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Chirality separation of single-wall carbon nanotubes (SWCNTs) is key to enabling applications in single photon sources, optoelectronic devices and bioimaging, and it generally requires multiple separation steps to obtain single chirality species with the desired purity. In this work, we report the use of a novel sodium hyodeoxycholate (SHC) surfactant for separation of single-chirality SWCNTs. The results demonstrated that chirality-selective adsorption and desorption of SWCNTs on a gel column can be achieved readily by modulating the concentrations of the SHC-based mixed surfactants. Through an optimized one-step procedure, single-chirality (6,5) SWCNTs were successfully separated, and the chirality purity was estimated to be 97% by using a spectroscopic approach, exceeding most reported purities for traditional surfactant-based one- or multiple-step separations. Due to the ultrahigh chirality resolution of the present method, the (6,5) SWCNTs can also be effectively separated from different SWCNT materials with various diameter or chirality distributions, even from materials containing very few (6,5) SWCNTs. The high-purity chirality separation demonstrated in this work lays an important foundation for the industrial production and applications of single-chirality SWCNTs. [Display omitted] [ABSTRACT FROM AUTHOR]

Structural control of single-wall carbon nanotubes (SWCNTs) with uniform properties is critical not only for their property modulation and functional design but also for applications in electronics, optics, and optoelectronics. To achieve this goal, various separation techniques have been developed in the past 20 years through which separation of high-purity semiconducting/metallic SWCNTs, single-chirality species, and even their enantiomers have been achieved. This progress has promoted the property modulation of SWCNTs and the development of SWCNT-based optoelectronic devices. Here, the recent advances in the structure separation of SWCNTs are reviewed, from metallic/semiconducting SWCNTs, to single-chirality species, and to enantiomers by several typical separation techniques and the application of the corresponding sorted SWCNTs. Based on the separation procedure, efficiency, and scalability, as well as, the separable SWCNT species, purity, and quantity, the advantages and disadvantages of various separation techniques are compared. Combined with the requirements of SWCNT application, the challenges, prospects, and development direction of structure separation are further discussed. [ABSTRACT FROM AUTHOR]

The intersubband plasmons (ISBPs) of single‐wall carbon nanotubes (SWCNTs) endow SWCNT‐based optoelectronic devices with more functions. However, the structural dependence of the ISBPs of SWCNTs is not fully understood. Here, the effect of electronic types and diameters of SWCNTs on the energy and intensity of their ISBPs is investigated systematically. The results show that the ISBP energy of semiconducting SWCNTs is ≈50–250 meV larger than that of metallic SWCNTs with the same diameters, while the ISBP integral intensity is approximately 1.25 to 4 times stronger. Diameter dependence of ISBPs for both semiconducting and metallic SWCNTs is also observed. With a decrease in diameter, the ISBPs shift to higher energies, while the intensity decreases dramatically. When the diameter is reduced to less than 1 nm, the ISBPs become unobservable. Interestingly, the energy separation between the ISBPs and interband transition S22 (M11) decreases with an increase in diameter. Theoretical calculations show that the structure‐dependent ISBP characteristics are dominated by the electronic states of SWCNTs. Based on the ISBP characteristics of different SWCNTs, high‐performance SWCNT‐based near‐infrared electrochromic devices are fabricated by mixing small‐diameter metallic SWCNTs with semiconducting SWCNTs due to their high conductivity and negligible ISBP signals. [ABSTRACT FROM AUTHOR]

There is strong demand for higher energy density and flexible lithium ion batteries recently. Unfortunately, electrodes built by conventional methods cannot meet these requirements simultaneously due to the large amount of inactive additives needed for sufficient flexibility. Herein, by utilizing a continuous single‐walled carbon nanotube reticulation and designing an all‐in‐one hierarchical configuration, binder‐free electrodes are fabricated via an in situ integration procedure. The electrode exhibits excellent electrochemical performance against up to 20 000 cycles of bending and high energy density (up to 493 Wh kg−1electrode and 820 Wh L−1electrode). The hierarchical configuration takes full diverse advantages of different carbon nanostructures. The as‐obtained novel binder‐free electrodes exhibit not only good cyclability (up to ≈90% capacity retentions after 1500 cycles) with only 4 wt% additive materials, but also show enhanced kinetic process, in comparison to those of traditional electrodes. Furthermore, based on the as‐designed electrodes, flexible cells are assembled and a practical wearable system is fabricated, manifesting that they can be used in a stable and flexible power supply for smart systems. [ABSTRACT FROM AUTHOR]