Phase-controlled surface engineering of MoS₂/MXene heterostructures for enhanced capacitive deionization performance.
Saved in:
| Title: | Phase-controlled surface engineering of MoS₂/MXene heterostructures for enhanced capacitive deionization performance. |
|---|---|
| Authors: | Ho, Ying-Rong1 (AUTHOR), Hsieh, Cheng-En2 (AUTHOR), Huang, Jung-Jie1 (AUTHOR) jjhuang@asia.edu.tw |
| Source: | Surface & Coatings Technology. Jul2026, Vol. 532, pN.PAG-N.PAG. 1p. |
| Subjects: | Molybdenum disulfide, MXenes, Hydrothermal synthesis, Nanocomposite materials, Phase transitions, Saline water conversion, Electrode performance, Adsorption capacity |
| Abstract: | This study reports the strategic development of MoS 2 /MXene nanocomposites as high-efficiency electrodes for capacitive deionization (CDI) applications. The MXene synthesized via selective etching of MAX, provides a conductive, layered framework that facilitates rapid ion transport and expansive adsorption interfaces. To optimize electrochemical activity and structural integrity, layered MoS 2 was integrated into the MXene substrate through a high-pressure hydrothermal route. The influence of MoS 2 loading was systematically investigated by modulating the precursor molar ratios. Furthermore, nitrogen annealing at varying temperatures was employed to control the crystalline phase of MoS 2 , driving the transition from a metastable 1 T/2H mixed phase to a stable 2H phase, thereby enhancing both charge storage capacity and material durability. Experimental results demonstrate that optimized thermal treatment significantly improved the specific capacitance from 13.42 to 20.06 F/g, while the desalination efficiency increased from 4.63% to 10.86%. Notably, the composite electrode exhibited a robust salt adsorption capacity of 39.38 mg/g and maintained a high retention rate of 96.62% over 50 consecutive cycles. These findings highlight the potential of MoS 2 /MXene heterostructures as a superior material platform for next-generation, high-stability desalination technologies. • MoS 2 /MXene heterostructures synthesized by hydrothermal method. • MoS 2 phase transition from 1 T/2H to 2H after N 2 annealing at 850 °C. • High salt adsorption capacity (SAC) of 39.38 mg/g is achieved. • Excellent stability with 96.62% retention over 50 cycles. [ABSTRACT FROM AUTHOR] |
| Copyright of Surface & Coatings Technology is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: egs DbLabel: Engineering Source An: 194252947 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Phase-controlled surface engineering of MoS₂/MXene heterostructures for enhanced capacitive deionization performance. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ho%2C+Ying-Rong%22">Ho, Ying-Rong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hsieh%2C+Cheng-En%22">Hsieh, Cheng-En</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Huang%2C+Jung-Jie%22">Huang, Jung-Jie</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> jjhuang@asia.edu.tw</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Surface+%26+Coatings+Technology%22">Surface & Coatings Technology</searchLink>. Jul2026, Vol. 532, pN.PAG-N.PAG. 1p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Molybdenum+disulfide%22">Molybdenum disulfide</searchLink><br /><searchLink fieldCode="DE" term="%22MXenes%22">MXenes</searchLink><br /><searchLink fieldCode="DE" term="%22Hydrothermal+synthesis%22">Hydrothermal synthesis</searchLink><br /><searchLink fieldCode="DE" term="%22Nanocomposite+materials%22">Nanocomposite materials</searchLink><br /><searchLink fieldCode="DE" term="%22Phase+transitions%22">Phase transitions</searchLink><br /><searchLink fieldCode="DE" term="%22Saline+water+conversion%22">Saline water conversion</searchLink><br /><searchLink fieldCode="DE" term="%22Electrode+performance%22">Electrode performance</searchLink><br /><searchLink fieldCode="DE" term="%22Adsorption+capacity%22">Adsorption capacity</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: This study reports the strategic development of MoS 2 /MXene nanocomposites as high-efficiency electrodes for capacitive deionization (CDI) applications. The MXene synthesized via selective etching of MAX, provides a conductive, layered framework that facilitates rapid ion transport and expansive adsorption interfaces. To optimize electrochemical activity and structural integrity, layered MoS 2 was integrated into the MXene substrate through a high-pressure hydrothermal route. The influence of MoS 2 loading was systematically investigated by modulating the precursor molar ratios. Furthermore, nitrogen annealing at varying temperatures was employed to control the crystalline phase of MoS 2 , driving the transition from a metastable 1 T/2H mixed phase to a stable 2H phase, thereby enhancing both charge storage capacity and material durability. Experimental results demonstrate that optimized thermal treatment significantly improved the specific capacitance from 13.42 to 20.06 F/g, while the desalination efficiency increased from 4.63% to 10.86%. Notably, the composite electrode exhibited a robust salt adsorption capacity of 39.38 mg/g and maintained a high retention rate of 96.62% over 50 consecutive cycles. These findings highlight the potential of MoS 2 /MXene heterostructures as a superior material platform for next-generation, high-stability desalination technologies. • MoS 2 /MXene heterostructures synthesized by hydrothermal method. • MoS 2 phase transition from 1 T/2H to 2H after N 2 annealing at 850 °C. • High salt adsorption capacity (SAC) of 39.38 mg/g is achieved. • Excellent stability with 96.62% retention over 50 cycles. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Surface & Coatings Technology is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=194252947 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.surfcoat.2026.133616 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: N.PAG Subjects: – SubjectFull: Molybdenum disulfide Type: general – SubjectFull: MXenes Type: general – SubjectFull: Hydrothermal synthesis Type: general – SubjectFull: Nanocomposite materials Type: general – SubjectFull: Phase transitions Type: general – SubjectFull: Saline water conversion Type: general – SubjectFull: Electrode performance Type: general – SubjectFull: Adsorption capacity Type: general Titles: – TitleFull: Phase-controlled surface engineering of MoS₂/MXene heterostructures for enhanced capacitive deionization performance. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ho, Ying-Rong – PersonEntity: Name: NameFull: Hsieh, Cheng-En – PersonEntity: Name: NameFull: Huang, Jung-Jie IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 07 Text: Jul2026 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 02578972 Numbering: – Type: volume Value: 532 Titles: – TitleFull: Surface & Coatings Technology Type: main |
| ResultId | 1 |