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The development of electrocatalysts with high activity and low cost has attracted growing attentions in recent years. Herein, we reported the Mn-doped CoP nanosheet arrays on flexible activated carbon cloth (Mn–CoP/CC) for the effective oxygen evolution reaction (OER) at low overpotential and high current density. Due to the novel 3D nanostructures of the carbon cloth and doping effect of the Mn element, the Mn doped CoP/CC electrode delivered the best overpotential of 317 mV for water splitting with the current density of 10 mA/cm2, a Tafel slope of ∼65.1 mV/dec, and excellent stability over 16 h in 1.0 mol/L KOH, which is superior or comparable to the most of the reported cobalt-based catalysts. Thus outstanding electrocatalytic performance originates from the Mn doping effect, which resulted in increased surface area and fast charge-transfer. It is believed that these findings would help us to develop high effective and stable electrocatalysts for water splitting.

Porous carbon nanomaterials with significant capacitive performance were successfully prepared through a simple two-step process of thermal-polymerization and carbonization without an additional template. As a result, the as-prepared porous carbon nanomaterials of sample-A and sample-B exhibited an amorphous phase with low graphitization. And sample-A showed a moderate specific surface area of 476.39 m2/g, larger than that of sample-B (280.94 m2/g). The relatively high mass specific capacitance of 205.1 F/g at a scan rate of 5 mV/s and 211 F/g at a current density of 4 A/g was obtained by sample-A, which are higher than those of sample-B (82.6 F/g at 5 mV/s and 78.6 F/g at 4 A/g). Sample-A also showed excellent conductivity and superior cyclic stability with 94.19% capacitance retention after 5000 cycles, which are also higher than those of sample-B. This work proposed a cost-effective, green, and promising strategy for the large-scale preparation of porous carbon nanomaterial electrodes.

Particulate matter is one of the main pollutants, causing hazy days, and it has been serious concern for public health worldwide, particularly in China recently. Quality of outdoor atmosphere with a pollutant emission of PM2.5 is hard to be controlled; but the quality of indoor air could be achieved by using fibrous membrane-based air-filtering devices. Herein, we introduce nanofiber membranes for both indoor and outdoor air protection by electrospun synthesized polyacrylonitrile:TiO2 and developed polyacrylonitrile-co-polyacrylate:TiO2 composite nanofiber membranes. In this study, we design both polyacrylonitrile:TiO2 and polyacrylonitrile-co-polyacrylate:TiO2 nanofiber membranes with controlling the nanofiber diameter and membrane thickness and enable strong particulate matter adhesion to increase the absorptive performance and by synthesizing the specific microstructure of different layers of nanofiber membranes. Our study shows that the developed polyacrylonitrile-co-polyacrylate:TiO2 nanofiber membrane achieves highly effective (99.95% removal of PM2.5) under extreme hazy air-quality conditions (PM2.5 mass concentration 1 mg/m3). Moreover, the experimental simulation of the test in 1 cm3 air storehouse shows that the polyacrylonitrile-co-polyacrylate:TiO2 nanofiber membrane (1 g/m2) has the excellent PM 2.5 removal efficiency of 99.99% in 30 min.

Surfactant-free and low Au loading Cu2O@Au and Au hollow cubes, based on electrodeposited Cu2O cubes as sacrificed templates, were prepared by means of a galvanic replacement reaction (GRR). The electrocatalytical performance of the as-prepared catalysts towards carbon dioxide (CO2) electrochemical reduction was evaluated. The experimental results show that Cu2O@Au catalyst can convert CO2 to carbon monoxide (CO) with a maximum Faradaic efficiency (FE) of ~ 30.1% at the potential of − 1.0 V (vs. RHE) and is about twice the FE of the other catalysts at the same potential. By comparison, such electrocatalytical enhancement is attributed to the metal-oxide interface in Cu2O@Au.

The authors describe a simplified chemical precipitation method and silver mirror reaction to synthesize a nanocomposite consiting of silver nanoparticles on a thin and porous nickel oxide film. Placed on a glassy carbon electrode (GCE), it allows for the determination of levofloxacin (LEV) via square wave voltammetry (SWV). Under optimal detection conditions, the voltammetric signal (typically measured at around 0.96 V vs. SCE) increases linearly in the 0.25-100 μM LEV concentration range. And the detection limit was calculated as 27 nM (at S/N = 3). The sensor is highly selective, stable and repeatable. It was applied to the determination of LEV in spiked human serum samples, and the satisfactory results confirm the applicability of this sensor to practical analyses. Graphical abstract Schematic of a two-step method to synthesize a nanocomposite consisting of nickel oxide porous thin-film supported silver nanoparticles. The composite was used for improved voltammetric determination of levofloxacin.