One-step synthesis of carbon-supported electrocatalysts

• Sebastian Tigges,
• Nicolas Wöhrl,
• Ivan Radev,
• Ulrich Hagemann,
• Markus Heidelmann,
• Thai Binh Nguyen,
• Stanislav Gorelkov,
• Stephan Schulz and
• Axel Lorke

Beilstein J. Nanotechnol. 2020, 11, 1419–1431, doi:10.3762/bjnano.11.126

• explained by the aforementioned removal of carbon at the Pt-NPs surface and slower degradation of the Pt/CNW catalysts as observed in Figure 8. However, the degradation mechanisms behind the ECSA loss on both Pt/CNW and HiSPEC4000 are quite similar, as seen from the exponential decay of ECSA in Figure 8. In

Quantitative analysis of annealing-induced instabilities of photo-leakage current and negative-bias-illumination-stress in a-InGaZnO thin-film transistors

• Dapeng Wang and
• Mamoru Furuta

Beilstein J. Nanotechnol. 2019, 10, 1125–1130, doi:10.3762/bjnano.10.112

• before and after 104 s NBIS without and with a 10 V gate pulse; (d) hysteresis of IGZO TFTs as a function of NBIS duration. Possible degradation mechanisms of NBIS-induced instability in the devices annealed at (a) 300, (b) 350, and (c) 400 °C, respectively. The electrical parameters of a-IGZO TFTs

Nanocomposite–parylene C thin films with high dielectric constant and low losses for future organic electronic devices

• Marwa Mokni,
• Gianluigi Maggioni,
• Abdelkader Kahouli,
• Sara M. Carturan,
• Walter Raniero and
• Alain Sylvestre

Beilstein J. Nanotechnol. 2019, 10, 428–441, doi:10.3762/bjnano.10.42

• candidate as a coating dielectric material to protect the sensitive organic layer from oxygen and water vapor [28], which are among the greatest degradation mechanisms contributing to the electrical instability of OFETs [29][30][31][32] and oxide TFTs [33]. It is inferred that parylene C presents a broad

Multimodal noncontact atomic force microscopy and Kelvin probe force microscopy investigations of organolead tribromide perovskite single crystals

• Yann Almadori,
• David Moerman,
• Jaume Llacer Martinez,
• Philippe Leclère and
• Benjamin Grévin

Beilstein J. Nanotechnol. 2018, 9, 1695–1704, doi:10.3762/bjnano.9.161

• (BELSPO-PAI VII/5), the FRS-FNRS PDR Project “Hybrid Organic/Inorganic Nanomaterials for Energy COnversion and STOrage Devices on FLEXible and Stretchable Substrates (ECOSTOFLEX)”, and MP 1307 COST Action “Stable Next-Generation Photovoltaics: Unraveling Degradation Mechanisms of Organic and Perovskite

Sugarcane juice derived carbon dot–graphitic carbon nitride composites for bisphenol A degradation under sunlight irradiation

• Lan Ching Sim,
• Jing Lin Wong,
• Chen Hong Hak,
• Jun Yan Tai,
• Kah Hon Leong and
• Pichiah Saravanan

Beilstein J. Nanotechnol. 2018, 9, 353–363, doi:10.3762/bjnano.9.35

• (PL), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), etc. The influence of the weight percentage of CDs and a scavenging experiment were carried out to illustrate the potential degradation mechanisms. Overall, the incorporation of CDs into g-C3N4 was efficient towards

Multiscale modeling of lithium ion batteries: thermal aspects

• Arnulf Latz and
• Jochen Zausch

Beilstein J. Nanotechnol. 2015, 6, 987–1007, doi:10.3762/bjnano.6.102

The cell-type specific uptake of polymer-coated or micelle-embedded QDs and SPIOs does not provoke an acute pro-inflammatory response in the liver

• Markus Heine,
• Alexander Bartelt,
• Oliver T. Bruns,
• Denise Bargheer,
• Artur Giemsa,
• Barbara Freund,
• Ludger Scheja,
• Christian Waurisch,
• Alexander Eychmüller,
• Rudolph Reimer,
• Horst Weller,
• Peter Nielsen and
• Joerg Heeren

Beilstein J. Nanotechnol. 2014, 5, 1432–1440, doi:10.3762/bjnano.5.155

• the mononuclear phagocytic system (MPS) [7]. Consequently, larger nanocrystals are exposed to cellular degradation mechanisms of macrophages, e.g., the acidic environment of lysosomes and even more harsh conditions in phagosomes containing also hydrogen peroxide [8]. This might disrupt the surface

Design criteria for stable Pt/C fuel cell catalysts

• Josef C. Meier,
• Carolina Galeano,
• Ioannis Katsounaros,
• Jonathon Witte,
• Hans J. Bongard,
• Angel A. Topalov,
• Claudio Baldizzone,
• Stefano Mezzavilla,
• Ferdi Schüth and
• Karl J. J. Mayrhofer

Beilstein J. Nanotechnol. 2014, 5, 44–67, doi:10.3762/bjnano.5.5

• in particular the catalyst stability are evaluated. Based on our results, a set of design criteria for more stable and active Pt/C and Pt-alloy/C materials is suggested. Keywords: catalyst design criteria; degradation mechanisms; fuel cell catalyst; nanoparticles; stability; Introduction The

• factors that influence the activity of the catalyst was obtained in recent years such as alloying platinum with transition metals [4][5][6][7] or varying the particle size [8][9][10][11][12][13][14], many questions regarding the fundamental degradation mechanisms of such systems remain [15][16]. A stable

• observed platinum surface area loss. For standard Pt/C catalysts, indications for a variety of different degradation mechanisms are reported and summarized in the literature [3][15][16][17][40][41][42]. In Figure 1 we provide a short summary of catalyst degradation mechanisms that have been suggested to