The intricate interplay between non-trivial topology and magnetism in two-dimensional materials can lead to the emergence of interesting phenomena such as the quantum anomalous Hall effect. Here we investigate the quantum transport of both bulk crystal and exfoliated MnBi 2 Te 4 flakes in a field-effect transistor geometry. For the six septuple-layer device tuned into the insulating regime, we observe a large longitudinal resistance and zero Hall plateau, which are characteristics of an axion insulator state. The robust axion insulator state occurs in zero magnetic field, over a wide magnetic-field range and at relatively high temperatures. Moreover, a moderate magnetic field drives a quantum phase transition from the axion insulator phase to a Chern insulator phase with zero longitudinal resistance and quantized Hall resistance h/e 2 , where h is Planck's constant and e is electron charge. Our results pave the way for using even-number septuple-layer MnBi 2 Te 4 to realize the quantized topological magnetoelectric effect and axion electrodynamics in condensed matter systems. Finding novel topological quantum matter and topological phase transitions has been a central theme in modern physics and mate rial science. An outstanding example is the quantum anomalous Hall (QAH) effect, which was realized in magnetically doped topo logical insulators (TIs) in the absence of magnetic field 1-6. The axion insulator is another exotic topological phase that has zero Chern number but a finite topological Chern-Simons term 7. It was put forward as a promising platform for exploring the Majorana edge modes, quantized topological magnetoelectric coupling and axion electrodynamics in condensed matter 7-12. Previous attempts to con struct the axion insulator phase were mainly based on fabricating heterostructures of QAH films with different coercive fields 13-15 , which require complex epitaxial growth of magnetically doped TIs, and transport measurements at ultralow temperatures and finite magnetic fields. There is an urgent need for finding a stoichiometric material that can achieve a robust axion insulator state in zero magnetic field and high temperatures. Recently, the layered van der Waals compound MnBi 2 Te 4 has been theoretically predicted and experimentally verified to be a TI with interlayer antiferromagnetic (AFM) order 16-26. It is a rare stoichiometric material with coexisting topology and mag netism, and thus represents a perfect building block for complex topological-magnetic structures. Interestingly, it naturally fulfils
Understanding molecular structures of interfacial peptides and proteins impacts many research fields by guiding the advancement of biocompatible materials, new and improved marine antifouling coatings, ultrasensitive and highly specific biosensors and biochips, therapies for diseases related to protein amyloid formation, and knowledge on mechanisms for various membrane proteins and their interactions with ligands. Developing methods for measuring such unique systems, as well as elucidating the structure and function relationship of such biomolecules, has been the goal of our lab at the University of Michigan. We have made substantial progress to develop sum frequency generation (SFG) vibrational spectroscopy into a powerful technique to study interfacial peptides and proteins, which lays a foundation to obtain unique and valuable insights when using SFG to probe various biologically relevant systems at the solid/liquid interface in situ in real time. One highlighting feature of this Account is the demonstration of the power of combining SFG with other techniques and methods such as ATR-FTIR, surface engineering, MD simulation, liquid crystal sensing, and isotope labeling in order to study peptides and proteins at interfaces. It is necessary to emphasize that SFG plays a major role in these studies, while other techniques and methods are supplemental. The central role of SFG is to provide critical information on interfacial peptide and protein structure (e.g., conformation and orientation) in order to elucidate how surface engineering (e.g., to vary the structure) can ultimately affect surface function (e.g., to optimize the activity). This Account focuses on the most significant recent progress in research on interfacial peptides and proteins carried out by our group including (1) the development of SFG analysis methods to determine orientations of regular as well as disrupted secondary structures, and the successful demonstration and application of an isotope labeling method with SFG to probe the detailed local structure and microenvironment of peptides at buried interfaces, (2) systematic research on cell membrane associated peptides and proteins including antimicrobial peptides, cell penetrating peptides, G proteins, and other membrane proteins, discussing the factors that influence interfacial peptide and protein structures such as lipid charge, membrane fluidity, and biomolecule solution concentration, and (3) in-depth discussion on solid surface immobilized antimicrobial peptides and enzymes. The effects of immobilization method, substrate surface, immobilization site on the peptide or protein, and surrounding environment are presented. Several examples leading to high impact new research are also briefly introduced: The orientation change of alamethicin detected while varying the model cell membrane potential demonstrates the feasibility to apply SFG to study ion channel protein gating mechanisms. The elucidation of peptide secondary structures at liquid crystal interfaces shows promising results that liqu...
Antimicrobial peptides, because of their unique structural and chemical properties, hold a promising future for the development of a new class of bacterial-resistant antibiotics, effective antimicrobial coatings, and high performance biosensors. To understand the structure/function relationship of surface-bound peptides as they relate to such applications, sum frequency generation (SFG) vibrational spectroscopy, coarse grained molecular dynamics simulations, and antimicrobial activity tests were used to characterize both surface peptide structural information and peptide activity. Results from MSI-78, an antimicrobial peptide, chemically immobilized via the N-(nMSI-78) or C-terminus (MSI-78n), demonstrate that the attachment site influences the structure and behavior of surface-bound peptides. Although both immobilized peptides adopt an α-helical structure in aqueous buffer, nMSI-78 stands up and MSI-78n lies down on the surface, as indicated by both SFG and MD simulations. Antimicrobial activity tests indicated that peptides that stand up interact with bacterial cells much quicker than peptides that lie down. We believe that this study provides fundamental insights into how to rationally engineer peptides and substrate surfaces to produce optimized abiotic/biotic interfaces for antimicrobial applications and beyond.
Interfacial water structure on a polymer surface in water (or surface hydration) is related to the antifouling activity of the polymer. Zwitterionic polymer materials exhibit excellent antifouling activity due to their strong surface hydration. It was proposed to replace zwitterionic polymers using mixed charged polymers because it is much easier to prepare mixed charged polymer samples with much lower costs. In this study, using sum frequency generation (SFG) vibrational spectroscopy, we investigated interfacial water structures on mixed charged polymer surfaces in water and how such structures change while being exposed to salt solutions and protein solutions. The 1:1 mixed charged polymer exhibits excellent antifouling property whereas other mixed charged polymers with different ratios of the positive/negative charges do not. It was found that on the 1:1 mixed charged polymer surface, SFG water signal is dominated by the contribution of the strongly hydrogen bonded water molecules, indicating strong hydration of the polymer surface. The responses of the 1:1 mixed charged polymer surface to salt solutions are similar to those of zwitterionic polymers. Interestingly, exposure to high concentrations of salt solutions leads to stronger hydration of the 1:1 mixed charged polymer surface after replacing the salt solution with water. Protein molecules do not substantially perturb the interfacial water structure on the 1:1 mixed charged polymer surface and do not adsorb to the surface, showing that this mixed charged polymer is an excellent antifouling material.
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