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Tunable Charge Transport and Spin Dynamics in Two-Dimensional Conjugated Metal-Organic Frameworks.
Lu, Yang; Hu, Ziqi; Petkov, Petko; Fu, Shuai; Qi, Haoyuan; Huang, Chuanhui; Liu, Yannan; Huang, Xing; Wang, Mingchao; Zhang, Peng; Kaiser, Ute; Bonn, Mischa; Wang, Hai I; Samorì, Paolo; Coronado, Eugenio; Dong, Renhao; Feng, Xinliang.
Affiliation
  • Lu Y; Max Planck Institute of Microstructure Physics, 06120 Halle (Saale), Germany.
  • Hu Z; Center for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01067 Dresden, Germany.
  • Petkov P; Université de Strasbourg, CNRS, ISIS, UMR 7006, 8 Alleé Gaspard Monge, 67000 Strasbourg, France.
  • Fu S; Instituto de Ciencia Molecular (ICMol), Universitat de València, 46980 Paterna, Spain.
  • Qi H; Department of Materials Science and Engineering, CAS Key Laboratory of Materials for Energy Conversion, Anhui Laboratory of Advanced Photon Science and Technology, University of Science and Technology of China, 230026 Hefei, China.
  • Huang C; Faculty of Chemistry and Pharmacy, University of Sofia, 1164 Sofia, Bulgaria.
  • Liu Y; Center for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01067 Dresden, Germany.
  • Huang X; Max Planck Institute for Polymer Research, 55128 Mainz, Germany.
  • Wang M; Central Facility for Electron Microscopy, Electron Microscopy of Materials Science, Universität Ulm, 89081 Ulm, Germany.
  • Zhang P; Center for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01067 Dresden, Germany.
  • Kaiser U; Max Planck Institute of Microstructure Physics, 06120 Halle (Saale), Germany.
  • Bonn M; Max Planck Institute of Microstructure Physics, 06120 Halle (Saale), Germany.
  • Wang HI; Center for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01067 Dresden, Germany.
  • Samorì P; Center for Advancing Electronics Dresden and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01067 Dresden, Germany.
  • Coronado E; Central Facility for Electron Microscopy, Electron Microscopy of Materials Science, Universität Ulm, 89081 Ulm, Germany.
  • Dong R; Max Planck Institute for Polymer Research, 55128 Mainz, Germany.
  • Feng X; Max Planck Institute for Polymer Research, 55128 Mainz, Germany.
J Am Chem Soc ; 146(4): 2574-2582, 2024 Jan 31.
Article in En | MEDLINE | ID: mdl-38231138
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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos