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In a new era of booming information technology, E-commerce has become an important developing country in China, and parents and students have gradually welcomed this profession. In the information age, how to improve the quality of training in professional higher education and then meet the employment needs of industries and enterprises has become a key issue for higher vocational education in China. This article mainly studies the E-commerce professional talent training model based on identity inheritance. This article analyzes the current situation of E-commerce talent training, combines pragmatism, and proposes strategies for training talented E-commerce experts in underdeveloped western regions. The theory of business talent development has certain theoretical significance for guiding and promoting electronic trade and socioeconomic development. The research in this article shows that despite a large number of international trade graduates every year, the electronic trading group (70.1%) is still international trade, and 85.9% of companies still believe that there is a gap between transnational E-commerce traders. In order to “effectively connect” the training of E-commerce talents in higher vocational education and social needs, it is necessary to take the needs of industrial development as the driving force and market demand as the guidance and take practical measures to improve the school-enterprise matching. The distance between talents ultimately promotes professional construction and talent training and achieves a win-win situation for both schools and enterprises.

This work reports a microfluidic paper-based photoelectrochemical (μ-PEC) sensing platform for thrombin (TB) detection with electron-transfer tunneling distance regulation (ETTDR) and aptamer target-triggering nicking enzyme signaling amplification (NESA) dual strategies. Specifically, paper-based TiO2 nanosheets (PTNs) were prepared with an efficient hydrothermal process, serving as the direct pathway for the charge carriers transfer. When CeO2-labeled hairpin DNA 3 (HP3) was closely located at the PTNs, the CeO2-PTNs heterostructure was formed, which could great facilitate the photogenerated carries separation of CeO2. In addition, with the aid of aptamer target-triggering NESA strategy, the input TB could be transducted to numerous output target of DNA (tDNA), achieving the goal of desirable signal amplification. In the presence of TB, the output tDNA could be further hybridized with HP3 and unfold its hairpin loop, which forced the CeO2 away from the surface of PTNs and vanished the CeO2-PTNs heterostructure, resulting in the obviously reducing of photocurrent signal. The as-designed sensing platform exhibited a linear range from 0.02 pM to 100 pM with a detection limit of 6.7 fM. Importantly, this μ-PEC sensing platform could not only realize the highly efficient TB detection, but also pave a luciferous way for the detection of other protein in bioanalysis.

Exploring novel photoactive materials with high photoelectric conversion efficiency plays a crucial role in enhancing the analytical performance of paper-based photoelectrochemical (PEC) biosensor. SnO

Exploring efficient luminophores in the electrochemiluminescence (ECL) system is highly desired to pursue a sensitive ECL sensing platform. Herein, the black phosphorus nanosheets (BP NSs) with excellent ECL properties are investigated and serve as the luminophore with the coreactant of peroxydisulfate (S2O82-) solution. Moreover, owing to the overlapping of emission and absorbance spectra, effective resonance energy transfer (RET) is realized between the BP NSs and the introduced Au nanoparticles. In order to achieve the portable and miniaturized developing trends for the paper-based ECL sensing platform, a paper-based perovskite solar cell (PSC) device is designed to act as the power source to replace the commonly utilized expensive and cumbersome electrochemical workstation. Benefiting from that, a PSC driven paper-based constant potential ECL-RET sensing platform is constructed, thereby realizing sensitive microRNAs (miRNAs) detection. What's more, to attain the preferable analytical performance, the duplex-specific nuclease (DSN) is also introduced to assist the target recycling signal amplification strategy. Based on this, highly sensitive detection of miRNA-107 with a range from 0.1 pM to 15 nM is achieved by this designed sensing platform. Most importantly, this work not only pioneers a precedent for developing a high-sensitivity PSC triggered ECL sensing platform but also explores the application prospect of BP nanomaterial in the field of bioanalysis.

