Phase interrogation SPR sensing based on white light polarized interference for wide dynamic detection range

A phase surface plasmon resonance (SPR) sensing technology based on white light polarized interference in common-path geometry is reported. A halogen lamp is used as the excitation source of the SPR sensor. The fixed optical path difference (OPD) between p- and s-polarized light is introduced by a birefringence crystal to produce sinusoidal spectral interference fringes. The SPR phase is accurately extracted from the interference fringes using a novel iterative parameter-scanning cross-correlation algorithm. The dynamic detection range is expanded by tracking the best SPR wavelength, which is identified using a window Fourier algorithm. The experimental results show that the sensitivity of this SPR system was 1.3 × 10−7 RIU, and the dynamic detection range was 0.029 RIU. This sensor, not only simple to implement and cost efficient, requires no modulators

Degradable mesoporous semimetal antimony nanospheres for near-infrared II multimodal theranostics.

Metallic and semimetallic mesoporous frameworks are of great importance owing to their unique properties and broad applications. However, semimetallic mesoporous structures cannot be obtained by the traditional template-mediated strategies due to the inevitable hydrolytic reaction of semimetal compounds. Therefore, it is yet challenging to fabricate mesoporous semimetal nanostructures, not even mention controlling their pore sizes. Here we develop a facile and robust selective etching route to synthesize monodispersed mesoporous antimony nanospheres (MSbNSs). The pore sizes of MSbNSs are tunable by carefully controlling the partial oxidation of Sb nuclei and the selective etching of the as-formed Sb2O3. MSbNSs show a wide absorption from visible to second near-infrared (NIR-II) region. Moreover, PEGylated MSbNSs are degradable and the degradation mechanism is further explained. The NIR-II photothermal performance of MSbNSs is promising with a high photothermal conversion efficiency of ~44% and intensive NIR-II photoacoustic signal. MSbNSs show potential as multifunctional nanomedicines for NIR-II photoacoustic imaging guided synergistic photothermal/chemo therapy in vivo. Our selective etching process would contribute to the development of various semimetallic mesoporous structures and efficient multimodal nanoplatforms for theranostics

Efficient Selective Sorting of Semiconducting Carbon Nanotubes Using Ultra-Narrow-Band-Gap Polymers

[Image: see text] Conjugated polymers with narrow band gaps are particularly useful for sorting and discriminating semiconducting single-walled carbon nanotubes (s-SWCNT) due to the low charge carrier injection barrier for transport. In this paper, we report two newly synthesized narrow-band-gap conjugated polymers (PNDITEG-TVT and PNDIC8TEG-TVT) based on naphthalene diimide (NDI) and thienylennevinylene (TVT) building blocks, decorated with different polar side chains that can be used for dispersing and discriminating s-SWCNT. Compared with the mid-band-gap conjugated polymer PNDITEG-AH, which is composed of naphthalene diimide (NDI) and head-to-head bithiophene building blocks, the addition of a vinylene linker eliminates the steric congestion present in head-to-head bithiophene, which promotes backbone planarity, extending the π-conjugation length and narrowing the band gap. Cyclic voltammetry (CV) and density functional theory (DFT) calculations suggest that inserting a vinylene group in a head-to-head bithiophene efficiently lifts the highest occupied molecular orbital (HOMO) level (−5.60 eV for PNDITEG-AH, −5.02 eV for PNDITEG-TVT, and −5.09 eV for PNDIC8TEG-TVT). All three polymers are able to select for s-SWCNT, as evidenced by the sharp transitions in the absorption spectra. Field-effect transistors (FETs) fabricated with the polymer:SWCNT inks display p-dominant properties, with higher hole mobilities when using the NDI-TVT polymers as compared with PNDITEG-AH (0.6 cm(2) V(–1) s(–1) for HiPCO:PNDITEG-AH, 1.5 cm(2) V(–1) s(–1) for HiPCO:PNDITEG-TVT, and 2.3 cm(2) V(–1) s(–1) for HiPCO:PNDIC8TEG-TVT). This improvement is due to the better alignment of the HOMO level of PNDITEG-TVT and PNDIC8TEG-TVT with that of the dominant SWCNT specie

High-throughput imaging surface plasmon resonance biosensing based on ultrafast two-point spectral-dip tracking scheme

Wavelength interrogation surface plasmon resonance imaging (λSPRi) has potential in detecting 2-dimensional (2D) sensor array sites, but the resonance wavelength imaging rate limits the application of detecting biomolecular binding process in real time. In this paper, we have successfully demonstrated an ultrafast λSPRi biosensor system. The key feature is a two-point tracking algorithm that drives the liquid crystal tunable filter (LCTF) to achieve fast-tracking of the resonance wavelength movement caused by the binding of target molecules with the probe molecules on the sensing surface. The resonance wavelength measurement time is within 0.25s. To date, this is the fastest speed ever reported in λSPRi. Experiment results show that the sensitivity and dynamic are 2.4 × 10−6 RIU and 4.6 × 10−2 RIU, respectively. In addition, we have also demonstrated that the system has the capability of performing fast high-throughput detection of biomolecular interactions, which confirms that this fast real-time detecting approach is most suitable for high-throughput and label-free biosensing applications

Polar Side Chains Enhance Selection of Semiconducting Single-Walled Carbon Nanotubes by Polymer Wrapping

This paper describes the effectiveness of donor-acceptor (D-A) conjugated polymers to disperse and select for semiconducting single-walled carbon nanotubes (s-SWCNTs) when enhanced by the inclusion of polar oligoethylene glycol-based side chains, without altering the D-A backbone. We designed and synthesized two sets of naphthalenediimide(NDI)-alt-bithiophene(T2)-based conjugated polymers with one of two alkyl side chains (decyl and dodecyl chains) of different lengths and with or without polar triethylene glycol side chains. The resulting low-band-gap copolymers all effectively disperse and select for s-SWCNT, but the inclusion of polar side chains enhances the interactions between the polymer backbone and the walls of the s-SWCNTs relative to the polymers with only alkyl side chains. As a result, the wrapping and selection efficiency of the polymer-SWCNT systems with polar side chains are both significantly enhanced. We further optimized the binding energy and surface coverage by combining glycol ether and dodecyl side chains to maximize wrapping efficiency, leading to a field-effect mobility of 2.82 cm2 V-1 s-1 and on/off current ratios of ∼2 × 107 in polymer-wrapped SWCNTs. Our results provide insight into the role of the side-chain interactions in the polymer wrapping and dispersion technique, and, because we focus on manipulating side chains, they can be generalized for other conjugated polymer backbones