Karsten Kunze
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Karsten Kunze has a total of 257 co-authors. Here are the top co-authors by number of shared publications:
Luigi Burlini
Geological Institute, ETH-Zürich, Sonneggstrasse 5 8092, Zürich, Switzerland
10 shared publications- Misha Bystricky
Institut de Recherche en Astrophysique et Planétologie (IRAP) CNRS‐CNES‐Université de Toulouse III Observatoire Midi‐Pyrénées Toulouse France
7 shared publications - Jean-Pierre Burg
Department of Earth Sciences ETH Zurich Zurich Switzerland
5 shared publications Brent L. Adams
Brigham Young University
4 shared publicationsHolger Stünitz
Department of Geosciences, Basel University, Bernoullistr. 30-32, CH-4056 Basel, Switzerland
4 shared publications- Rainer Abart
Department of Lithospheric Research University of Vienna Vienna Austria
4 shared publications
Latest Publications
- Open Access
- 9 September 2026
- Published by Wiley in Small Methods
- Vol. 10 (19) , e71029
Nanosecond, Nanometer Movies of MEMS/NEMS Dynamics in a Standard SEM Using Time‐Tagged Secondary Electrons
Dynamic phenomena at the micro‐ and nanoscale underpin technologies ranging from micro‐ and nanoelectromechanical systems (MEMS/NEMS) actuators and sensors to quantum instrumentation and communication hardware. In this paper, we demonstrate that time‐resolved full‐field scanning electron microscopy (SEM) for periodically driven micro‐ and nanostructures offers access to their spatiotemporal dynamics. This is achieved using a conventional SEM operated with its continuous electron beam and combined with a multi‐channel plate (MCP) with a time‐to‐digital converter (TDC) for time‐resolved measurements. Effective frame rates from to frames per second are reached and motion tracking with nm spatial and ns temporal jitter is demonstrated, enabling access to both micrometer‐scale and nanometer‐scale motion. By bringing high temporal resolution to widely available electron microscopes without invasive column modifications, this approach enables a broad range of experiments on dynamic micro‐ and nanomechanical systems.
- 9 September 2026
- Published by Wiley in Small Methods
- Vol. 10 (19) , e71029
Open AccessNanosecond, Nanometer Movies of MEMS/NEMS Dynamics in a Standard SEM Using Time‐Tagged Secondary Electrons
Dynamic phenomena at the micro‐ and nanoscale underpin technologies ranging from micro‐ and nanoelectromechanical systems (MEMS/NEMS) actuators and sensors to quantum instrumentation and communication hardware. In this paper, we demonstrate that time‐resolved full‐field scanning electron microscopy (SEM) for periodically driven micro‐ and nanostructures offers access to their spatiotemporal dynamics. This is achieved using a conventional SEM operated with its continuous electron beam and combined with a multi‐channel plate (MCP) with a time‐to‐digital converter (TDC) for time‐resolved measurements. Effective frame rates from to frames per second are reached and motion tracking with nm spatial and ns temporal jitter is demonstrated, enabling access to both micrometer‐scale and nanometer‐scale motion. By bringing high temporal resolution to widely available electron microscopes without invasive column modifications, this approach enables a broad range of experiments on dynamic micro‐ and nanomechanical systems.
- Open Access
- 6 December 2023
- Published by Wiley in Advanced Science
- Vol. 11 (5) , e2305366
Probing the Intrinsic Strain in Suspended Graphene Films Using Electron and Optical Microscopy
Quantifying the intrinsic properties of 2D materials is of paramount importance for advancing their applications. Large‐scale production of 2D materials merits the need for approaches that provide direct information about the role of growth substrate on 2D material properties. Transferring the 2D material from its growth substrates can modify the intrinsic properties of the asgrown 2D material. In this study, suspended chemical vapor deposition (CVD) graphene films are prepared directly on their growth substrates in a high‐density grid array. The approach facilitates the quantification of intrinsic strain and doping in suspended CVD graphene films. To achieve this, transmission electron microscopy and large‐area Raman mapping are employed. Remarkably, the analysis reveals consistent patterns of compressive strain (≈−0.2%) both in the diffraction patterns and Raman maps obtained from these suspended graphene films. By conducting investigations directly on the growth substrates, the potential influences introduced during the transfer process are circumvented effectively. Consequently, the methodology offers a robust and reliable means of studying the intrinsic properties of 2D materials in their authentic form, uninfluenced by the transfer‐induced alterations that may skew the interpretation of their properties.
- 6 December 2023
- Published by Wiley in Advanced Science
- Vol. 11 (5) , e2305366
Open AccessProbing the Intrinsic Strain in Suspended Graphene Films Using Electron and Optical Microscopy
Quantifying the intrinsic properties of 2D materials is of paramount importance for advancing their applications. Large‐scale production of 2D materials merits the need for approaches that provide direct information about the role of growth substrate on 2D material properties. Transferring the 2D material from its growth substrates can modify the intrinsic properties of the asgrown 2D material. In this study, suspended chemical vapor deposition (CVD) graphene films are prepared directly on their growth substrates in a high‐density grid array. The approach facilitates the quantification of intrinsic strain and doping in suspended CVD graphene films. To achieve this, transmission electron microscopy and large‐area Raman mapping are employed. Remarkably, the analysis reveals consistent patterns of compressive strain (≈−0.2%) both in the diffraction patterns and Raman maps obtained from these suspended graphene films. By conducting investigations directly on the growth substrates, the potential influences introduced during the transfer process are circumvented effectively. Consequently, the methodology offers a robust and reliable means of studying the intrinsic properties of 2D materials in their authentic form, uninfluenced by the transfer‐induced alterations that may skew the interpretation of their properties.
