2 research outputs found
Doping Zn<sup>2+</sup> in CuS Nanoflowers into Chemically Homogeneous Zn<sub>0.49</sub>Cu<sub>0.50</sub>S<sub>1.01</sub> Superlattice Crystal Structure as High-Efficiency <i>n</i>‑Type Photoelectric Semiconductors
Doping
Zn<sup>2+</sup> in CuS nanoflower into chemically homogeneous superlattice
crystal structure is proposed to convert <i>p</i>-type CuS
semiconductor to an <i>n</i>-type CuS semiconductor for
significantly enhanced photoelectric response performance. In this
study, the chemically homogeneous Zn-doped CuS nanoflowers (Zn<sub>0.06</sub>Cu<sub>0.94</sub>S, Zn<sub>0.26</sub>Cu<sub>0.73</sub>S<sub>1.01</sub>, Zn<sub>0.36</sub>Cu<sub>0.62</sub>S<sub>1.02</sub>, Zn<sub>0.49</sub>Cu<sub>0.50</sub>S<sub>1.01</sub>, Zn<sub>0.58</sub>Cu<sub>0.40</sub>S<sub>1.02</sub>) are synthesized by reacting appropriate
amounts of CuCl and ZnÂ(Ac)<sub>2</sub>·2H<sub>2</sub>O with sulfur
powders in ethanol solvothermal process. By tuning the Zn/Cu atomic
ratios to ∼1:1, the chemically homogeneous Zn-doped CuS nanoflowers
could be converted to the perfect Zn<sub>0.49</sub>Cu<sub>0.50</sub>S<sub>1.01</sub> superlattice structure, corresponding to the periodic
Cu–S–Zn atom arrangements in the entire crystal lattice,
which can induce an effective built-in electric field with <i>n</i>-type semiconductor characteristics to significantly improve
the photoelectric response performance, such as the lifetime of photogenerated
charge carriers up to 6 × 10<sup>–8</sup>–6 ×
10<sup>–4</sup> s with the transient photovoltage (TPV) response
intensity to ∼44 mV. This study reveals that the Zn<sup>2+</sup> doping in CuS nanoflowers is a key factor in determining the superlattice
structure, semiconductor type, and the dynamic behaviors of charge
carriers
Multicolor Fluorescent Inks Based on Lanthanide Hybrid Organogels for Anticounterfeiting and Logic Circuit Design
With the rapid development of information technology,
the encrypted
storage of information is becoming increasingly important for human
life. The luminescent materials with a color-changed response under
physical or chemical stimuli are crucial for information coding and
anticounterfeiting. However, traditional fluorescent materials usually
face problems such as a lack of tunable fluorescence, insufficient
surface-adaptive adhesion, and strict synthesis conditions, hindering
their practical applications. Herein, a series of luminescent lanthanide
hybrid organogels (Ln-MOGs) were rapidly synthesized using a simple
method at room temperature through the coordination between lanthanide
ions and 2,6-pyridinedicarboxylic acid and 5-aminoisophthalic acid.
And the multicolor fluorescent inks were also prepared based on the
Ln-MOG and hyaluronic acid, with the advantages of being easy to write,
color-adjustable, and water-responsive discoloration, which has been
applied to paper-based anticounterfeiting technology. Inspired by
the responsiveness of the fluorescent inks to water, we designed a
logic system that can realize single-input logic operations (NOT and
PASS1) and double-input logic operations (NAND, AND, OR, NOR, XOR).
The encryption of a binary code can be actualized utilizing different
luminescent response modes based on the logic circuit system. By adjusting
the energy sensitization and luminescence mechanism of lanthanide
ions in the gel structure, the information reading and writing ability
of the fluorescent inks were verified, which has great potential in
the field of multicolor pattern anticounterfeiting and information
encryption