Recent progress in perovskite solar cells: the perovskite layer

• Xianfeng Dai,
• Ke Xu and
• Fanan Wei

Beilstein J. Nanotechnol. 2020, 11, 51–60, doi:10.3762/bjnano.11.5

• organic cation, M2+ is a divalent metal, and X− is a halide anion [57]. The overall 2D structure is stabilized via van der Waals interactions. Importantly, the 2D perovskite structure can also be considered as a multiple-quantum-well structure, which obviously suppresses the ion migration that is evident

Ultrasonication-assisted synthesis of CsPbBr₃ and Cs₄PbBr₆ perovskite nanocrystals and their reversible transformation

• Longshi Rao,
• Xinrui Ding,
• Xuewei Du,
• Guanwei Liang,
• Yong Tang,
• Kairui Tang and
• Jin Z. Zhang

Beilstein J. Nanotechnol. 2019, 10, 666–676, doi:10.3762/bjnano.10.66

• by [PbX6]4− octahedra in which the Cs+ ions reside in the periphery of this network [9][10]. These PNCs are prone to structural instabilities and phase transformations involving ion migration and interface hydration [11]. However, this phase and structure versatility has become the great advantage of

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

• accumulate near the crystal surface due to band bending effects. Time-dependent changes of the surface potential occurring under illumination on the scale of a few seconds reveal the existence of slow ion-migration mechanisms. Lastly, photopotential decay at the sub-millisecond time scale related to the

• . Keywords: carrier lifetime; ion migration; Kelvin probe force microscopy (KPFM); noncontact atomic force microscopy (nc-AFM); organic–inorganic hybrid perovskites; photostriction; single crystals; surface photovoltage (SPV); time-resolved surface photovoltage; Introduction Organic–inorganic hybrid

• the photocarrier transport on the sole basis of KPFM data. This uncertainty is largely due to the contributions of the ionic species to the surface potential contrasts [6][8][9][10]. Time-resolved measurements have especially shown that intra-grain ion-migration mechanisms [9] can significantly impact

Correlative electrochemical strain and scanning electron microscopy for local characterization of the solid state electrolyte Li_1.3Al_0.3Ti_1.7(PO₄)₃

• Nino Schön,
• Deniz Cihan Gunduz,
• Shicheng Yu,
• Hermann Tempel,
• Roland Schierholz and
• Florian Hausen

Beilstein J. Nanotechnol. 2018, 9, 1564–1572, doi:10.3762/bjnano.9.148

• area (typically in the range of 1 cm2). Hence, only averaged values are obtained whilst locally the ion mobility can still be inhomogeneous [11]. Translating local ion migration into global conductivity is part of ongoing research. First approaches for small-scale impedance measurements have been

• -ion mobility in Li0.33La0.56TiO3 using scanning electron microscopy (SEM) with electron backscatter diffraction (EBSD) and electrochemical strain microscopy (ESM) [21]. The authors correlate variations in the Li-ion mobility detected by ESM with limitations in the Li-ion migration pathway. ESM is a

• surface, causing a strain of the material according to Vegard’s Law [25]. In the case of a solid state electrolyte, with its inherently low electronic conductivity, it remains arguable if the ESM amplitude signal is predominantly caused by ion migration. Very recently, Lushta et al. [28] presented ESM

Magnesium batteries: Current state of the art, issues and future perspectives

• Rana Mohtadi and
• Fuminori Mizuno

Beilstein J. Nanotechnol. 2014, 5, 1291–1311, doi:10.3762/bjnano.5.143

• mobility. This was attributed to the strong coulombic interactions with BH4− resulting from the small cage size. They proposed that increasing the cage size, by partial substitution of BH4− with the larger AlH4−, may enable magnesium ion migration, however, this was not experimentally demonstrated. Another

Parallel- and serial-contact electrochemical metallization of monolayer nanopatterns: A versatile synthetic tool en route to bottom-up assembly of electric nanocircuits

• Jonathan Berson,
• Assaf Zeira,
• Rivka Maoz and
• Jacob Sagiv

Beilstein J. Nanotechnol. 2012, 3, 134–143, doi:10.3762/bjnano.3.14

• –solution interface by ion migration to the electrode rather than by electron transfer to hydrated ions in solution. Keywords: AFM (SFM); bipolar electrochemistry; electrochemical metal deposition; monolayer patterning; nanolithography; self-assembled organosilane monolayers; Introduction The quest for a