Fabrication of spin-1/2 Heisenberg antiferromagnetic chains via combined on-surface synthesis and reduction for spinon detection
Related Articles
Switching on and off the spin polarization of the conduction band in antiferromagnetic bilayer transistors
Antiferromagnetic conductors with suitably broken spatial symmetries host spin-polarized bands, which lead to transport phenomena commonly observed in metallic ferromagnets. In bulk materials, it is the given crystalline structure that determines whether symmetries are broken and spin-polarized bands are present. Here we show that, in the two-dimensional limit, an electric field can control the relevant symmetries. To this end, we fabricate a double-gate transistor based on bilayers of van der Waals antiferromagnetic semiconductor CrPS4 and show how a perpendicular electric displacement field can switch the spin polarization of the conduction band on and off. Because conduction band states with opposite spin polarizations are hosted in the different layers and are spatially separated, these devices also give control over the magnetization of the electrons that are accumulated electrostatically. Our experiments show that double-gated CrPS4 transistors provide a viable platform to create gate-induced conductors with near unity spin polarization at the Fermi level, as well as devices with a full electrostatic control of the total magnetization of the system.
Probing the weak limit of magnetocrystalline anisotropy through a spin‒flop transition in the van der Waals antiferromagnet CrPS4
The influence of magnetocrystalline anisotropy (MCA) on antiferromagnetism is elucidated through the characterization of the spin‒flop transition. However, due to a lack of suitable candidates for investigation, a detailed understanding of the preservation of the spin‒flop transition in the presence of low MCA energy remains elusive. In this study, we introduce CrPS4, which is a two-dimensional van der Waals antiferromagnet, as an ideal system to explore the exceedingly weak limit of the thermally-evolved MCA energy. By employing a uniaxially anisotropic spin model and fitting it to the experimental magnetic properties, we quantify the MCA energy and identify the discernible spin configurations in different magnetic phases. Notably, even at the limit of extremely weak MCA, with a mere 0.12% of the interlayer antiferromagnetic exchange interaction at T = 33 K, which is slightly below the Néel temperature (TN) of 38 K, the spin‒flop transition remains intact. We further establish a direct correlation between the visualized spin arrangements and the progressive reversal of magnetic torque induced by rotating magnetic fields. This analysis reveals the essential role of MCA in antiferromagnetism, thus extending our understanding to previously undetected limits and providing valuable insights for the development of spin-processing functionalities based on van der Waals magnets.
Spin-state effect on the efficiency of a post-synthetic modification reaction on a spin crossover complex
The spin state of a metal center significantly influences the catalytic activity of its complex, a phenomenon so crucial that it has led to the dedicated field of spin catalysis. Here we investigate the effect of the spin state of an iron-based metal complex on the organic reactivity of its ligands. Specifically, we examined the post-synthetic modification of the spin crossover (SCO) complex [Fe(NH2trz)3](NO3)2 with p-anisaldehyde. A series of experiments were performed to study the transformation of the amino groups depending on the spin state of the metal. Owing to the wide thermal hysteresis loop of the SCO complex, both spin states were compared under identical conditions. The results revealed that the high-spin state led to the formation of 1.34 times more imine functional groups than the low-spin state, we propose that this arises from the different interactions between the solvent and the SCO at the different spin states.
First-principles and machine-learning approaches for interpreting and predicting the properties of MXenes
MXenes are a versatile family of 2D inorganic materials with applications in energy storage, shielding, sensing, and catalysis. This review highlights computational studies using density functional theory and machine-learning approaches to explore their structure (stacking, functionalization, doping), properties (electronic, mechanical, magnetic), and application potential. Key advances and challenges are critically examined, offering insights into applying computational research to transition these materials from the lab to practical use.
Flexible micromachined ultrasound transducers (MUTs) for biomedical applications
The use of bulk piezoelectric transducer arrays in medical imaging is a well-established technology that operates based on thickness mode piezoelectric vibration. Meanwhile, advancements in fabrication techniques have led to the emergence of micromachined alternatives, namely, piezoelectric micromachined ultrasound transducer (PMUT) and capacitive micromachined ultrasound transducer (CMUT). These devices operate in flexural mode using piezoelectric thin films and electrostatic forces, respectively. In addition, the development of flexible ultrasound transducers based on these principles has opened up new possibilities for biomedical applications, including biomedical imaging, sensing, and stimulation. This review provides a detailed discussion of the need for flexible micromachined ultrasound transducers (MUTs) and potential applications, their specifications, materials, fabrication, and electronics integration. Specifically, the review covers fabrication approaches and compares the performance specifications of flexible PMUTs and CMUTs, including resonance frequency, sensitivity, flexibility, and other relevant factors. Finally, the review concludes with an outlook on the challenges and opportunities associated with the realization of efficient MUTs with high performance and flexibility.
Responses