Correction to: Nature Geoscience https://doi.org/10.1038/s41561-023-01169-4, published online 4 May 2023.

In the version of this article initially published, the amount of possibly formed Fe2O3 via additional redox disproportionation of Fe2+ during quenching in bridgmanite-enriched samples (run nos. OT2775 and OT2846) was incorrectly underestimated (i.e., 0.3–0.7 wt%), and we did not correct the Fe3+/ΣFe ratios of these two samples because of small amounts of Fe2O3 in comparison with the measured values of the samples (i.e., 4.26–5.02 wt%). The Fe2O3 amounts possibly formed upon quenching were re-estimated from the mass fraction of tiny metal droplets (i.e., 0.2 wt% for OT2775 and 0.5 wt% for OT2846) to be 0.6 wt% for OT2775 and 1.4 wt% for OT2846 assuming the reaction of 3FeO → Fe and Fe2O3. Accordingly, the revised Fe3+/ΣFe ratios of OT2775 and OT2846 are 0.378 and 0.351, respectively. Using these revised data, the required pressure derivative of bulk compressibility κ’ of FeO1.5 slightly changes from the original value of 1.4 to 1.5 to fit the experimental data. The change of κ′ of FeO1.5 slightly affects oxygen-fugacity profiles at high pressures above 20 GPa in Fig. 3. Fig. 2 and its caption and Fig. 3 have been updated. These corrections do not change the conclusion of the study and the authors apologize for any confusion for readers. It is noted that bright areas of back-scattered electron images identified as metal droplets may contain other minor phases, such as Ca-rich phase (i.e., former CaSiO3 perovskite). If this is the case, the area fraction of metal droplets and amounts of Fe2O3 possibly formed upon quenching are overestimated. Thus, the revised Fe3+/ΣFe ratios of OT2775 and OT2846 are likely lower bounds. Table 1 now contains both corrected data and measured original data of OT2775 and OT2846 for transparency.