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Ningyan Cheng

Publications and source records attributed to Ningyan Cheng.

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Influence of Ru content on electrocatalytic activity and defect formation of Au-Pd-Pt-Ru compositionally complex solid solution thin films

Compositionally complex solid solutions (CCSSs) consist of a randomly mixed single phase with the potential to enhance electrocatalytic activity through their polyelemental surface atom arrangements. However, microstructural complexity originating from multiple principal elements influences local structure, chemistry, and lattice strain, which might also affect electrocatalytic activity. Here, we investigate the effect of Ru content on electrochemistry and defect formation in Au-Pd-Pt-Ru CCSS thin films. Such defects could provide active sites when terminating at the CCSS surface or modify surface composition through preferential segregation. A thin-film material library covering a wide composition range was fabricated by room-temperature combinatorial co-sputtering. High-throughput compositional, structural and functional characterization, including electron microscopy equipped with energy dispersive X-ray spectroscopy, X-ray diffraction, and electrochemical screening, were used to correlate composition and microstructural features with catalytic activity. Three representative compositions selected from the library - Au68Pd13Pt15Ru4, Au27Pd24Pt23Ru26, and Au9Pd21Pt18Ru52 - were examined in detail. The three samples exhibit face-centered cubic structures, with lattice contraction occurring with increasing Ru content. In addition, with increasing Ru content, a transition from a high density of nanotwins to high-density, atomic-layer stacking faults was observed. Moreover, the hydrogen evolution reaction activity improves with higher Ru content. Atom probe tomography reveals local compositional fluctuations, including element-specific enrichment and depletion at grain boundaries. The findings provide a new insight into surface atom arrangement design in the CCSS electrocatalysts with enhanced performance.

cond-mat.mtrl-sci

Coalescence of multiple topological orders in quasi-one-dimensional bismuth halide chains

Topology is being widely adopted to understand and to categorize quantum matter in modern physics. The nexus of topology orders, which engenders distinct quantum phases with benefits to both fundamental research and practical applications for future quantum devices, can be driven by topological phase transition through modulating intrinsic or extrinsic ordering parameters. The conjoined topology, however, is still elusive in experiments due to the lack of suitable material platforms. Here we use scanning tunneling microscopy, angle-resolved photoemission spectroscopy, and theoretical calculations to investigate the doping-driven band structure evolution of a quasi-one-dimensional material system, bismuth halide, which contains rare multiple band inversions in two time-reversal-invariant momenta. According to the unique bulk-boundary correspondence in topological matter, we unveil a composite topological phase, the coexistence of a strong topological phase and a high-order topological phase, evoked by the band inversion associated with topological phase transition in this system. Moreover, we reveal multiple-stage topological phase transitions by varying the halide element ratio: from high-order topology to weak topology, the unusual dual topology, and trivial/weak topology subsequently. Our results not only realize an ideal material platform with composite topology, but also provide an insightful pathway to establish abundant topological phases in the framework of band inversion theory.

cond-mat.mtrl-sci

Controllable and Continuous Quantum Phase Transitions in Intrinsic Magnetic Topological Insulator

The intrinsic magnetic topological material MnBi2Te4 has demonstrated great potential to investigate the interplay between topology and magnetism, which opens up new avenues for manipulating non-trivial electronic states and designing quantum devices. However, challenges and controversies remain due to its inevitable n-type antisite defects, hindering the experimental realization of intrinsic magnetic topological phenomena and rendering the precise control of topological phase transitions (TPTs) unachievable. Here, we study a candidate material family, Mn(1-x)GexBi2Te4, in which the heavy n-type doping features are strongly suppressed when the Ge content reaches 0.46, and multiple topological phases are well maintained with the surface Dirac point located near the Fermi level. Based on angle-resolved photoemission spectroscopy, transport measurements, and first-principles calculations, we reveal two magnetism-induced TPTs: the first is antiferromagnetic-ordering-induced transition from strong topological insulator to a magnetic topological insulator as revealed by gap opening of topological surface states; the second is external-magnetic-field-dependent transition from magnetic topological insulator to a Weyl semimetal with the gap reclosed. Our work paves the way for the realization of intrinsic magnetic topological states in MnBi2Te4 family and provides an ideal platform for achieving controllable and continuous TPTs towards future spintronic applications.

cond-mat.mtrl-sci

Mass Acquisition of Dirac Fermions in Bi4I4 by Spontaneous Symmetry Breaking

Massive Dirac fermions, which are essential for realizing novel topological phenomena, are expected to be generated from massless Dirac fermions by breaking the related symmetry, such as time-reversal symmetry (TRS) in topological insulators or crystal symmetry in topological crystalline insulators. Here, we report scanning tunneling microscopy and angle-resolved photoemission spectroscopy studies of {\alpha}-Bi4I4, which reveals the realization of massive Dirac fermions in the (100) surface states without breaking the TRS. Combined with first-principle calculations, our experimental results indicate that the spontaneous symmetry breaking engenders two nondegenerate edges states at the opposite sides of monolayer Bi4I4 after the structural phase transition, imparting mass to the Dirac fermions after taking the interlayer coupling into account. Our results not only demonstrate the formation of the massive Dirac fermions by spontaneous symmetry breaking, but also imply the potential for the engineering of Dirac fermions for device applications.

cond-mat.mtrl-sci

Towards Layer-Selective Quantum Spin Hall Channels in Weak Topological Insulator Bi4Br2I2

Weak topological insulators, constructed by stacking quantum spin Hall insulators with weak interlayer coupling, offer promising quantum electronic applications through topologically nontrivial edge channels. However, the currently available weak topological insulators are stacks of the same quantum spin Hall layer with translational symmetry in the out-of-plane direction, leading to the absence of the channel degree of freedom for edge states. Here, we study a candidate weak topological insulator, Bi4Br2I2, which is alternately stacked by three different quantum spin Hall insulators, each with tunable topologically non-trivial edge states. Our angle-resolved photoemission spectroscopy and first-principles calculations show that an energy gap opens at the crossing points of different Dirac cones correlated with different layers due to the interlayer interaction. This is essential to achieve the tunability of topological edge states as controlled by varying the chemical potential. Our work offers a perspective for the construction of tunable quantized conductance devices for future spintronic applications.

cond-mat.mtrl-sci

Two-dimensional ZIF-L nanosheets as high performance non-enzymatic glucose sensor

An effective biosensor based on two-dimensional (2D) Co-ZIF-L nanosheets for sensitive electrochemical non-enzymatic glucose detection is developed, which exhibits high electrocalalytic activities towards glucose due to the ordered porous structure as well as ultrahigh specific surface area. The fabricated Co-ZIF-L nanosheets electrodes present an outstanding performance with higher sensitivity of 769.5 *10$^{-6}$ A mM$^{-1}$ cm$^{-2}$ and lower detect limit of 90.4 nM, while the constructed 3D ZIF-67 nanoparticles electrodes show a weaker sensitivity of 697.4 *10$^{-6}$ A mM$^{-1}$ cm$^{-2}$ and a limited detection range from 2 *10$^{-6}$ M to 414 *10$^{-6}$ M. Furthermore, the Co-ZIF-L based non-enzymatic glucose biosensors possess an acceptable selectivity, long-term stability as well as reproducibility. This work may offer a new approach to develop 2D ZIF nanosheets as a potential candidate in electrochemical biosensors.

physics.app-ph