Correction: Khan et al. High Mobility Graphene on EVA/PET. Nanomaterials 2022, 12, 331.

The authors wish to make following corrections in this paper [...].

High Mobility Graphene on EVA/PET.

Transparent conductive film on a plastic substrate is a critical component in low cost, flexible and lightweight optoelectronics. CVD graphene transferred from copper- to ethylene vinyl acetate (EVA)/polyethylene terephthalate (PET) foil by hot press lamination has been reported as a robust and affordable alternative to manufacture highly flexible and conductive films. Here, we demonstrate that annealing the samples at 60 ∘C under a flow of nitrogen, after wet etching of copper foil by nitric acid, significantly enhances the Hall mobility of such graphene films. Raman, Scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) were used to evaluate the morphology and chemical composition of the graphene.

Nanostructured micro particles as a low-cost and sustainable catalyst in the recycling of PET fiber waste by the glycolysis method.

Magnetic Mg-Al-O@Fe3O4 micro particles were synthesized by coating nanosized Mg-Al double oxides onto Fe3O4 micro particles. The formed hierarchical structure gave Mg-Al-O@Fe3O4 micro particles a high active surface area, which enabled these micro particles to work efficiently as a catalyst in the glycolysis of poly(ethylene terephthalate) (PET). The bis(hydroxyethyl) terephthalate (BHET) yield reached above 80 mol% in the presence of 0.5 wt% of Mg-Al-O@Fe3O4 micro catalyst in the reaction system within 90 min at 240 °C. After the reaction, Mg-Al-O@Fe3O4 micro catalyst was easily retrieved by a magnetic decantation and can be repetitively used for two times with a high catalytic efficiency. After that, the deactivated Mg-Al-O@Fe3O4 micro catalyst can be regenerated by heat treatment. The regenerated Mg-Al-O@Fe3O4 micro catalyst displays a comparable catalytic performance as that of the virgin catalyst. In addition, the Mg-Al double oxides and Fe3O4 micro particles are low-cost and environmentally benign. Therefore, the Mg-Al-O@Fe3O4 micro catalyst may contribute to an economically and environmentally improved large-scale circular recycling of PET fiber waste.

Experimental investigations into the irregular synthesis of iron(iii) terephthalate metal-organic frameworks MOF-235 and MIL-101.

MOF-235(Fe) and MIL-101(Fe) are two well-studied metal-organic frameworks (MOFs) with dissimilar crystal structures and topologies. Previously reported syntheses of the former show that it has greatly varying surface areas, indicating a lack of phase purity of the products, i.e. the possible presence of both MOFs in the same sample. To find the reason for this, we have tested and modified the commonly used synthesis protocol of MOF-235(Fe), where a 3 : 5 molar ratio of iron(iii) ions and a terephthalic acid linker is heated in a 1 : 1 DMF : ethanol solvent at 80 °C for 24 h. Using XRD and BET surface area (SABET) measurements, we found that it is difficult to obtain a pure phase of MOF-235, as MIL-101 also appears to form during the solvothermal treatment. Comparison of the XRD peak height ratios of the synthesis products revealed a direct correlation between the MOF-235/MIL-101 content and surface area; more MOF-235 yields a lower surface area and vice versa. In general, using a larger (3 : 1) DMF : ethanol ratio than that reported in the literature and a stoichiometric (4 : 3) Fe(iii) : TPA ratio yields a nearly pure MOF-235 product (SABET = 295 m2 g-1, 67% yield). An optimized synthesis procedure was developed to obtain high-surface area MIL-101(Fe) (SABET > 2400 m2 g-1) in a large yield and at a previously unreported temperature (80 °C vs. previously used 110-150 °C). In situ X-ray scattering was utilized to investigate the crystallization of MOF-235 and MIL-101. At 80 °C, only MOF-235 formed and at 85 and 90 °C, only MIL-101 formed.

Evidence for Electron Transfer between Graphene and Non-Covalently Bound π-Systems.

Hybridizing graphene and molecules possess a high potential for developing materials for new applications. However, new methods to characterize such hybrids must be developed. Herein, the wet-chemical non-covalent functionalization of graphene with cationic π-systems is presented and the interaction between graphene and the molecules is characterized in detail. A series of tricationic benzimidazolium salts with various steric demand and counterions was synthesized, characterized and used for the fabrication of graphene hybrids. Subsequently, the doping effects were studied. The molecules are adsorbed onto graphene and studied by Raman spectroscopy, XPS as well as ToF-SIMS. The charged π-systems show a p-doping effect on the underlying graphene. Consequently, the tricationic molecules are reduced through a partial electron transfer process from graphene, a process which is accompanied by the loss of counterions. DFT calculations support this hypothesis and the strong p-doping could be confirmed in fabricated monolayer graphene/hybrid FET devices. The results are the basis to develop sensor applications, which are based on analyte/molecule interactions and effects on doping.

Chemical Bonding to Novel Translucent Zirconias: A Mechanical and Molecular Investigation.

PURPOSE: To investigate direct bonding of a 10-MDP-based cement to two novel translucent yttria-stabilized tetragonal zirconia polycrystal ceramics (4Y-TZP, 5Y-TZP) and observe the influence of thermocycling on this bonding. MATERIALS AND METHODS: Powders of presintered and isostatically pressed 5Y-TZP, 4Y-TZP and 3Y-TZP were mixed with a 10-MDP-based cement (Panavia F 2.0), then stored in deionized water for 48 h at 37°C or thermocycled 10,000 times. Raman spectroscopy and Fourier-transform infrared spectroscopy were used to assess the presence of a functional group (PO32-) that could indicate bonding before and after thermocycling. X-ray photoelectron spectroscopy was used to identify the presence of the suspected Zr-O-P bond in the same specimens. A shear-bond strength (SBS) test was conducted based on ISO 29022:2013. RESULTS: Marked peaks assigned to the asymmetric vibrations of the PO32- functional group were observed in both zirconias before and after thermocycling. The binding energy corresponding to Zr-O-P interactions (531.5 eV) was masked by the aluminosilicate in the filler of the cement. Shear bond strengths were approximately 20 MPa after water storage and approximately 6 MPa after thermocycling. No differences were found between the control group and the translucent zirconias. CONCLUSION: Direct bonding of the 10-MDP-based cement to both 4Y-TZP and 5Y-TZP was highly plausible. Both 4Y-TZP and 5Y-TZP may be promising alternatives to glass-ceramic restorations.