Abstract
Direct air capture (DAC) represents a vital technology for atmospheric CO2 remediation, but few studies have tested catalysts at dilute atmospheric CO2 concentrations. Inspired by the carbonic anhydrase metalloenzyme, we report a catalytic DAC strategy employing robust zinc(II) enzyme mimics that enable efficient CO2 sequestration pathways. A catalyst-mediated CO2 hydration cycle in aqueous sorbents facilitates accelerated capture from dilute atmospheric air, thereby addressing the kinetic limitations observed in carbonate-based systems. Our developed complexes [ZnC1] and [ZnC2] enhance capture rates up to 2-fold at millimolar concentrations and improve the CO2 mass transfer by 40–60% in 1 M K2CO3 sorbent under ambient conditions. These bench-stable, earth-abundant zinc catalysts operate effectively under dilute CO2 concentrations, overcoming the kinetic limitations of conventional carbonate-based sorbents. Mechanistic studies support a biomimetic catalytic cycle that facilitates rapid CO2 conversion, demonstrating that a catalyst-assisted DAC can enable energy-efficient, scalable carbon capture technologies.
| Original language | English |
|---|---|
| Pages (from-to) | 5221-5232 |
| Number of pages | 12 |
| Journal | Energy and Fuels |
| Volume | 40 |
| Issue number | 10 |
| DOIs | |
| State | Published - Mar 12 2026 |
Bibliographical note
Publisher Copyright:© 2026 The Authors. Published by American Chemical Society
Funding
This material is based upon work partially supported by the Department of Energy under award number DE-FE0032255. Support was also received from the PPL Corporation, TotalEnergies, and the Electric Power Research Institute (EPRI).
| Funders | Funder number |
|---|---|
| Electric Power Research Institute, Louisville Gas & Electric | |
| Total S.A. | |
| PPL Corporation | |
| U.S. Department of Energy | DE-FE0032255 |
ASJC Scopus subject areas
- General Chemical Engineering
- Fuel Technology
- Energy Engineering and Power Technology
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