Jie Li, Zhen Xu, Yang He, Qianxi Yang, Haoyang Pan, Yudi Wang, Xin Li, Huamei Chen, Yansong Wang, Wenjie Dong, Shimin Hou, Xiong Zhou, Qian Shen, Song Gao, Kai Wu, Yongfeng Wang, Yajie Zhang
{"title":"磁性DyPc2分子与超导Pb(111)表面相互作用的检测与操纵","authors":"Jie Li, Zhen Xu, Yang He, Qianxi Yang, Haoyang Pan, Yudi Wang, Xin Li, Huamei Chen, Yansong Wang, Wenjie Dong, Shimin Hou, Xiong Zhou, Qian Shen, Song Gao, Kai Wu, Yongfeng Wang, Yajie Zhang","doi":"10.1002/admi.202400788","DOIUrl":null,"url":null,"abstract":"<p>Lanthanide double-decker phthalocyanine (LnPc<sub>2</sub>) complexes are highly coveted for their prospective uses in ultrahigh-density data storage and quantum computing. Notably, the quantum spin systems comprising these complexes and superconducting substrates exhibit unique quantum magnetic interactions. Through scanning tunneling microscopy (STM) and spectroscopy (STS) experiments, the interaction between the magnetic double-decker DyPc<sub>2</sub> molecules and the superconducting Pb(111) substrate is investigated. Three distinct adsorption patterns of DyPc<sub>2</sub> on Pb(111) are experimentally observed. Combined with DFT calculations, it is found that the ligand spin of the normal DyPc<sub>2</sub> molecules in the self-assembled monolayer (SAM) is quenched, which is attributed to strong charge transfer from Pb(111). However, special DyPc<sub>2</sub> molecules embedded in the SAM maintain ligand spin due to weak charge transfer, forming a complex quantum spin system with the superconducting substrate. Similarly, DyPc<sub>2</sub> molecules located on the second layer exhibit the same behavior. Under zero magnetic field, the Yu–Shiba–Rusinov (YSR) resonances are observed within the superconducting energy gap of both spin quantum systems. The Kondo resonance and the superconducting pairing occur at similar energy scales, indicating their coexistence and competition. This ultimately results in a Kondo-screened state. By controlling the sample bias, the special molecule can be switched to a normal molecule.</p>","PeriodicalId":115,"journal":{"name":"Advanced Materials Interfaces","volume":"12 10","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admi.202400788","citationCount":"0","resultStr":"{\"title\":\"Detection and Manipulation of Interaction Between Magnetic DyPc2 Molecules and Superconducting Pb(111) Surface\",\"authors\":\"Jie Li, Zhen Xu, Yang He, Qianxi Yang, Haoyang Pan, Yudi Wang, Xin Li, Huamei Chen, Yansong Wang, Wenjie Dong, Shimin Hou, Xiong Zhou, Qian Shen, Song Gao, Kai Wu, Yongfeng Wang, Yajie Zhang\",\"doi\":\"10.1002/admi.202400788\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Lanthanide double-decker phthalocyanine (LnPc<sub>2</sub>) complexes are highly coveted for their prospective uses in ultrahigh-density data storage and quantum computing. Notably, the quantum spin systems comprising these complexes and superconducting substrates exhibit unique quantum magnetic interactions. Through scanning tunneling microscopy (STM) and spectroscopy (STS) experiments, the interaction between the magnetic double-decker DyPc<sub>2</sub> molecules and the superconducting Pb(111) substrate is investigated. Three distinct adsorption patterns of DyPc<sub>2</sub> on Pb(111) are experimentally observed. Combined with DFT calculations, it is found that the ligand spin of the normal DyPc<sub>2</sub> molecules in the self-assembled monolayer (SAM) is quenched, which is attributed to strong charge transfer from Pb(111). However, special DyPc<sub>2</sub> molecules embedded in the SAM maintain ligand spin due to weak charge transfer, forming a complex quantum spin system with the superconducting substrate. Similarly, DyPc<sub>2</sub> molecules located on the second layer exhibit the same behavior. Under zero magnetic field, the Yu–Shiba–Rusinov (YSR) resonances are observed within the superconducting energy gap of both spin quantum systems. The Kondo resonance and the superconducting pairing occur at similar energy scales, indicating their coexistence and competition. This ultimately results in a Kondo-screened state. 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Detection and Manipulation of Interaction Between Magnetic DyPc2 Molecules and Superconducting Pb(111) Surface
Lanthanide double-decker phthalocyanine (LnPc2) complexes are highly coveted for their prospective uses in ultrahigh-density data storage and quantum computing. Notably, the quantum spin systems comprising these complexes and superconducting substrates exhibit unique quantum magnetic interactions. Through scanning tunneling microscopy (STM) and spectroscopy (STS) experiments, the interaction between the magnetic double-decker DyPc2 molecules and the superconducting Pb(111) substrate is investigated. Three distinct adsorption patterns of DyPc2 on Pb(111) are experimentally observed. Combined with DFT calculations, it is found that the ligand spin of the normal DyPc2 molecules in the self-assembled monolayer (SAM) is quenched, which is attributed to strong charge transfer from Pb(111). However, special DyPc2 molecules embedded in the SAM maintain ligand spin due to weak charge transfer, forming a complex quantum spin system with the superconducting substrate. Similarly, DyPc2 molecules located on the second layer exhibit the same behavior. Under zero magnetic field, the Yu–Shiba–Rusinov (YSR) resonances are observed within the superconducting energy gap of both spin quantum systems. The Kondo resonance and the superconducting pairing occur at similar energy scales, indicating their coexistence and competition. This ultimately results in a Kondo-screened state. By controlling the sample bias, the special molecule can be switched to a normal molecule.
期刊介绍:
Advanced Materials Interfaces publishes top-level research on interface technologies and effects. Considering any interface formed between solids, liquids, and gases, the journal ensures an interdisciplinary blend of physics, chemistry, materials science, and life sciences. Advanced Materials Interfaces was launched in 2014 and received an Impact Factor of 4.834 in 2018.
The scope of Advanced Materials Interfaces is dedicated to interfaces and surfaces that play an essential role in virtually all materials and devices. Physics, chemistry, materials science and life sciences blend to encourage new, cross-pollinating ideas, which will drive forward our understanding of the processes at the interface.
Advanced Materials Interfaces covers all topics in interface-related research:
Oil / water separation,
Applications of nanostructured materials,
2D materials and heterostructures,
Surfaces and interfaces in organic electronic devices,
Catalysis and membranes,
Self-assembly and nanopatterned surfaces,
Composite and coating materials,
Biointerfaces for technical and medical applications.
Advanced Materials Interfaces provides a forum for topics on surface and interface science with a wide choice of formats: Reviews, Full Papers, and Communications, as well as Progress Reports and Research News.