4.7 Article

Optimized Anticorrosion of Polypyrrole Coating by Inverted-Electrode Strategy: Experimental and Molecular Dynamics Investigations

期刊

POLYMERS
卷 14, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/polym14071356

关键词

polypyrrole; electrodeposition; anodic protection; molecular dynamic; diffusion trajectory

资金

  1. Beijing Municipal Natural Science Foundation [2192016]
  2. National Natural Science Foundation of China [21606005]
  3. Support Project of High-level Teachers in Beijing Municipal Universities in the Period of 13th Five-year Plan [CITTCD201904042]
  4. Opening Project of Material Corrosion and Protection Key Laboratory of Sichuan Province [2021CL20]

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By employing an inverted-electrode strategy, a compact coating (PPy-I) with good adhesion, suitable thickness and conductivity was successfully deposited on copper surface to enhance the anticorrosion efficacy of electropolymerized polypyrrole (PPy). PPy-I demonstrated favorable protection for copper in artificial seawater (ASW) with lower water wettability. The higher density of PPy-I allowed it to retain efficient anticorrosion capacity on copper at elevated temperatures, which can be attributed to the tight coating architecture and electroactivity.
To improve the poor adhesion and the ensuing insufficient anticorrosion efficacy of electropolymerized polypyrrole (PPy) on copper surface, an inverted-electrode strategy was applied after the passivation procedure, for which the compact coating (PPy-I) was deposited on the substrate in a cathodic window. Morphological and physical characterizations revealed that PPy-I exerted satisfactory adhesion strength and suitable thickness and conductivity compared with the analogue prepared via the traditional protocol (PPy-T). Potentiodynamic polarization, electrochemical impedance spectroscopy and frequency modulation were employed to ascertain the propitious protection of PPy-I for copper in artificial seawater (ASW). Due to the dominant electroactivity, the PPy-I-coated sample possessed higher apparent current density and lower charge transfer resistance than its PPy-T-protected counterpart, which maintained the passivation of the substrate. Surface analysis also supported the viability of PPy-I for copper in ASW for a well-protected surface with inferior water wettability. Molecular dynamics simulations evidenced that PPy-I with the higher density retained efficient anticorrosion capacity on copper at elevated temperatures. Therein, the derived time-dependent spatial diffusion trajectories of ions were locally confined with low diffusion coefficients. Highly twisted pore passages and anodic protection behavior arising respectively from the tight coating architecture and electroactivity contributed to the adequate corrosion resistance of PPy-I-coated copper.

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