Electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation

Abstract Selective ion transport underpins fundamental biological processes for efficient energy conversion and signal propagation. Mimicking these ‘ionics’ in synthetic nanofluidic channels has been increasingly promising for realizing self-sustained systems by harvesting clean energy from diverse...

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Main Authors: Zhuyuan Wang, Ting Hu, Mike Tebyetekerwa, Xiangkang Zeng, Fan Du, Yuan Kang, Xuefeng Li, Hao Zhang, Huanting Wang, Xiwang Zhang
Format: Article
Language:English
Published: Nature Portfolio 2024-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-47040-x
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author Zhuyuan Wang
Ting Hu
Mike Tebyetekerwa
Xiangkang Zeng
Fan Du
Yuan Kang
Xuefeng Li
Hao Zhang
Huanting Wang
Xiwang Zhang
author_facet Zhuyuan Wang
Ting Hu
Mike Tebyetekerwa
Xiangkang Zeng
Fan Du
Yuan Kang
Xuefeng Li
Hao Zhang
Huanting Wang
Xiwang Zhang
author_sort Zhuyuan Wang
collection DOAJ
description Abstract Selective ion transport underpins fundamental biological processes for efficient energy conversion and signal propagation. Mimicking these ‘ionics’ in synthetic nanofluidic channels has been increasingly promising for realizing self-sustained systems by harvesting clean energy from diverse environments, such as light, moisture, salinity gradient, etc. Here, we report a spatially nanoconfined ion separation strategy that enables harvesting electricity from CO2 adsorption. This breakthrough relies on the development of Nanosheet-Agarose Hydrogel (NAH) composite-based generators, wherein the oppositely charged ions are released in water-filled hydrogel channels upon adsorbing CO2. By tuning the ion size and ion-channel interactions, the released cations at the hundred-nanometer scale are spatially confined within the hydrogel network, while ångström-scale anions pass through unhindered. This leads to near-perfect anion/cation separation across the generator with a selectivity (D-/D+) of up to 1.8 × 106, allowing conversion into external electricity. With amplification by connecting multiple as-designed generators, the ion separation-induced electricity reaching 5 V is used to power electronic devices. This study introduces an effective spatial nanoconfinement strategy for widely demanded high-precision ion separation, encouraging a carbon-negative technique with simultaneous CO2 adsorption and energy generation.
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spelling doaj.art-0a9bfea9db684e47bfb0db80d5fe3beb2024-03-31T11:25:40ZengNature PortfolioNature Communications2041-17232024-03-011511910.1038/s41467-024-47040-xElectricity generation from carbon dioxide adsorption by spatially nanoconfined ion separationZhuyuan Wang0Ting Hu1Mike Tebyetekerwa2Xiangkang Zeng3Fan Du4Yuan Kang5Xuefeng Li6Hao Zhang7Huanting Wang8Xiwang Zhang9UQ Dow Centre for Sustainable Engineering Innovation, School of Chemical Engineering, The University of QueenslandDepartment of Chemical and Biological Engineering, Monash UniversityUQ Dow Centre for Sustainable Engineering Innovation, School of Chemical Engineering, The University of QueenslandUQ Dow Centre for Sustainable Engineering Innovation, School of Chemical Engineering, The University of QueenslandDepartment of Chemical and Biological Engineering, Monash UniversityDepartment of Chemical and Biological Engineering, Monash UniversityUQ Dow Centre for Sustainable Engineering Innovation, School of Chemical Engineering, The University of QueenslandUQ Dow Centre for Sustainable Engineering Innovation, School of Chemical Engineering, The University of QueenslandDepartment of Chemical and Biological Engineering, Monash UniversityUQ Dow Centre for Sustainable Engineering Innovation, School of Chemical Engineering, The University of QueenslandAbstract Selective ion transport underpins fundamental biological processes for efficient energy conversion and signal propagation. Mimicking these ‘ionics’ in synthetic nanofluidic channels has been increasingly promising for realizing self-sustained systems by harvesting clean energy from diverse environments, such as light, moisture, salinity gradient, etc. Here, we report a spatially nanoconfined ion separation strategy that enables harvesting electricity from CO2 adsorption. This breakthrough relies on the development of Nanosheet-Agarose Hydrogel (NAH) composite-based generators, wherein the oppositely charged ions are released in water-filled hydrogel channels upon adsorbing CO2. By tuning the ion size and ion-channel interactions, the released cations at the hundred-nanometer scale are spatially confined within the hydrogel network, while ångström-scale anions pass through unhindered. This leads to near-perfect anion/cation separation across the generator with a selectivity (D-/D+) of up to 1.8 × 106, allowing conversion into external electricity. With amplification by connecting multiple as-designed generators, the ion separation-induced electricity reaching 5 V is used to power electronic devices. This study introduces an effective spatial nanoconfinement strategy for widely demanded high-precision ion separation, encouraging a carbon-negative technique with simultaneous CO2 adsorption and energy generation.https://doi.org/10.1038/s41467-024-47040-x
spellingShingle Zhuyuan Wang
Ting Hu
Mike Tebyetekerwa
Xiangkang Zeng
Fan Du
Yuan Kang
Xuefeng Li
Hao Zhang
Huanting Wang
Xiwang Zhang
Electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation
Nature Communications
title Electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation
title_full Electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation
title_fullStr Electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation
title_full_unstemmed Electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation
title_short Electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation
title_sort electricity generation from carbon dioxide adsorption by spatially nanoconfined ion separation
url https://doi.org/10.1038/s41467-024-47040-x
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