The smelting of metallic iron has played a significant role in human civilization; however, conventional ironmaking processes re- main a leading contributor to greenhouse gas emissions, exacerbating global warming. Hydrogen-driven direct reduction (HyDR) of iron ore offers a sustainable alternative, leveraging the clean combustion of H2 to slash CO2 emissions. Nevertheless, HyDR involves complex, multi-step gas-solid transformations dictated by temperature: above 570°C, the reduction follows α-Fe2O3 → Fe3O4 → FeO → Fe, while below 570°C, the thermodynamic instability of FeO truncates the pathway to α-Fe2O3 → Fe3O4 → Fe, in accordance with the bulk Fe-O phase diagram [1-3]. While macroscopic characterization techniques such as thermogravimetric analysis (TGA) and high-resolution X-ray diffraction (XRD) are capable of tracking bulk phase transitions [4-6], they lack the spatial resolution to probe localized reaction dynamics at defects, grain boundaries, and reaction interfaces—critical features that govern solid-state diffusion pathways, nucleation barriers, and kinetic bottlenecks. Bridging this gap demands advanced in- situ techniques to visualize transient transformations and defect-mediated reduction mechanisms. Such insights are critical for optimizing HyDR efficiency and scalability in decarbonized steelmaking. Environmental transmission electron microscopy (ETEM) provides a unique platform to investigate local structural and inter- facial dynamics [7]. By introducing a reducing gas into the sample region while simultaneously capturing the atomic-scale evo- lution from the outermost surface to deeper layers, ETEM enables direct visualization of the reduction process of iron oxides. In this study, we employ ETEM to dynamically monitor the atomic-scale surface and interfacial structural evolution during H2-induced reduction of Fe3O4 and FeO, revealing the formation of an intermediate amorphous Fe phase. Our results demon- strate the critical role of surfaces and interfaces in the initial metallization process, offering new atomic-scale insights into the re- duction mechanisms of iron oxides. The fundamental insight has significant implications for metallurgy, thin-film fabrication, catalysis, and corrosion science.
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In-Situ Atomic-Scale Revelation of Amorphous Metallic Iron Formation during Hydrogen-Driven Reduction of Iron Oxides
The transition to hydrogen as a green reductant in metal production is critical for decarbonizing the metallurgical industry, yet atomic-scale mechanisms governing reduction pathways and phase evolution remain unresolved. Using in-situ environmental transmission electron microscopy, we identify a hidden pathway that reveals dynamic formation of amorphous metallic iron (Fe) during the hydrogen-driven reduction of ferrous oxides of Fe3O4 and FeO. Real-time imaging uncovers three coexisting transformation routes: (i) Fe3O4 → FeO, (ii) Fe3O4 → amorphous Fe, and (iii) FeO → amorphous Fe. The resulting amorphous Fe exhibits fluid-like mobility, enabling its rapid aggregation and crystallization into core-shell nanostructures, with a crystalline core enveloped by an amorphous shell. Complementary ab initio molecular dynamics simulations trace the amorphous Fe formation to interfacial strain at the metal/oxide interfaces, where large lattice mismatches destabilize the metal lattice during initial metallization. This interplay between thermodynamics and kinetics governs phase evolution: thermodynamics favors a self-limiting amorphous Fe overlayer, while rapid oxide reduction kinetics drives amorphous overgrowth. Our findings demonstrate that amorphous intermediates bypass rate-limiting crystalline steps, providing mechanistic insights to optimize H2-based processes for sustainable steelmaking. These insights bridge the gap between macroscopic process engineering and atomic-scale dynamics, with broader implications for catalysis and nanostructured material synthesis, where oxide reduction pathways critically shape functional phases and microstructures.
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- Award ID(s):
- 2303712
- PAR ID:
- 10680958
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- ACS Applied Materials & Interfaces
- Volume:
- 17
- Issue:
- 29
- ISSN:
- 1944-8244
- Page Range / eLocation ID:
- 42380 to 42393
- Subject(s) / Keyword(s):
- Hydrogen-driven direct reduction Amorphous Iron Fe3O4 FeO In-Situ Transmission Electron Microscopy Density Functional Theory
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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