A branched ZnO-CdS double-shell NW array on the surface of a carbon fiber (CF/ZnO-CdS) was successfully synthesized via a facile two-step hydrothermal method. Based on a single CF/ZnO-CdS wire on a polymer substrate, a flexible photodetector was fabricated, which exhibited ultrahigh photon responsivity under illuminations of blue light (1.11 × 10(5) A/W, 8.99 × 10(-8) W/cm(2), 480 nm), green light (3.83 × 10(4) A/W, 4.48 × 10(-8) W/cm(2), 548 nm), and UV light (1.94 × 10(5) A/W, 1.59 × 10(-8) W/cm(2), 372 nm), respectively. The responsivity of this broadband photon sensor was enhanced further by as much as 60% when the device was subjected to a -0.38% compressive strain. This is because the strain induced a piezopotential in ZnO, which tunes the barrier height at the ZnO-CdS heterojunction interface, leading to an optimized optoelectronic performance. This work demonstrates a promising application of piezo-phototronic effect in nanoheterojunction array based photon detectors.

Using fluorescently labeled DNA oligonucleotides and nanomaterials for developing biosensors has been extensively reported for gold nanoparticles (AuNPs) and graphene oxide (GO) among others. These materials have vastly different affinities and mechanisms for interacting with DNA, and their analytical performance is likely to be different. In this work, we used several DNA sequences and, respectively, adsorbed them on AuNPs and GO to quench fluorescence. Different from previous work, we used KCN to fully dissolve the AuNPs to calculate the percentage of the desorbed DNA due to the complementary DNA (cDNA) and aptamer target. The desorbed probe DNA from the AuNPs was less than 5% for all of the targets including DNA, adenosine, Hg2+, and lysozyme, indicating a very strong DNA adsorption affinity. Desorption of DNA was achieved by adding HEPES buffer, NaCl, and As­(III), but such desorption was attributed to the adsorption of these molecules or ions by the AuNPs instead of their interaction with the adsorbed DNA. For GO, more probes desorbed with addition of target analytes but so did nonspecific desorption by random DNA and proteins. In summary, AuNPs are unlikely to be a good surface for developing biosensors relying solely on the desorption of probe DNA, while for GO the main problem is nonspecific desorption.

No abstract

On-site monitoring the plantation of genetically modified (GM) crops is of critical importance in agriculture industry throughout the world. In this paper, a simple, visual and instrument-free method for instant on-site detection of GTS 40-3-2 soybean has been developed. It is based on body-heat recombinase polymerase amplification (RPA) and followed with naked-eye detection via fluorescent DNA dye. Combining with extremely simplified sample preparation, the whole detection process can be accomplished within 10 min and the fluorescent results can be photographed by an accompanied smart phone. Results demonstrated a 100% detection rate for screening of practical GTS 40-3-2 soybean samples by 20 volunteers under different ambient temperatures. This method is not only suitable for on-site detection of GM crops but also demonstrates great potential to be applied in other fields.

The CRISPR/Cas12a (cpf1) system was reported to indiscriminately cleave single-stranded DNA after binding with target DNA strands. This usually required the target DNA strands to contain the protospacer-adjacent motif (PAM) sequence of TTTN. Herein, we found Cas12a can also recognize another PAM sequence of UUUN resulting in activation of its ssDNA collateral cleavage effect. To make this finding useful, by combining with LAMP, we first realized CRISPR/Cas12a for directly visualized DNA detection at the single-copy level. By treating with UDG enzyme, we made this system free from residual amplicon contamination, which is a big problem in this field. Thus, an ultrasensitive and anticontaminant DNA detection platform, namely, UDG and LAMP and CRISPR (ULC). This new finding would help us better understand the mechanism of Cas12a and expand its application.

The synthesis scheme for the formation pathway of monometallic and bimetallic nanoparticles supported on hydrochar derived from lignin-rich precursory biomass.

No abstract

Pursuit of a simple, fast, and cost-effective method to prepare highly and dual-wavelength fluorescent carbon quantum dots (CQDs) is a persistent objective in recent years. Here, we fabricated N-doped micropore carbon quantum dots (NM-CQDs) with a high quantum yield and dual-wavelength photoluminescence (PL) emission from sustainable biomass using a pulsed laser ablation method. Interestingly, two coexisting indigo–blue photoluminescence (PL) emissions were clearly observed, elucidating that the excited electrons transited from the intrinsic π* orbital to the surface state (SS) formed from the saturation passivation. The quantum yield (QY) and fluorescence lifetime (FL) of the obtained NM-CQDs were as high as 32.4% and 6.56 ns. Further investigations indicated that the emission behaviors of NM-CQDs were still stable and independent in various conditions such as various excitation wavelengths, salt ionic concentrations, pH values, irradiation times, and temperatures. The obtained NM-CQDs are very suitable for cellular staining images due to strong and stable PL emission and show good internalization in different cells. Therefore, we propose a new and cost-effective preparation strategy for highly fluorescent NM-CQDs with great potential in biomedical imaging and engineering.