There has been an upsurge of green reductants for the preparation of graphene materials taking consideration of human health and the environment in recent years. In this paper, reduced graphene oxides (RGOs) were prepared by chemical reduction of graphene oxide (GO) with three green reductants, L-ascorbic acid (L-AA), D-glucose (D-GLC) and tea polyphenol (TP), and comparatively characterized by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectra, Raman spectra and electrical conductivity analysis. Results showed that all these three reductants were effective to remove oxygen-containing functional groups in GO and restore the electrical conductivity of the obtained RGO. The RGO sample with L-ascorbic acid as a reductant and reduced with the existence of ammonia had the highest electrical conductivity (9.8 S·cm-1) among all the obtained RGO samples. The mechanisms regarding to the reduction of GO and the dispersion of RGO in water were also proposed. It is the good dispersibility of reduced graphene oxide in water that will facilitate its further use in composite materials and conductive ink.

Multiwalled carbon nanotubes (MWCNTs) were used to convert radome materials to microwave absorbing materials. Dense MWCNT-fused silica composites were prepared by hot-pressing technique. The composites exhibit high complex permittivities at X-band frequencies, depending on the content of MWCNTs. The value of the loss tangent increases three orders over pure fused silica only by incorporating 2.5vol% MWCNTs into the composites. The average magnitude of microwave transmission reaches −33dB at 11–12GHz in the 10vol% MWCNT-fused silica composites, which indicates the composites have excellent microwave attenuation properties. The attenuation properties mainly originate from the electric loss of MWCNTs by the motion of conducting electrons.

Generally, photoanode-based photoelectrochemical immunoassay possesses obvious photocurrent response and lower detection limit for ideal sample detection, but it has the inherent imperfection of poor anti-interference capability for real sample detection. Photocathode-based immunoassay can well avoid the intrinsic drawback of photoanode-based immunoassay, but it has low photocurrent response resulting in less good sensitivity. Herein, a promising new cathode photoelectrochemical immunosensing platform integrating photocathode with photoanode was reported for accurate and sensitive detection of biomarkers. In this proposal, prostate-specific antigen (PSA, Ag) was chosen as a model of target analyte to exhibit the analytical performances of this platform. TiO/CdS:Mn hybrid structure modified indium-tin oxide (ITO) electrode served as photoanode, whereas CuInS microflowers modified ITO electrode was selected as photocathode. The transducer elements of PSA antibody (Ab) were modified on photocathode to fabricate a label-free cathode immunosensing electrode. The proposed immunosensing platform possesses two distinct advantages simultaneously. First, it has good anti-interference capability for the detection of real biological samples, since the biorecognition events occurred on photocathode. Second, the photoelectrochemical system owns evident photocurrent response and low detection limit for target Ag detection thanks to the introduction of the photoanode. Moreover, the proposed immunosensing platform also exhibits good specificity, reproducibility, and stability, and meanwhile it opens up a new horizon to construct other kinds of photoelectrochemical biosensors.

New tools for single‐cell interrogation enable deeper understanding of cellular heterogeneity and associated cellular behaviors and functions. Information of RNA expression in single cell could contribute to our knowledge of the genetic regulatory circuits and molecular mechanism of disease development. Although significant progresses have been made for intracellular RNA analysis, existing methods have a trade‐off between operational complexity and practical feasibility. We address this challenge by combining the ionic current rectification property of nanopipette reactor with duplex‐specific nuclease‐assisted hybridization chain reaction for signal amplification to realize a simple and practical intracellular nanosensor with minimal invasiveness, which enables single‐cell collection and electrochemical detection of intracellular RNA with cell‐context preservation. Systematic studies on differentiation of oncogenic miR‐10b expression levels in non‐malignant breast cells, metastatic breast cancer cells as well as non‐metastatic breast cancer cells were then realized by this nanotool accompanied by assessment of different drugs effects. This work has unveiled the ability of electrochemistry to probe intracellular RNA and opened new opportunities to study the gene expression and heterogeneous complexity under physiological conditions down to single‐cell level.

