IronOxide_TC

Introduction

We conducted computational thermodynamic analyses using the CALPHAD (Calculation of Phase Diagrams) approach to study the phase equilibria involving iron, various iron oxide polymorphs, and gases for the PVD (Physical Vapor Deposition) synthesis. Our study comprises two types of Gibbs energy evaluations:

1. Full Equilibrium Calculations: These map out stable phases as functions of both temperature and oxygen activity.
2. Instantaneous Driving Force: This represents the energetic shift in the system when an infinitesimal amount of solid phase (either iron or an iron oxide) is deposited from a supersaturated gas phase. This was also examined as a function of temperature and oxygen activity.

We referenced the oxygen activity to that in the gas phase at each specified temperature, under standard atmospheric conditions. The PVD experiments are assumed to have been conducted at a constant level of oxygen activity, with the atmospheric conditions being a mixture of argon and oxygen.

Experimental Conditions

We labelled the plots with oxygen activities corresponding to the experimental conditions:

• BCC iron-forming condition: At an infinitesimal oxygen activity at 300°C.
• Experimental magnetite-forming condition: Corresponds to a volumetric flow rate ratio of 40/2 for argon and oxygen at 300°C.
• Experimental hematite-forming condition: Corresponds to a volumetric flow rate ratio of 40/10 for argon and oxygen at 25°C.

All PVD experiments were conducted at a pressure of 0.5 Pa (5 x 10^-3 mbar).

Databases and Calculations

We used the Gibbs energy assessments of BCC iron from the TCFE13 database, as well as hematite, magnetite, and wüstite, and the gas phase, from the SSUB5 database of Thermo-Calc. Parallelised calculations were performed via the tc-python API by Thermo-Calc.

Notebook and macro

• See IronOxide_TC_stoichiometric.ipynb for complete calculations and visualisations. It uses the free energy for oxides from the SSUB substance database. In this case, the oxides are treated as stoichiometric compounds. We should know the uncertainties regarding using the Gibbs energy extrapolated to the low-temperature regime.

• Some Thermo-Calc macros for console mode are included in the ./TC macro directory.

Visuals

Full Equilibrium phase diagram as a function of temperature and O activity

Instantaneous Driving force of depositing phases (from gas phase) as a function of temperature and O activity

Driving Force diagram: zoom in

Low oxygen activity condition: small dot shows the physical vapour deposition condition (./TC_macro/tc_O_activity.TCM).

High oxygen activity condition:

Maximum instantaneous driving force diagram.