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Ferrocene Chalcone Enhanced Cyclotriphosphazene Photodiode Systems via Click Chemistry: Their Synthesis, Electrical, and Photophysical Properties. | LitMetric

AI Article Synopsis

  • A new ferrocene-decorated cyclotriphosphazene compound was synthesized using the click method, confirming structures through various spectroscopic techniques.
  • The optical band gaps of the compounds were measured, showing values ranging from 3.46 eV to 4.75 eV, with the final product exhibiting favorable electronic properties based on the hopping conduction mechanism.
  • Diodes made from these compounds demonstrated excellent rectification behavior and photodiode properties under sunlight, suggesting potential applications in optoelectronic devices.

Article Abstract

In this study, a new ferrocene-decorated cyclotriphosphazene compound () was obtained by the interaction of ferrocene chalcone with azide end groups () and spirophosphazene () bearing alkyne groups using the click method. The structures of all compounds were confirmed using Fourier transform infrared, H, C APT, and P NMR, and MS techniques. The optical band gaps of compounds were measured, showing values of 4.75 eV for , 3.53 eV for , and 3.46 eV for final product . The optical band gap of compound calculated by density functional theory is 3.28 eV. The electrical properties of the compounds were investigated against the frequency. The results showed that the conduction mechanism is based on the hopping model. New types of diodes were prepared by using compounds and . The current-voltage characteristics of the compound diode showed good rectification behavior. The rectification ratio of the heterojunction diode was calculated as 629. The ideality factors were 3.35 for and 7.57 for . The barrier heights were 0.68 and 0.92, respectively. Under sunlight (20-100 mW/cm), both diodes exhibited photodiode properties, with compound being more sensitive to light. This indicates that the diodes can be used in optoelectronic devices due to their photoconductive behavior.

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Source
http://dx.doi.org/10.1021/acs.inorgchem.4c03376DOI Listing

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