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Electrochemical CO 2 reduction (CO 2 RR) to produce high value-added chemicals or fuels is a promising technology to address the greenhouse effect and energy challenges. Formate is a desirable product of CO 2 RR with great economic value. Here, nitrogen-doped bismuth nanosheets (N-BiNSs) were prepared by a facile one-step method. The N-BiNSs were used as efficient electrocatalysts for CO 2 RR with selective formate production. The N-BiNSs exhibited a high formate Faradic efficiency (FE formate) of 95.25% at -0.95 V (vs. RHE) with a stable current density of 33.63 mA cm -2 in 0.5 M KHCO 3 . Moreover, the N-BiNSs for CO 2 RR yielded a large current density (300 mA cm -2 ) for formate production in a flow-cell measurement, achieving the commercial requirement. The FE formate of 90% can maintain stability for 14 h of electrolysis. Nitrogen doping could induce charge transfer from the N atom to the Bi atom, thus modulating the electronic structure of N-Bi nanosheets. DFT results demonstrated the N-BiNSs reduced the adsorption energy of the *OCHO intermediate and promoted the mass transfer of charges, thereby improving the CO 2 RR with high FE formate . This study provides a valuable strategy to enhance the catalytic performance of bismuth-based catalysts for CO 2 RR by using a nitrogen-doping strategy.

It remains a great challenge to develop effective strategies for improving the weak cathodic electrogenerated chemiluminescence (ECL) of the luminol-dissolved O 2 system. Interface modulation between metal and supports is an attractive strategy to improve oxygen reduction reaction (ORR) activity. Therefore, the design of electrocatalysts via interface modulation would provide new opportunities for the ECL amplification involving reactive oxygen species (ROSs). Herein, we have fabricated an Ag single-atom catalyst with an oxygen-bridged interface (Ag-O-Co) through the electrodeposition of Ag on a CoAl layered double hydroxide (LDH) modified indium tin oxide (ITO) electrode (Ag s /LDH/ITO). Interestingly, it was found that the cathodic ECL intensity of the luminol-dissolved O 2 system at the Ag s /LDH/ITO electrode was extraordinarily enhanced in comparison with those at bare ITO and other Ag nanoparticle-based electrodes. The enhanced ECL performances of the Ag s /LDH/ITO electrode were attributed to the increasing amounts of ROSs by electrocatalytic ORR in the Ag-O-Co interface. The electron redistribution of Ag and Co bimetallic sites could accelerate electron transfer, promote the adsorption of O 2 , and sufficiently activate O 2 through a four-electron reaction pathway. Finally, the luminol cathodic ECL intensity was greatly improved. Our findings can provide inspiration for revealing the interface effects between metal and supports, and open up a new avenue to improve the luminol cathodic ECL.

In this work, a H-type hydroquinone/O 2 fuel cell was assembled and shows high energy density in neutral phosphate buffer solution at moderate temperature. The anodic material, Ni(OH) 2 /MWCNTs, was synthesized by a one-step hydrothermal synthesis method to oxidize hydroquinone. The cathode material, Pt/MWCNTs, was obtained by an electrodeposition method, and shows great oxygen reduction reaction (ORR) activity. The properties and the morphology of Ni(OH) 2 /MWCNT nanocomposites were characterized by TEM, XPS, EDS-mapping and electrochemical methods, like cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results show that Ni(OH) 2 /MWCNTs can effectively oxidize hydroquinone and play a dominant role in enhancing the fuel cell performance. The nonenzymatic fuel cell possesses a high power density of 0.24 mW cm -2 at a cell potential of 0.49 V., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

