The integration of graphene into microelectronic devices

• Guenther Ruhl,
• Sebastian Wittmann,
• Matthias Koenig and
• Daniel Neumaier

Beilstein J. Nanotechnol. 2017, 8, 1056–1064, doi:10.3762/bjnano.8.107

• the type of metal removal. The first approach is based on the removal of the metal layer during the CVD process by evaporation [26] or agglomeration [27]. However, the evaporation process lowers the graphene quality. The other approach is the implementation of a dissolution–precipitation mechanism of

Selective photocatalytic reduction of CO₂ to methanol in CuO-loaded NaTaO₃ nanocubes in isopropanol

• Tianyu Xiang,
• Feng Xin,
• Jingshuai Chen,
• Yuwen Wang,
• Xiaohong Yin and
• Xiao Shao

Beilstein J. Nanotechnol. 2016, 7, 776–783, doi:10.3762/bjnano.7.69

• was increased to 3 mol/L and 4 mol/L, the ideal morphology of the nanocubes was disrupted and fewer nanocubes were observed. Generally, the SEM image of 2M-NaTaO3 presents the best morphology. He et al. [34] reported a hydrothermal synthesis of NaTaO3 with Ta2O5 powder and NaOH followed a dissolution

• –precipitation mechanism, where the concentration of the NaOH solution played a crucial role on the morphology of the crystal. This was confirmed in our work. Figure 3 shows UV–vis diffuse reflectance spectra and optical absorption edges of NaTaO3 nanocubes prepared with different concentrations of NaOH. From

Hydration of magnesia cubes: a helium ion microscopy study

• Ruth Schwaiger,
• Johannes Schneider,
• Gilles R. Bourret and
• Oliver Diwald

Beilstein J. Nanotechnol. 2016, 7, 302–309, doi:10.3762/bjnano.7.28

• H2O depending on their size and distribution at the sample surface. Comparison between (a) and (b) points to the volume expansion during hydration and hydroxylation, while (c) and (d) show a probable dissolution/precipitation mechanism. (HIM SE images recorded at 30 kV acceleration voltage and (a,c

In situ observation of biotite (001) surface dissolution at pH 1 and 9.5 by advanced optical microscopy

• Chiara Cappelli,
• Daniel Lamarca-Irisarri,
• Jordi Camas,
• F. Javier Huertas and
• Alexander E. S. Van Driessche

Beilstein J. Nanotechnol. 2015, 6, 665–673, doi:10.3762/bjnano.6.67

• the reaction mechanisms under a wide range of experimental conditions. However, this experimental approach is rather unapt to deal with the reactivity of each crystal face, elucidate the face-specific dissolution–precipitation mechanisms and determine the specific location of the secondary mineral

Direct nanoscale observations of the coupled dissolution of calcite and dolomite and the precipitation of gypsum

• Francesco G. Offeddu,
• Jordi Cama,
• Josep M. Soler and
• Christine V. Putnis

Beilstein J. Nanotechnol. 2014, 5, 1245–1253, doi:10.3762/bjnano.5.138

• the rate-controlling step. The resulting gypsum coating partially covered the surface during the experimental duration of a few hours. Keywords: atomic force microscopy (AFM); calcite; dissolution–precipitation; dolomite; gypsum; Introduction The overall process of dissolution of carbonate minerals