Tunable Charge Transport and Spin Dynamics in Two-Dimensional Conjugated Metal-Organic Frameworks

  • Yang Lu
  • , Ziqi Hu
  • , Petko Petkov
  • , Shuai Fu
  • , Haoyuan Qi
  • , Chuanhui Huang
  • , Yannan Liu
  • , Xing Huang
  • , Mingchao Wang
  • , Peng Zhang
  • , Ute Kaiser
  • , Mischa Bonn
  • , Hai I. Wang
  • , Paolo Samorì
  • , Eugenio Coronado*
  • , Renhao Dong*
  • , Xinliang Feng*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) have attracted increasing interest in electronics due to their (semi)conducting properties. Charge-neutral 2D c-MOFs also possess persistent organic radicals that can be viewed as spin-concentrated arrays, affording new opportunities for spintronics. However, the strong π-interaction between neighboring layers of layer-stacked 2D c-MOFs annihilates active spin centers and significantly accelerates spin relaxation, severely limiting their potential as spin qubits. Herein, we report the precise tuning of the charge transport and spin dynamics in 2D c-MOFs via the control of interlayer stacking. The introduction of bulky side groups on the conjugated ligands enables a significant dislocation of the 2D c-MOFs layers from serrated stacking to staggered stacking, thereby spatially weakening the interlayer interactions. As a consequence, the electrical conductivity of 2D c-MOFs decreases by 6 orders of magnitude, while the spin density achieves more than a 30-fold increase and the spin-lattice relaxation time (T1) is increased up to ∼60 μs, hence being superior to the reference 2D c-MOFs with compact stackings whose spin relaxation is too fast to be detected. Spin dynamics results also reveal that spinless polaron pairs or bipolarons play critical roles in the charge transport of these 2D c-MOFs. Our strategy provides a bottom-up approach for enlarging spin dynamics in 2D c-MOFs, opening up pathways for developing MOF-based spintronics.

Original languageEnglish
Pages (from-to)2574-2582
Number of pages9
JournalJournal of the American Chemical Society
Volume146
Issue number4
Early online date17 Jan 2024
DOIs
Publication statusPublished - 31 Jan 2024

Bibliographical note

Publisher Copyright:
© 2024 American Chemical Society

Funding

FundersFunder number
Center of Advancing Electronics Dresden
Dresden Center for Nanoanalysis
European Union-NextGenerationEU
FC2DMOF819698, 852909
Foundation Jean-Marie Lehn
IdEx UnistraANR-10-IDEX-0002
Interdisciplinary Thematic Institute SysChem
National Recovery and Resilience Plan of the Republic of BulgariaBG-RRP-2.004-0008
H2020 Marie Skłodowska-Curie ActionsGA-101103585
H2020 Marie Skłodowska-Curie Actions
Wissenschaftsrat
European Research Council
Deutsche ForschungsgemeinschaftRTG 2861, CRC-1415, 417590517, 491865171
Deutsche Forschungsgemeinschaft
National Natural Science Foundation of China22272092
National Natural Science Foundation of China
Technische Universität Dresden
Université de Strasbourg
Institut universitaire de France
Natural Science Foundation of Shandong ProvinceZR2023JQ005
Natural Science Foundation of Shandong Province
Taishan Scholar Project of Shandong Provincetsqn201909047
Taishan Scholar Project of Shandong Province

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