合金
催化作用
氧化物
材料科学
氧化还原
化学工程
金属
微观结构
冶金
杠杆(统计)
动能
生产(经济)
多相催化
温室气体
动力学
纳米技术
过渡金属
无机化学
作者
Xinren Chen,Baptiste Bienvenu,Tingting Yang,Baptiste Gault,Shaolou Wei,Xuyang Zhou,Dierk Raabe
标识
DOI:10.1038/s44160-026-01086-5
摘要
Abstract Metal production causes 10% of global greenhouse gas emissions, with most metals extracted from oxide ores via fossil-based pyrometallurgy, including melting. Solid-state hydrogen-driven redox reduction is not only a sustainable alternative, but can also be used to integrate reduction, in situ alloying of mixed oxides and microstructure design in one single process. Upon co-reduction of a Fe 2 O 3 –NiO mixture with hydrogen, we report a distinct type of solid–solid catalytic interaction between pre-reduced metal (Ni) and a transient oxide (FeO). This interaction accelerates hydrogen-based reduction by a factor of at least two, highlighting its potential relevance for improving reduction kinetics in hydrogen-based ironmaking and alloy production. Specifically, during hydrogen-driven co-reduction of Fe 2 O 3 and NiO, Ni partitioning takes place across metal–oxide interfaces, driven by interface dynamics, during which restructuring continuously regenerates the catalytic sites that promote H 2 spillover. These findings show that hydrogen-based alloy production is not only more sustainable than fossil-based practices, but can leverage kinetic and commercial advantages through solid–solid catalytic effects.
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