Spectroscopic Studies of Quasiparticle Low-Energy Excitations in Cuprate and Iron-Based High-Temperature Superconductors

Recent development in the physics of high-temperature superconductivity (SC) is reviewed, with special emphasis on the studies of the low-energy excitations of cuprate and iron-based superconductors. For cuprate superconductors, a phenomenology based on coexisting competing orders with superconductivity in the ground state of these doped Mott insulators is shown to provide a consistent account for a wide range of experimental findings. In the case of iron-based superconductors, studies of the low-energy excitations reveal interesting similarities and differences when compared with cuprate superconductors. In contrast to the single-band cuprate superconductivity with an insulating parent state, the ferrous superconductors are multi-band materials with a semi-metallic parent state and exhibit two-gap superconductivity when doped. On the other hand, both systems exhibit strong antiferromagnetic correlation and Fermi-surface distortion, leading to unconventional pairing symmetries with sign-changing order parameters on different parts of the Fermi surface. These findings suggest that the pairing potentials in both the cuprate and the ferrous superconductors are generally repulsive, thus favoring a pairing mechanism that is electronically driven and a pairing strength that is closely related to the electronic correlation. The physical implications of the unified phenomenology based on antiferromagnetic correlations and remaining open issues associated with the cuprate and ferrous superconductivity are discussed

Fractionalized quantum excitations in correlated two-dimensional topological phases

The research field of topological phases and materials is one of the most exciting frontiers in modern condensed matter physics [1]; [2]; [3]; [4]; [5]; [6] ; [7]. In contrast to the classification of conventional condensed matter phases according to their symmetries, different topological states of matter generally do not involve broken symmetries. Rather, they are associated with certain fundamental physical properties that are insensitive to smooth changes in materials parameters. Therefore, a topological state cannot change into another unless the system undergoes a quantum phase transition [6] ; [7]

Mildred S. Dresselhaus (1930–2017): A fierce force of harmony

Prof. Mildred S. Dresselhaus, fondly known as “Millie” and “Queen of Carbon Science,” passed away at age 86 on February 20, 2017. She was a pioneer in the research of carbon nanomaterials, a giant in experimental condensed matter physics, a fine musician, a compassionate mentor and role model to young people, a strong advocate for women in science and engineering, and a selfless and impactful citizen of the scientific community

Single-step growth of graphene and graphene-based nanostructures by plasma-enhanced chemical vapour deposition

The realization of many promising technological applications of graphene and graphene-based nanostructures depends on the availability of reliable, scalable, high-yield and low-cost synthesis methods. Plasma enhanced chemical vapor deposition (PECVD) has been a versatile technique for synthesizing many carbon-based materials, because PECVD provides a rich chemical environment, including a mixture of radicals, molecules and ions from hydrocarbon precursors, which enables graphene growth on a variety of material surfaces at lower temperatures and faster growth than typical thermal chemical vapor deposition. Here we review recent advances in the PECVD techniques for synthesis of various graphene and graphene-based nanostructures, including horizontal growth of monolayer and multilayer graphene sheets, vertical growth of graphene nanostructures such as graphene nanostripes with large aspect ratios, direct and selective deposition of monolayer and multi-layer graphene on nanostructured substrates, and growth of multi-wall carbon nanotubes. By properly controlling the gas environment of the plasma, it is found that no active heating is necessary for the PECVD growth processes, and that high-yield growth can take place in a single step on a variety of surfaces, including metallic, semiconducting and insulating materials. Phenomenological understanding of the growth mechanisms are described. Finally, challenges and promising outlook for further development in the PECVD techniques for graphene-based applications are discussed

Selective formation of pyridinic-type nitrogen-doped graphene and its application in lithium-ion battery anodes

We report a high-yield single-step method for synthesizing nitrogen-doped graphene nanostripes (N-GNSPs) with an unprecedentedly high percentage of pyridinic-type doping (>86% of the nitrogen sites), and investigate the performance of the resulting N-GNSPs as a lithium-ion battery (LIB) anode material. The as-grown N-GNSPs are compared with undoped GNSPs using scanning electron microscopy (SEM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), helium ion-beam microscopy (HIM), and electrochemical methods. As an anode material we find that pyridinic-type N-GNSPs perform similarly to undoped GNSPs, suggesting that pyridinic sites alone are not responsible for the enhanced performance of nitrogen-doped graphene observed in previous studies, which contradicts common conjectures. In addition, post-mortem XPS measurements of nitrogen-doped graphene cycled as a lithium-ion battery anode are conducted for the first time, which reveal direct evidence for irreversible chemical changes at the nitrogen sites during cycling. These findings therefore provide new insights into the mechanistic models of doped graphene as LIB anodes, which are important in improving the anode designs for better LIB performance

Vertically-aligned graphene nanowalls grown via plasma-enhanced chemical vapor deposition as a binder-free cathode in Li-O_2 batteries

In the present report, vertically-aligned graphene nanowalls are grown on Ni foam (VA-G/NF) using plasma-enhanced chemical vapor deposition method at room temperature. Optimization of the growth conditions provides graphene sheets with controlled defect sites. The unique architecture of the vertically-aligned graphene sheets allows sufficient space for the ionic movement within the sheets and hence enhancing the catalytic activity. Further modification with ruthenium nanoparticles (Ru NPs) drop-casted on VA-G/NF improves the charge overpotential for lithium–oxygen (Li–O_2) battery cycles. Such reduction we believe is due to the easier passage of ions between the perpendicularly standing graphene sheets thereby providing ionic channels

Single-step growth of graphene and graphene-based nanostructures by plasma-enhanced chemical vapour deposition

The realization of many promising technological applications of graphene and graphene-based nanostructures depends on the availability of reliable, scalable, high-yield and low-cost synthesis methods. Plasma enhanced chemical vapor deposition (PECVD) has been a versatile technique for synthesizing many carbon-based materials, because PECVD provides a rich chemical environment, including a mixture of radicals, molecules and ions from hydrocarbon precursors, which enables graphene growth on a variety of material surfaces at lower temperatures and faster growth than typical thermal chemical vapor deposition. Here we review recent advances in the PECVD techniques for synthesis of various graphene and graphene-based nanostructures, including horizontal growth of monolayer and multilayer graphene sheets, vertical growth of graphene nanostructures such as graphene nanostripes with large aspect ratios, direct and selective deposition of monolayer and multi-layer graphene on nanostructured substrates, and growth of multi-wall carbon nanotubes. By properly controlling the gas environment of the plasma, it is found that no active heating is necessary for the PECVD growth processes, and that high-yield growth can take place in a single step on a variety of surfaces, including metallic, semiconducting and insulating materials. Phenomenological understanding of the growth mechanisms are described. Finally, challenges and promising outlook for further development in the PECVD techniques for graphene-based applications are discussed

Vertically-aligned graphene nanowalls grown via plasma-enhanced chemical vapor deposition as a binder-free cathode in Li-O_2 batteries

In the present report, vertically-aligned graphene nanowalls are grown on Ni foam (VA-G/NF) using plasma-enhanced chemical vapor deposition method at room temperature. Optimization of the growth conditions provides graphene sheets with controlled defect sites. The unique architecture of the vertically-aligned graphene sheets allows sufficient space for the ionic movement within the sheets and hence enhancing the catalytic activity. Further modification with ruthenium nanoparticles (Ru NPs) drop-casted on VA-G/NF improves the charge overpotential for lithium–oxygen (Li–O_2) battery cycles. Such reduction we believe is due to the easier passage of ions between the perpendicularly standing graphene sheets thereby providing ionic channels