 eV were removed, and one broad electron trap signal dominated. Film photoresponsivity under 600-nm wavelength light and a bias voltage of -0.7 V was 10 and 18 mA/W, which is 100 and 27 times larger than the 0.1 and 0.67 mA/W of bare perovskites (PS), respectively. This demonstrates that carrier transport was enhanced due to defect suppression. Our findings on defect suppression and photoresponsivity enhancement provide an important direction for optimizing high-performance PS device fabrication.The low mass activity and high price of pure platinum (Pt)-based catalysts predominantly limit their large-scale utilization in electrocatalysis. Therefore, the reduction of Pt amount while preserving the electrocatalytic efficiency represents a viable alternative. In this work, we prepared new PtRu2 nanoparticles supported on sulphur and nitrogen co-doped crumbled graphene with trace amounts of iron (PtRu2/PF) electrocatalysts. The PtRu2/PF catalysts exhibited enhanced electrocatalytic performance and stability for the hydrogen evolution reaction (HER) at pH = 0. Moreover, the prepared PtRu2/PF electrocatalyst displayed higher HER activity than commercial 20% Pt/C. The PtRu2/PF catalyst achieved a current density of 10 mA cm-2 at an overpotential value of only 22 mV for HER, performing better activity than many other Pt-based electrocatalysts. Besides, the PtRu2/PF revealed a good performance for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in alkaline media. The PtRu2/PF catalyst recorded a current density of 10 mA cm-2 at an overpotential of only 270 mV for OER in KOH (1.0 M) solution and an onset potential of 0.96 V vs. RHE (at 1 mA cm-2) for ORR in KOH (0.1 M) solution.Addressing the inherent holes transport limitation of BiVO4 photoanode is crucial to achieve efficient photoelectrochemical (PEC) water splitting. The construction of the hole-transfer bridge between co-catalysts and BiVO4 photoanode could be an effective way to overcome sluggish hole-transfer kinetics of BiVO4 photoanode. Herein, CxNy/BiVO4 photoanode was prepared by coupling carbon nitride hydrogel (CNH) containing unsaturated N on the BiVO4 photoanode during annealing. CxNy/BiVO4 photoanode exhibited excellent PEC performance and stability. Photoelectrochemical tests proved that the coupling of CxNy accelerated holes transfer and enhanced oxygen evolution kinetics. learn more X-ray photoelectron spectroscopy (XPS) and theoretical calculations confirmed the existence of the BiNV bond between BiVO4 photoanode and CxNy, which could serve as the hole-transfer bridge to significantly accelerate separation and transfer of carriers driven by the interfacial electric field. Moreover, it was found that the coupling of CxNy effectively inhibited the dissociation of metal ions through changing their coordination environment, resulting in the excellent stability of CxNy/BiVO4 photoanode. This result provides unique insights into vital roles of the interfacial structure, which might have a significant impact on the construction of PEC devices.Color changeable photonic prints (CCPPs) show their potential applications in high-level information storage and anti-counterfeiting, but usually suffer from the complex fabrication process and limited color variation. Here, a simple and efficient method is developed to generate CCPPs with multilevel tunable color contrasts by packing the solvent responsive photonic crystals with diverse cross-linking degrees and desired way. The key to the successful fabrication is to create and control over the optical response of each part of the CCPPs through altering the cross-linking degree of PCs and thus the affinity between the CCPPs and solvents. A CCPPs based anti-fake label with the encrypted information functionality which originates from reversible color change between dried state and swelling with the mixture of acetic acid and ethanol is investigated. Compared with conventional CCPPs, the as-prepared CCPPs can reveal multistage information depending on the volume fraction of ethanol. This work provides a new insight for the simple fabrication of CCPPs and will facilitate their applications in the information protection and high-level anti-counterfeiting.