Oppositely Charged Ti3C2Tx MXene Membranes with 2D Nanofluidic Channels for Osmotic Energy Harvesting

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Li Ding
  • Dan Xiao
  • Zong Lu
  • Junjie Deng
  • Yanying Wei
  • Jürgen Caro
  • Haihui Wang

Externe Organisationen

  • South China University of Technology
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)8720-8726
Seitenumfang7
FachzeitschriftAngewandte Chemie - International Edition
Jahrgang59
Ausgabenummer22
Frühes Online-Datum16 Feb. 2020
PublikationsstatusVeröffentlicht - 15 Mai 2020

Abstract

Membrane-based reverse electrodialysis (RED) is considered as the most promising technique to harvest osmotic energy. However, the traditional membranes are limited by high internal resistance and low efficiency, resulting in undesirable power densities. Herein, we report the combination of oppositely charged Ti3C2Tx MXene membranes (MXMs) with confined 2D nanofluidic channels as high-performance osmotic power generators. The negatively or positively charged 2D MXene nanochannels exhibit typical surface-charge-governed ion transport and show excellent cation or anion selectivity. By mixing the artificial sea water (0.5 m NaCl) and river water (0.01 m NaCl), we obtain a maximum power density of ca. 4.6 Wm−2, higher than most of the state-of-the-art membrane-based osmotic power generators, and very close to the commercialization benchmark (5 Wm−2). Through connecting ten tandem MXM-RED stacks, the output voltage can reach up 1.66 V, which can directly power the electronic devices.

ASJC Scopus Sachgebiete

Zitieren

Oppositely Charged Ti3C2Tx MXene Membranes with 2D Nanofluidic Channels for Osmotic Energy Harvesting. / Ding, Li; Xiao, Dan; Lu, Zong et al.
in: Angewandte Chemie - International Edition, Jahrgang 59, Nr. 22, 15.05.2020, S. 8720-8726.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Ding L, Xiao D, Lu Z, Deng J, Wei Y, Caro J et al. Oppositely Charged Ti3C2Tx MXene Membranes with 2D Nanofluidic Channels for Osmotic Energy Harvesting. Angewandte Chemie - International Edition. 2020 Mai 15;59(22):8720-8726. Epub 2020 Feb 16. doi: 10.1002/anie.201915993, 10.1002/ange.201915993
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abstract = "Membrane-based reverse electrodialysis (RED) is considered as the most promising technique to harvest osmotic energy. However, the traditional membranes are limited by high internal resistance and low efficiency, resulting in undesirable power densities. Herein, we report the combination of oppositely charged Ti3C2Tx MXene membranes (MXMs) with confined 2D nanofluidic channels as high-performance osmotic power generators. The negatively or positively charged 2D MXene nanochannels exhibit typical surface-charge-governed ion transport and show excellent cation or anion selectivity. By mixing the artificial sea water (0.5 m NaCl) and river water (0.01 m NaCl), we obtain a maximum power density of ca. 4.6 Wm−2, higher than most of the state-of-the-art membrane-based osmotic power generators, and very close to the commercialization benchmark (5 Wm−2). Through connecting ten tandem MXM-RED stacks, the output voltage can reach up 1.66 V, which can directly power the electronic devices.",
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T1 - Oppositely Charged Ti3C2Tx MXene Membranes with 2D Nanofluidic Channels for Osmotic Energy Harvesting

AU - Ding, Li

AU - Xiao, Dan

AU - Lu, Zong

AU - Deng, Junjie

AU - Wei, Yanying

AU - Caro, Jürgen

AU - Wang, Haihui

N1 - Funding Information: This work acknowledges the funding from the Natural Science Foundation of China (21861132013, 21536005, 51621001), NSFC-DFG (GZ-678); China Postdoctoral Science Foundation (2019TQ0101, 2019M662920).

PY - 2020/5/15

Y1 - 2020/5/15

N2 - Membrane-based reverse electrodialysis (RED) is considered as the most promising technique to harvest osmotic energy. However, the traditional membranes are limited by high internal resistance and low efficiency, resulting in undesirable power densities. Herein, we report the combination of oppositely charged Ti3C2Tx MXene membranes (MXMs) with confined 2D nanofluidic channels as high-performance osmotic power generators. The negatively or positively charged 2D MXene nanochannels exhibit typical surface-charge-governed ion transport and show excellent cation or anion selectivity. By mixing the artificial sea water (0.5 m NaCl) and river water (0.01 m NaCl), we obtain a maximum power density of ca. 4.6 Wm−2, higher than most of the state-of-the-art membrane-based osmotic power generators, and very close to the commercialization benchmark (5 Wm−2). Through connecting ten tandem MXM-RED stacks, the output voltage can reach up 1.66 V, which can directly power the electronic devices.

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