For typical planar perovskite solar cell, an electron transporting layer (ETL) plays an important role in extracting electrons from a perovskite layer and blocking electron-hole recombination at the perovskite/conductive substrate interface. To date, TiO 2 or ZnO ETLs are mainly adopted in both forms of film and nanostructure due to their ease of preparation. Nevertheless, the photoinstability of TiO 2 and thermal instability of ZnO/perovskite interface remain the major challenges limiting their potential commercialization. Herein, we demonstrate an effective in situ template self-etching ( i TSE) strategy to grow the novel hollow domed SnO 2 nanotubes array with ZnO nanorods as sacrifice templates and the growth mechanism of such SnO 2 nanotubes has been proposed based on a series of controllable experiments. Using such SnO 2 nanotube as ETL for perovskite solar cell demonstrates a high photocurrent density of 15.9 mA/cm 2 at a based-voltage of 760 mV, leading to a stable power conversion efficiency of 12.1% over 1000 s under the simulated AM 1.5G one sun illumination. This work highlights the importance of the ETL material selection and provides insights into achieving an ideal ETL/substrate homojunction to facilitate electron transporting.

This work described that one–step synthesis three dimensional anatase hierarchically cactus–like TiO 2 arrays (AHCT) and their application in constructing a novel photoelectrochemical (PEC) and visualized sensing platform based on molecular imprinting technique, which reports its result with the prussian blue (PB) electrode served as the electrochromic indicator for the detection of glycoprotein (RNase B). The AHCT arrays were perpendicularly grown on FTO substrate with tunable sizes, offering many advantages, such as large contact area, rapid charge electron separation and transport. A possible formation process of the interesting AHCT arrays has been investigated based on time–dependent experiment. In addition, the PEC and visualized sensing platform was constructed based on the molecularly imprinted polymer modified AHCT arrays. Specifically, in the proposed system, the more RNase B being, the more insulating layer was formed on the surface of AHCT arrays that impeded the harvesting of light and electron transfer, resulting in the reduction of photocurrent. When upon light illumination, the photogenerated electrons flow through an external circuit to PB, leading to the reduction of PB to prussian white (PW), which is transparent. The rate of decolourization of PB is proportional to the concentration of RNase B. In this way, a visualized PEC sensing platform that gives its quantitative information could be performed by monitoring the change of color intensity. Under optimal conditions, the protocol possessed a detection range of 0.5 pM to 2 μM (r=0.997) and the limit of detection was 0.12 pM toward RNase B. Our method eliminates the need for sophisticated instruments and high detection expenses, making it possible to be a reliable alternative in resource–constrained regions.

By incorporating the Prussian Blue (PB) electrochromic display as cathode, a solar-driven photoelectrochemical (PEC) cell was constructed through combining sandwich-structured graphite-like carbon nitride (g-C3N4)-Au-branched-titanium dioxide (B-TiO2) nanorods as photoanode for self-powered hydrogen peroxide (H2O2) sensing, which exhibits both direct photoelectrochemical and electrochromic response. The gold nanoparticles (Au NPs) sandwiched between the B-TiO2 nanorods and the g-C3N4 layer served as electron relay as well as plasmonic photosensitizer to enhance the solar-to-chemical energy conversion efficiency. Owing to the effective disproportionation of H2O2 and specific recognition of mannose on cell surface, concanavalin-A conjugated porous AuPd alloy nanoparticles were introduced as the catalytically active nanolabels promoting generation of hydroxyl radicals (·OH). Based on the cleavage of DNA with the participation of ·OH radicals generated by the decomposition of H2O2 under the catalysis of AuPd alloy result in the disassembly of cancer cells to achieve further signal enhancement. The multiple-signal-output sensing response not only provides a promising strategy for different analytical purposes based on novel stimuli-responsive materials, but also enhances the reliability in the analyte detection.

In this work, a novel sensing platform based on visible light driven biofuel cell (BFC) has been facilely designed for sensitive detection of prostate-specific antigen (PSA) with the photo-response bioanode, realizing the dual route energy conversion of light energy and chemical energy to electricity. The hierarchical branched TiO2 nanorods (B-TiO2 NRs) decorated with CdS quantum dots (QDs) act as the substrate to confine glucose dehydrogenase (GDH) for the visible light driven glucose oxidation at the bioanode. Three dimensional flowers like hierarchical carbon/gold nanoparticles/bilirubin oxidase (3D FCM/AuNPs/BOD) bioconjugate served as biocatalyst for O2 reduction at the biocathode. With an increase in the concentration of PSA, the amount of BOD labels on biocathode increases, thus leading to the higher current output of the as-proposed visible light driven BFC. Based on this, this sensing platform provide great performance in sensitivity and specificity, increasing linear detection range from 0.3pgmL(-1) to 7μgmL(-1) with a detection limit of 0.1pgmL(-1). Most importantly, our new sensing strategy provided a simple and inexpensive sensing platform for tumor markers detection, suggesting its wide potential applications for clinical diagnostics.

