Heat-induced transformation of nickel-coated polycrystalline diamond film studied in situ by XPS and NEXAFS

• Olga V. Sedelnikova,
• Yuliya V. Fedoseeva,
• Dmitriy V. Gorodetskiy,
• Yuri N. Palyanov,
• Elena V. Shlyakhova,
• Eugene A. Maksimovskiy,
• Anna A. Makarova,
• Lyubov G. Bulusheva and
• Aleksandr V. Okotrub

Beilstein J. Nanotechnol. 2025, 16, 887–898, doi:10.3762/bjnano.16.67

• . Keywords: graphitization; near-edge X-ray absorption fine structure spectroscopy; nickel coating; polycrystalline diamond film; single-crystal diamond; X-ray photoelectron spectroscopy; Introduction Diamond and graphite, both composed entirely of carbon atoms, exhibit vastly different properties due to

Scanning tunneling microscopy and spectroscopy of rubrene on clean and graphene-covered metal surfaces

• Karl Rothe,
• Alexander Mehler,
• Nicolas Néel and
• Jörg Kröger

Beilstein J. Nanotechnol. 2020, 11, 1157–1167, doi:10.3762/bjnano.11.100

• near-edge X-ray absorption fine structure spectroscopy [15]. The observed chirality, R-C42H28 and L-C42H28, therefore results from the left or right pair of phenyl groups of a twisted C42H28 molecule being closer to the surface. On Au(111) the formation of homochiral clusters led to remarkable

Triptycene-terminated thiolate and selenolate monolayers on Au(111)

• Jinxuan Liu,
• Martin Kind,
• Björn Schüpbach,
• Daniel Käfer,
• Stefanie Winkler,
• Wenhua Zhang,
• Andreas Terfort and
• Christof Wöll

Beilstein J. Nanotechnol. 2017, 8, 892–905, doi:10.3762/bjnano.8.91

• comprehensively studied using ultra-high vacuum infrared reflection absorption spectroscopy, X-ray photoelectron spectroscopy, near-edge X-ray absorption fine structure spectroscopy and thermal desorption spectroscopy. Due to packing effects, the molecules in all monolayers are substantially tilted. In the

Rigid multipodal platforms for metal surfaces

• Michal Valášek,
• Marcin Lindner and
• Marcel Mayor

Beilstein J. Nanotechnol. 2016, 7, 374–405, doi:10.3762/bjnano.7.34

• were characterized by XPS, Fourier transform infrared absorption spectroscopy (FT-IRRAS), near-edge X-ray absorption fine structure spectroscopy (NEXAFS), and a scanning tunneling microscopy (STM) analysis. As revealed by XPS and NEXAFS analysis, the monolayers derived from the thiol-terminated

Organic and inorganic–organic thin film structures by molecular layer deposition: A review

• Pia Sundberg and
• Maarit Karppinen

Beilstein J. Nanotechnol. 2014, 5, 1104–1136, doi:10.3762/bjnano.5.123

• -diamine and terephthaloyl dichloride to grow semi-aromatic polyamide thin films. The highest achieved growth rate of this type of polyamide on Si(100) substrates was only 2 Å per cycle at 85 °C. The near-edge X-ray absorption fine structure spectroscopy measurements showed that the oligomer units of the

Towards atomic resolution in sodium titanate nanotubes using near-edge X-ray-absorption fine-structure spectromicroscopy combined with multichannel multiple-scattering calculations

• Carla Bittencourt,
• Peter Krüger,
• Maureen J. Lagos,
• Xiaoxing Ke,
• Gustaaf Van Tendeloo,
• Chris Ewels,
• Polona Umek and
• Peter Guttmann

Beilstein J. Nanotechnol. 2012, 3, 789–797, doi:10.3762/bjnano.3.88

• Functional Materials, Albert-Einstein-Str. 15, 12489 Berlin, Germany 10.3762/bjnano.3.88 Abstract Recent advances in near-edge X-ray-absorption fine-structure spectroscopy coupled with transmission X-ray microscopy (NEXAFS–TXM) allow large-area mapping investigations of individual nano-objects with spectral

• resolution in similar techniques with lower spectral resolution [9][10]. We investigate here the electronic structure of sodium titanate nanotubes ((Na,H)TiNTs) by means of near-edge X-ray-absorption fine-structure spectroscopy (NEXAFS) coupled with first-principles NEXAFS calculations (density functional

• oxygen bonding within individual layers of the (Na,H)TiNT. In summary, we have shown that near-edge X-ray-absorption fine-structure spectroscopy combined with transmission X-ray microscopy (NEXAFS–TXM) is a powerful technique to investigate the electronic structure of titanate nanostructures when