2 g of KMnO4 was dissolved in the solution (20 mL) with 1 M ClO4 − as the doping anion (we used HClO4 as the source of ClO4 −). The organic solution was added into aqueous solutions slowly, and the mixture was kept overnight Selleck CBL0137 until the reactions conducted completely. The products were then washed with ultrapure water and centrifuged twice to remove residual benzene and KMnO4. Finally, the products were dried in the air for the latter use. Preparation of the electrode The composites were mixed with acetylene black (15 wt.%) and dispersed in 0.5 mL of anhydrous ethanol solution by sonication for 5 min. The mixtures were then cast onto a polished glassy carbon electrode and fasten with 2 μL of

nafion ethanol solution (1% V/V). The electrodes were dried in the air for latter testing. Characterization The morphology of the sample was characterized by scanning electron microscopy (SEM, JSM-6700 F, JEOL Ltd., Akishima-shi, Japan) at an accelerating voltage of 10 kV. Transmission electron microscope (TEM) micrographs are Selleck SIS3 taken with a JEOL2100 TEM (JEOL Ltd., Akishima-shi, Japan) operating at 200 kV. X-ray diffraction (XRD) patterns were collected using X-ray powder diffraction (XRD, Bruker D8 Advance X-ray diffractometer, Bruker AXS, Inc., Madison, WI, USA; Cu

Kα radiation λ=1.5418 Å) at a scan rate of 0.02 s−1. Fourier transform infrared spectroscopy (FTIR) analyses were carried out using a Vertex 70 FTIR spectrophotometer (Bruker AXS, Inc., Madison, WI, USA). A CHI 760C electrochemical workstation (CHI Instruments, Austin, TX, USA) was used to collect electrochemical data. All electrochemical experiments were conducted in a three-electrode cell, in which a 1.5×1.5 cm2 Pt plate was used as the counter electrode and a saturated calomel electrode Venetoclax supplier was selected as the reference electrode. Results and discussion The schematic of MnO2/PANI fabrication procedure is shown in Figure 1. The reaction commences at the interface of the two solutions immediately as the aniline solution is carefully spread onto the aqueous solution of KMnO4. The interfacial polymerization does not terminate until KMnO4 or aniline is

consumed completely. The products diffuse into the aqueous solution spontaneously due to the doping procedure of the polymers and hydrophilic property of hydrate MnO2. The color of the products in different solutions (a to e: 1, 0.5, 0.2, 0.1, and 0 M HClO4, respectively, as shown in the inset of Figure 1) turns from green to brown. This color evolvement is attributed to the different components of composites accompanying with the change of PANI-doping degree. The SEM and TEM images, FTIR spectra, and XRD patterns were employed to investigate the components and the formation of the products. this website Figure 1 The schematic of the synthesis procedure and the morphologies of MnO 2 /PANI composites at different HClO 4 concentrations.