Pressure-induced redox reversal of iron and the distribution of elements in deep Earth

X Xiaoli Wang (Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX, USA.) X Xiaolei Feng (School of Materials Science and Engineering, Nanyang Technological University) J Jianfu Li (School of Physics and Electronic Information, Yantai University) Y Yang Lv (State Key Laboratory of Coordination Chemistry, Key Laboratory of Mesoscopic Chemistry of MOE, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering) A Austin Ellis S Samantha Scott (Department of Chemistry and Biochemistry, California State University) A Abhiyan Pandit (Department of Chemistry and Biochemistry, California State University) D Dalar Khodagholian (Department of Chemistry and Biochemistry, California State University) R Russell J. Hemley (Department of Physics, University of Illinois Chicago) M Matthew G. Jackson (Department of Earth Science, University of California Santa Barbara) F Frank Spera (Department of Earth Science, University of California Santa Barbara) S Simon A. T. Redfern (Asian School of the Environment, Nanyang Technological University) M Maosheng Miao

Abstract

We demonstrate a remarkable change in the chemical bonding of iron under pressure that underlies the distribution of elements in the Earth’s mantle and core. Using a massive-scale, first-principles study, we show that while reacting with p -block elements under increasing pressure from ambient to Earth core conditions, iron tends to reverse its redox nature, changing from an electron donor (reductant) to an electron acceptor (oxidant), and oxidizes many p -block elements. Such reverse redox propensity significantly impacts the stoichiometries, bond types and strengths, structures, and properties of iron compounds under deep planetary conditions. This change transforms many p- block elements (conventionally labeled lithophile or chalcophile) into highly siderophile species. The chemical binding strengths with iron show an inverse correlation with the depletion of p -block elements in the silicate Earth. Furthermore, silicon shows a distinct anomaly in its bonding to iron, which suggests silicon may readily be incorporated into Earth’s core.

Article Details

Volume / Issue Vol. 122, Issue 46
Published November 18, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (13)

X

Xiaoli Wang

Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX, USA.

X

Xiaolei Feng

School of Materials Science and Engineering, Nanyang Technological University

J

Jianfu Li

School of Physics and Electronic Information, Yantai University

Y

Yang Lv

State Key Laboratory of Coordination Chemistry, Key Laboratory of Mesoscopic Chemistry of MOE, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering

A

Austin Ellis

S

Samantha Scott

Department of Chemistry and Biochemistry, California State University

A

Abhiyan Pandit

Department of Chemistry and Biochemistry, California State University

D

Dalar Khodagholian

Department of Chemistry and Biochemistry, California State University

R

Russell J. Hemley

Department of Physics, University of Illinois Chicago

M

Matthew G. Jackson

Department of Earth Science, University of California Santa Barbara

F

Frank Spera

Department of Earth Science, University of California Santa Barbara

S

Simon A. T. Redfern

Asian School of the Environment, Nanyang Technological University

M

Maosheng Miao