The diffusion of target analytes is a determining factor for the sensitivity of a given gas sensor. Surface adsorption results in a low-concentration region near the sensor surface, producing a concentration gradient perpendicular to the surface, and drives a net flux of molecules toward solid reactive reagents on the sensor surface, that is, vertical diffusion. Here, organic semiconductor supramolecules were patterned into micromeshed arrays to integrate vertical and horizontal diffusion pathways. When used as a gas sensor, these arrays have an order of magnitude higher sensitivity than traditional film-based sensors. The sensor sensitivity ramp down with the increase in coverage density of reactive reagents, yielding two linear regions demarcated by 0.3 coverage, which are identified by the experimental results and simulations. The universal nature of template-assisted patterning allows adjustments in the composition, size, and shape of the constituent material, including nanofibers, nanoparticles, and molecules, and thus serves to improve the sensitivity of gas sensors for detecting various volatile organic compounds., (© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Iron can enter the electron-rich cavities of graphitic carbon nitride (g-C 3 N 4 ). On account of this phenomenon, Fe-doped g-C 3 N 4 (Fe-g-C 3 N 4 ) was prepared as a peroxidase mimetic by using one-step pyrolysis of urea and FeCl 3 ·6H 2 O. Compared to g-C 3 N 4 , Fe-g-C 3 N 4 has a large specific surface area due to the presence of mesopores and cracks, a smaller band gap, and a high loading of Fe in its structure. Thus, Fe-g-C 3 N 4 exhibits greater peroxidase activity with a more obvious color change when using 3,3',5,5'-tetramethylbenzidine (TMB) as a substrate in the presence of hydrogen peroxide (H 2 O 2 ). The color of a mixture of TMB and Fe-g-C 3 N 4 gradually deepens with increasing concentrations of H 2 O 2 . Accordingly, a rapid, sensitive, and low-cost colorimetric assay for the detection of H 2 O 2 was developed. After optimization, this method boasts a wide linear dynamic range for H 2 O 2 detection from 0.005 to 400 μM ( r 2 = 0.9971) with a detection limit of 0.005 μM. Because H 2 O 2 is a main product of glucose oxidation by glucose oxidase (GOx), a colorimetric assay for glucose detection was also realized, with a linear dynamic range of 1-1000 μM ( r 2 = 0.9996) and a detection limit of 0.5 μM. These assays were applied to the quantitative detection of H 2 O 2 in milk and glucose in human serum, respectively.

Molybdenum disulfide quantum dots (MoS 2 QDs) are used in a fluorometric method for the determination of folic acid (FA) based on fluorescence quenching. The MoS 2 QDs synthesized by a hydrothermal method possess bright blue fluorescence (with excitation/emission maxima of 325/415 nm), quantum yield of 3.7%, and excellent storage stability in solution (30 days in the refrigerator). Their fluorescence is quenched by FA, and intensity decreases linearly in the 0.1 to 125 μM FA concentration range. The detection limit is 0.1 μM (at S/N = 3), and the relative standard deviation (for n = 5) is 2.8% for 25 μM concentrations of FA. Studies on the quenching mechanism suggest that the effect is due to static quenching. The FA in commercial FA tablets was successfully determined. Graphical abstract Schematic representation of the hydrothermal method for the preparation of molybdenum disulfide quantum dots (MoS 2 QDs) with about 2.7 ± 0.5 nm diameter using Na 2 MoO 4 and L-cysteine as Mo and S sources, and the fluorescence method for the determination of folic acid (FA) based on fluorescence quenching of MoS 2 QDs.

A label-free electrochemical DNA biosensor array was developed as a model system for simultaneous detection of multiplexed DNAs using microlitres of sample. A novel multi-electrode array was comprised of six gold working electrodes and a gold auxiliary electrode, which were fabricated by gold sputtering technology, and a printed Ag/AgCl reference electrode was fabricated by screen-printing technology. The DNA biosensor array for simultaneous detection of the human immunodeficiency virus (HIV) oligonucleotide sequences, HIV-1 and HIV-2, was fabricated in sequence by self-assembling each of two kinds of thiolated hairpin-DNA probes onto the surfaces of the corresponding three working electrodes, respectively. The hybridization events were monitored by square wave voltammetry using methylene blue (MB) as a hybridization redox indicator. The oxidation currents of MB accumulated on the array decreased with increasing the concentration of HIVs due to higher affinity of MB for single strand rather than double strands of DNA. Under the optimized conditions, the peak currents were linear over ranges from 20 to 100 nM for HIV-1 and HIV-2, with the same detection limits of 0.1 nM (S/N=3), respectively. The biosensor array showed a good specificity without the obvious cross-interference. Furthermore, single-base mutation oligonucleotides and random oligonucleotides can be easily discriminated from complementary target DNAs. This work demonstrates that different hairpin-DNA probes can be used to design the label-free electrochemical biosensor array for simultaneous detection of multiplexed DNA sequences for various clinical applications., (Crown Copyright 2009. Published by Elsevier B.V. All rights reserved.)

