Asymmetric Electrosorption in a Bio‐Inspired Reactor Enables Energy Efficient Ocean Carbon Removal

Y Yifang Zhu J Jundong Wang Y Yang Ou (Center of Electron Microscopy and State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) J Jay Fuhrman (Joint Global Change Research Institute University of Maryland and Pacific Northwest National Laboratory College Park Maryland MD USA) H Haodong Ji M Meng Lin Y Yandi Hu (Key Laboratory of Water and Sediment Sciences, Ministry of Education; College of Environmental Sciences and Engineering, Peking University) J Juan Liu K Kuichang Zuo H Huazhang Zhao (Key Laboratory of Water and Sediment Sciences, Ministry of Education; College of Environmental Sciences and Engineering, Peking University) Z Zishuai Zhang (The Key Laboratory of Water and Sediment Sciences Ministry of Education Peking University Haidian Beijing China)

Abstract

Abstract Ocean carbon removal represents a promising pathway for mitigating residual anthropogenic carbon dioxide (CO 2 ), yet existing methods are constrained by high energy demands and potential ecological risks. Here, inspired by the natural calcification process of corals, we present a bio‐inspired capacitive decarbonization (CDC) reactor that sequesters dissolved inorganic carbon (DIC) from seawater as CaCO 3 using only seawater‐derived Ca 2+ and renewable electricity. The CDC system integrates a Ca 2+ ‐selective electrode with a weak electric field to regulate ion transport and disrupt the hydration shell of Ca 2+ , enhancing its reaction with CO 3 2− . To address the limited concentration of CO 3 2− relative to Ca 2+ in seawater, we introduce an asymmetric electrosorption strategy to preferentially enrich CO 3 2− at the electrode interface, achieving a DIC conversion rate of up to 34% with an ultralow intrinsic electrochemical energy input of 2.5 kJ mol −1 CO 2 for the CDC reactor. The reactor exhibits stable continuous operation for over 100 h without fouling, enabled by spatially decoupled CaCO 3 precipitation. To mitigate the reduction in seawater alkalinity, we introduce a mineral‐assisted re‐alkalinization step that effectively restores pH and supports continued CO 2 absorption. A global integrated analysis model shows the CDC technology could remove up to 11–438 million tonnes of CO 2 by 2050–2100. This work demonstrates a scalable and low‐energy solution for durable ocean carbon removal.

Article Details

Volume / Issue Vol. 64, Issue 49
Published December 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

Y

Yifang Zhu

J

Jundong Wang

Y

Yang Ou

Center of Electron Microscopy and State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

J

Jay Fuhrman

Joint Global Change Research Institute University of Maryland and Pacific Northwest National Laboratory College Park Maryland MD USA

H

Haodong Ji

M

Meng Lin

Y

Yandi Hu

Key Laboratory of Water and Sediment Sciences, Ministry of Education; College of Environmental Sciences and Engineering, Peking University

J

Juan Liu

K

Kuichang Zuo

H

Huazhang Zhao

Key Laboratory of Water and Sediment Sciences, Ministry of Education; College of Environmental Sciences and Engineering, Peking University

Z

Zishuai Zhang

The Key Laboratory of Water and Sediment Sciences Ministry of Education Peking University Haidian Beijing China