AI Article Synopsis

  • * Researchers developed new volatile Ir(I)-1,5-cyclooctadiene complexes with specialized ligands to enhance the deposition process and improve film quality.
  • * The resulting iridium films demonstrated excellent electrochemical performance, achieving low overpotentials for hydrogen evolution reaction, indicating their potential for large-scale practical applications.

Article Abstract

Thin films of iridium can be utilized in a wide range of applications and are particularly interesting for catalytic transformations. For the scalable deposition of functional Ir thin films, metalorganic chemical vapor deposition (MOCVD) is the method of choice, for which organometallic precursors that embody a high volatility and thermal stability need to be specifically tailored. Herein, we report the synthesis, analysis, and evaluation of new volatile Ir(I)-1,5-cyclooctadiene complexes bearing all-nitrogen coordinating guanidinate (,'-diisopropyl-2-dimethylamido-guanidinate (DPDMG)), amidinate (,'-diisopropyl-amidinate (DPAMD)), and formamidinate (,'-diisopropyl-formamidinate (DPfAMD)) ligands. The amidinate-based Ir complex [Ir(COD)(DPAMD)] together with O was implemented in MOCVD experiments resulting in highly crystalline, dense, and conductive Ir films on a variety of substrate materials. The Ir deposits achieved outstanding electrochemical performance with overpotentials in the range of 50 mV at -10 mA·cm for catalytic hydrogen evolution reaction (HER) in acidic solution. The ability to deposit Ir layers via MOCVD exhibiting promising functional properties is a significant step toward large-scale applications.

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Source
http://dx.doi.org/10.1021/acsami.2c13865DOI Listing

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