A label-free and sensitive faradic impedance spectroscopy (FIS) aptasensor based on target-induced aptamer displacement was developed for the determination of lysozyme as a model system. The aptasensor was fabricated by self-assembling the partial complementary single strand DNA (pcDNA)-lysozyme binding aptamer (LBA) duplex on the surface of a gold electrode. To measure lysozyme, the change in interfacial electron transfer resistance of the aptasensor using a redox couple of [Fe(CN)(6)](3-/4-) as the probe was monitored. The introduction of target lysozyme induced the displacement of the LBA from the pcDNA-LBA duplex on the electrode into the solution, decreasing the electron transfer resistance of the aptasensor. The decrease in the FIS signal is linear with the concentration of lysozyme in the range from 0.2 nM to 4.0 nM, with a detection limit of 0.07 nM. The fabricated aptasensor shows a high sensitivity, good selectivity and satisfactory regeneration. This work demonstrates that a high sensitivity of the fabricated aptasensor can be obtained using a relatively short pcDNA. This work also demonstrates that the target-induced aptamer displacement strategy is promising in the design of an electrochemical aptasensor for the determination of lysozyme with good selectivity and high sensitivity.

Electrogenerated chemiluminescence (also called electrochemiluminescence and abbreviated ECL) involves the generation of species at electrode surfaces that then undergo electron-transfer reactions to form excited states that emit light. ECL biosensor, combining advantages offered by the selectivity of the biological recognition elements and the sensitivity of ECL technique, is a powerful device for ultrasensitive biomolecule detection and quantification. Nanomaterials are of considerable interest in the biosensor field owing to their unique physical and chemical properties, which have led to novel biosensors that have exhibited high sensitivity and stability. Nanomaterials including nanoparticles and nanotubes, prepared from metals, semiconductor, carbon or polymeric species, have been widely investigated for their ability to enhance the efficiencies of ECL biosensors, such as taking as modification electrode materials, or as carrier of ECL labels and ECL-emitting species. Particularly useful application of nanomaterials in ECL biosensors with emphasis on the years 2004-2008 is reviewed. Remarks on application of nanomaterials in ECL biosensors are also surveyed.

A homogeneous electrogenerated chemiluminescence (ECL) immunoassay for human immunoglobulin G (hIgG) has been developed using a N-(aminobutyl)-N-ethylisoluminol (ABEI) as luminescence label at gold nanoparticles modified paraffin-impregnated graphite electrode (PIGE). ECL emission was electrochemically generated from the ABEI-labeled anti-hIgG antibody and markedly increased in the presence of hIgG antigen due to forming a more rigid structure of the ABEI moiety. The concentration of hIgG antigen was determined by the increase of ECL intensity at a gold nanoparticles modified PIGE. It was found that the ECL intensity of ABEI in presence of hydrogen peroxide was dramatically enhanced at gold nanoparticles modified PIGE in neutral aqueous solution and the detection limit of ABEI was 2 x 10(-14)mol/L (S/N=3). The integral ECL intensity was linearly related to the concentration of hIgG antigen from 3.0 x 10(-11) to 1.0 x 10(-9)g/mL with a detection limit of 1 x 10(-11)g/mL (S/N=3). The relative standard deviation was 3.1% at 1.0 x 10(-10)g/mL (n=11). This work demonstrates that the enhancement of the sensitivity of ECL and ECL immunoassay at a nanoparticles modified electrode is a promising strategy.