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The exploitation of singlet fission (SF) in photovoltaic devices is restricted by the limited number of SF materials available and the conflicting requirement of intermolecular interactions to satisfy both efficient SF and subsequent triplet extraction. Intramolecular SF (iSF) represents an emerging alternative, and may prove simpler to implement in devices. On account of the excellent chemical structure tunability and solution processability, conjugated polymers have emerged as promising candidates for iSF materials despite being largely underexplored. It remains a significant challenge to develop SF-capable conjugated polymers and achieve efficient dissociation of the formed triplet pairs simultaneously. In this contribution, we present a new iSF material in a para-azaquinodimethane-based quinoidal conjugated polymer. Using transient optical techniques, we show that an ultrafast iSF process dominates the deactivation of excited state in such polymer, featuring ultrafast population (< 1 ps) and stepwise dissociation of triplet pairs. Notably, these multiexciton states could further diffuse apart to produce long-lived free triplets (tens of μs) in strongly coupled aggregates in solid thin film. Such findings not only introduce a new iSF-active conjugated polymer to the rare SF material family, but also shed unique insight into interchain interaction-promoted triplet pair dissociation in aggregates of conjugated polymers, thus open new avenues for developing next-generation SF-based photovoltaic materials.

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Pyrite is the most common authigenic mineral preserved in many ancient sedimentary rocks. Pyrite also widely exists in the Longmaxi and Wufeng marine shales in the middle Yangtze area in South China. The Longmaxi and Wufeng shales were mainly discovered with 3 types of pyrites: pyrite framboids, euhedral pyrites and infilled framboids. Euhedral pyrites (Py4) and infilled framboids (Py5) belong to the diagenetic pyrites. Based on the formation mechanism of pyrites, the pyrites could be divided into syngenetic pyrites, early diagenetic pyrites, and late diagenetic pyrites. Under a scanning electron microscope (SEM), the syngenetic pyrites are mostly small framboids composed of small microcrystals, but the diagenetic pyrites are variable in shapes and the diagenetic framboids are variable in sizes with large microcrystals. Due to the deep burial stage, the pore space in the sediment was sharply reduced and the diameter of the late diagenetic framboids that formed in the pore space is similar to the diameter of the syngenetic framboids. However, the diameter of the syngenetic framboid microcrystals is suggested to range mainly from 0.3 µm to 0.4 µm, and that of the diagenetic framboid microcrystals is larger than 0.4 µm in the study area. According to the diameter of the pyrite framboids (D) and the diameter of the framboid microcrystals (d), the pyrite framboids could be divided into 3 sizes: syngenetic framboids (Py1, D < 5 µm, d ≤ 0.4 µm), early diagenetic framboids (Py2, D > 5 µm, d > 0.4 µm) and late diagenetic framboids (Py3, D < 5 µm, d > 0.4 µm). Additionally, the mean size and standard deviation/skewness values of the populations of pyrite framboids were used to distinguish the paleoredox conditions during the sedimentary stage. In the study area, most of the pyrite framboids are smaller than 5 µm, indicating the sedimentary water body was a euxinic environment. However, pyrite framboids larger than 5 µm in the shales indicated that the sedimentary water body transformed to an oxic-dysoxic environment with relatively low total organic carbon (TOC: 0.4–0.99%). Furthermore, the size of the framboid microcrystals could be used to estimate the gas content due to thermochemical sulfate reduction (TSR). The process of TSR occurs with oxidation of organic matter (OM) and depletes the H bond of the OM, which will influence the amount of alkane gas produced from the organic matter during the thermal evolution. Thus, syngenetic pyrites (d ranges from 0.35 µm to 0.37 µm) occupy the main proportion of pyrites in the Wufeng shales with high gas content (1.30–2.30 m3/t), but the Longmaxi shales (d ranges from 0.35 µm to 0.72 µm) with a relatively low gas content (0.07–0.93 m3/t) contain diagenetic pyrites. Because of TSR, the increasing size of the microcrystals may result in an increase in the value of δ13C1 and a decrease in the value of δ13C1-δ13C2. Consequently, the size of pyrite framboids and microcrystals could be widely used for rapid evaluation of the paleoredox conditions and the gas content in shales.