By controlling target-induced signal quencher release, a label-free and modification-free microfluidic paper based photoelectrochemical analytical device (μ-PAD) for cardiac troponin-I (cTnI) detection was designed for the first time. To achieve it, cellulose paper based single-crystalline three-dimensional aloe like TiO

In this work, an electrochemiluminescence (ECL) immunoassay integrated with the proposed 3D microfluidic origami device for the sensitive detection of carcinoembryonic antigen (CEA) was developed based on Ag nanospheres modified paper working electrode (Ag-PWE) as the sensor platform and Au nanocages functionalized tris-(bipyridine)-ruthenium(II) (Ru(bpy)32+) as the ECL signal amplification label. The novel Ag-PWE with excellent conductivity was constructed through the growth of an Ag nanosphere layer on the surfaces of cellulose fibers and served to provide a good pathway for electron transfer and enhance the amount of captured antibody (Ab1). Au nanocages, which possessed a hollow structure, were first used to construct the ECL immunosensor as a signal amplification carrier. Both the inner and outer surfaces of the Au nanocages can adsorb Ru(bpy)32+, therefore the signal can be amplified as much as possible. In addition, this as-prepared 3D microfluidic origami ECL immunodevice had the advantages of high sensitivity, acceptable precision and reasonable accuracy. On the basis of the considerably amplified ECL signal and sandwich-type format, the as-proposed immunodevice successfully fulfilled the highly sensitive detection of CEA with a linear range of 0.001–50 ng mL−1 and a detection limit of 0.0007 ng mL−1. The resulting 3D microfluidic origami ECL immunodevice exhibited great promise in the point-of-care diagnostics application of clinical screening of tumor markers.

This work described that one-step synthesis three dimensional anatase hierarchically cactus-like TiO

Rutile titanium dioxide (TiO2 ) is a promising photocatalyst due to its high thermodynamic stability and few intragrain defects. However, it has not yet achieved photocatalytic activity comparable to that of anatase TiO2 owing to its higher recombination rate of electron-hole pairs. To effectively separate the electron-hole pairs in rutile TiO2 , a facet heterojunction (FH) structure to prolong the lifetime of the photogenerated electrons is proposed. Ultrathin TiO2 nanosheets with different facets are coated in situ onto TiO2 nanorod (NR) substrates, where FHs are built among the nanosheets as well as between the nanosheets and NR substrates. The as-prepared rutile TiO2 , with an FH structure (FH-TiO2 ), serves as an effective photocatalyst for water splitting. More than 45 and 18 times higher photogenerated current density and H2 production rate, respectively, are obtained compared to those of pure rutile TiO2 NRs. Moreover, FH-TiO2 delivers a 0.566 mmol g-1 h-1 H2 production rate even in pure water. This study offers important insights into the rational design of rutile TiO2 structures for highly efficient photocatalytic reactions. Accepted version

A platelike tungsten trioxide (WO3) sensitized with CdS quantum dots (QDs) heterojunction is developed for solar-driven, real-time, and selective photoelectrochemical (PEC) sensing of H2O2 in the living cells. The structure is synthesized by hydrothermally growing platelike WO3 on fluorine doped tin oxide (FTO) and subsequently sensitized with CdS QDs. The as-prepared WO3-CdS QDs heterojunction achieve significant photocurrent enhancement, which is remarkably beneficial for light absorption and charge carrier separation. Based on the enzymatic etching of CdS QDs enables the activation of quenching the charge transfer efficiency, thus leading to sensitive PEC recording of H2O2 level in buffer and cellular environments. The results indicated that the proposed method will pave the way for the development of excellent PEC sensing platform with the quantum dot sensitization. This study could also provide a new train of thought on designing of self-operating photoanode in PEC sensing, promoting the application of semiconductor nanomaterials in photoelectrochemistry.