Molecularly bridged design of an electron-delocalized dual redox-active organic electrode for high-efficiency capacitive deionization and water treatment

Capacitive deionization (CDI) is emerging as a promising technology for efficient water treatment, where the electrochemical performance is strongly influenced by the activity of electrode materials. Among these, faradaic organic electrodes with pseudocapacitive behavior offer great potential but remain limited due to insufficient redox-active sites and poor electron affinity, factors that constrain their ion adsorption capacity and desalination rate. In this study, we present a novel electron-delocalized organic molecular architecture, PTAP, which features a rigid conjugated backbone and dual redox-active centers located at C[double bond, length as m-dash]N and C[double bond, length as m-dash]O coordination sites. The molecular structure, optimized <i>via</i> extensive π-electron delocalization and a narrow HOMO-LUMO energy gap, significantly enhances Na<sup>+</sup> adsorption kinetics and facilitates efficient charge carrier transport. A combination of comprehensive experimental techniques and density functional theory (DFT) calculations was employed to elucidate the Na<sup>+</sup> electro-adsorption pathways and identify the active redox moieties. The resulting PTAP-integrated CDI device exhibited outstanding desalination performance, achieving an exceptionally high salt removal capacity of 91.50 mg g<sup>-1</sup>-far exceeding that of conventional organic-electrode CDI systems (typically < 60 mg g<sup>-1</sup>)-and a rapid removal rate of 3.05 mg g<sup>-1</sup> min<sup>-1</sup> at 1.2 V, while maintaining excellent cycling stability (∼95.55% retention over 100 cycles). Furthermore, a multi-module CDI system incorporating PTAP electrodes was developed, demonstrating high desalination efficiency in hypersaline environments. This system also enabled preliminary exploration of sustainable real-world applications, including dye-contaminated wastewater remediation and energy harvesting, underscoring the versatility and transformative potential of PTAP-based CDI technology.

Authors

Institutions

Publication Details

Journal
Chemical Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5sc03868e
Citations
1
Primary Topic
Membrane-based Ion Separation Techniques
Type
article
Field-Weighted Citation Impact
0.67

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Molecularly bridged design of an electron-delocalized dual redox-active organic electrode for high-efficiency capacitive deionization and water treatment

Minjie Shi, Zhiyong Han, Can Cui, Jun Yang et al.
1 citations
Chemical Science
Membrane-based Ion Separation Techniques
0.67
article

Molecularly bridged design of an electron-delocalized dual redox-active organic electrode for high-efficiency capacitive deionization and water treatment

Minjie Shi, Zhiyong Han, Can Cui, Jun Yang, Mugilan Narayanasamy, Edison Huixiang Ang, Lei Ke, H. Qiu, Xinyue Zhang
article en
1 citations

Abstract

Capacitive deionization (CDI) is emerging as a promising technology for efficient water treatment, where the electrochemical performance is strongly influenced by the activity of electrode materials. Among these, faradaic organic electrodes with pseudocapacitive behavior offer great potential but remain limited due to insufficient redox-active sites and poor electron affinity, factors that constrain their ion adsorption capacity and desalination rate. In this study, we present a novel electron-delocalized organic molecular architecture, PTAP, which features a rigid conjugated backbone and dual redox-active centers located at C[double bond, length as m-dash]N and C[double bond, length as m-dash]O coordination sites. The molecular structure, optimized <i>via</i> extensive π-electron delocalization and a narrow HOMO-LUMO energy gap, significantly enhances Na<sup>+</sup> adsorption kinetics and facilitates efficient charge carrier transport. A combination of comprehensive experimental techniques and density functional theory (DFT) calculations was employed to elucidate the Na<sup>+</sup> electro-adsorption pathways and identify the active redox moieties. The resulting PTAP-integrated CDI device exhibited outstanding desalination performance, achieving an exceptionally high salt removal capacity of 91.50 mg g<sup>-1</sup>-far exceeding that of conventional organic-electrode CDI systems (typically < 60 mg g<sup>-1</sup>)-and a rapid removal rate of 3.05 mg g<sup>-1</sup> min<sup>-1</sup> at 1.2 V, while maintaining excellent cycling stability (∼95.55% retention over 100 cycles). Furthermore, a multi-module CDI system incorporating PTAP electrodes was developed, demonstrating high desalination efficiency in hypersaline environments. This system also enabled preliminary exploration of sustainable real-world applications, including dye-contaminated wastewater remediation and energy harvesting, underscoring the versatility and transformative potential of PTAP-based CDI technology.

Chemical ScienceVol. 16(33)
Nanyang Technological University (SG), University of Limerick (IE), Jiangsu Changjiang Electronics Technology (China) (CN), Jiangsu University of Science and Technology (CN)
Ministry of Education - Singapore, National Natural Science Foundation of China, Government of Jiangsu Province, Natural Science Foundation of Jiangsu Province, National Institute of Education
Clean water and sanitation
Openalex Percentile: Top 29%
Membrane-based Ion Separation Techniques
0.67
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.