- Open Access
- 23 March 2022
- Published by Royal Society of Chemistry (RSC) in Energy & Environmental Science
- Vol. 15 (5) , 2002-2010
Crystal orientation-dependent etching and trapping in thermally-oxidised Cu2O photocathodes for water splitting
Crystal orientation-dependent etching, charge-carrier trapping behaviour, and performance of single-crystal photocathodes are enabled by ammonia solution etching of thermally-oxidised Cu2O.
- 23 March 2022
- Published by Royal Society of Chemistry (RSC) in Energy & Environmental Science
- Vol. 15 (5) , 2002-2010
Open AccessCrystal orientation-dependent etching and trapping in thermally-oxidised Cu2O photocathodes for water splitting
Crystal orientation-dependent etching, charge-carrier trapping behaviour, and performance of single-crystal photocathodes are enabled by ammonia solution etching of thermally-oxidised Cu2O.
- Open Access
- 13 May 2019
- Published by Springer Nature in Contributions to Mineralogy and Petrology
- Vol. 174 (5) , 46
Species diffusion in clinopyroxene solid solution in the diopside–anorthite system
The coupled multicomponent diffusion of the species Ca2Si2O6, CaAl2SiO6 and Mg2Si2O6 was determined in diopside crystals in the diopside/anorthite (Di/An) system at temperatures (T) of 1110–1260 °C and oxygen fugacities (fO2) between 1.0 log unit below and above the fayalite–magnetite–quartz equilibrium (FMQ ± 1). Diffusion couples were prepared by the seed overgrowth technique. Element concentration profiles were measured perpendicular to the rim/core interface by step-scanning profiling with a field emission gun scanning electron microscope (FEG-SEM). The multicomponent diffusion matrix was solved by fitting its eigenvalues (λ) and eigenvectors (v) to the measured concentration profiles. The full diffusion matrix D can be recovered by using the formula \(D = P\varLambda P^{ - 1}\) resulting in the following equation: $$D_{\text{Di/An}} = \left[ {\begin{array}{*{20}c} {1.00} & { - 0.67} \\ { - 0.38} & {1.00} \\ \end{array} } \right]\left[ {\begin{array}{*{20}c} {\lambda 1\left( T \right)} & 0 \\ 0 & {\lambda 2\left( T \right)} \\ \end{array} } \right]\left[ {\begin{array}{*{20}c} {1.00} & { - 0.67} \\ { - 0.38} & {1.00} \\ \end{array} } \right]^{ - 1} .$$ The eigenvalues (λ1 and λ2) represent upper limit values and are described by the following Arrhenius-type equations: $$\lambda 1 \left( {\text{Di/An}} \right) = 10^{ - 15.98 \pm 1.17} \times \exp \left[ {\frac{{ - 114.4 \pm 32.8 {\text{kJ/mol}}}}{RT}} \right],$$ $$\lambda 2 \left( {\text{Di/An}} \right) = 10^{ - 16.23 \pm 1.17} \times { \exp }\left[ {\frac{{ - 114.4 \pm 32.8 {\text{kJ/mol}}}}{RT}} \right],$$ where λ1 and λ2 are the first and second eigenvalue of the diffusion matrix in m2 s−1, R is the gas constant and T is the temperature in K. The dominant eigenvalue (λ1) is one quarter order of magnitude larger than the second eigenvalue (λ2). The eigenvectors are constant for all experiments inferring that the entire D matrix can be described with the eigenvalues as the only T-dependent parameter. Additionally, the derived diffusion data and modeling approach were applied to constrain the duration of magmatic processes recorded in zoned clinopyroxene (cpx) phenocrysts from a basaltic, post-plutonic dyke of the Tertiary Adamello batholiths (N-Italy). The results reveal residence times of the overgrown cpx prior to final emplacement in the range of 0.25–1.7 years (lower limit values) testifying that the data and method can be applied to model cpx diffusion profiles in complex natural cpx.- 13 May 2019
- Published by Springer Nature in Contributions to Mineralogy and Petrology
- Vol. 174 (5) , 46
Open AccessSpecies diffusion in clinopyroxene solid solution in the diopside–anorthite system
The coupled multicomponent diffusion of the species Ca2Si2O6, CaAl2SiO6 and Mg2Si2O6 was determined in diopside crystals in the diopside/anorthite (Di/An) system at temperatures (T) of 1110–1260 °C and oxygen fugacities (fO2) between 1.0 log unit below and above the fayalite–magnetite–quartz equilibrium (FMQ ± 1). Diffusion couples were prepared by the seed overgrowth technique. Element concentration profiles were measured perpendicular to the rim/core interface by step-scanning profiling with a field emission gun scanning electron microscope (FEG-SEM). The multicomponent diffusion matrix was solved by fitting its eigenvalues (λ) and eigenvectors (v) to the measured concentration profiles. The full diffusion matrix D can be recovered by using the formula \(D = P\varLambda P^{ - 1}\) resulting in the following equation: $$D_{\text{Di/An}} = \left[ {\begin{array}{*{20}c} {1.00} & { - 0.67} \\ { - 0.38} & {1.00} \\ \end{array} } \right]\left[ {\begin{array}{*{20}c} {\lambda 1\left( T \right)} & 0 \\ 0 & {\lambda 2\left( T \right)} \\ \end{array} } \right]\left[ {\begin{array}{*{20}c} {1.00} & { - 0.67} \\ { - 0.38} & {1.00} \\ \end{array} } \right]^{ - 1} .$$ The eigenvalues (λ1 and λ2) represent upper limit values and are described by the following Arrhenius-type equations: $$\lambda 1 \left( {\text{Di/An}} \right) = 10^{ - 15.98 \pm 1.17} \times \exp \left[ {\frac{{ - 114.4 \pm 32.8 {\text{kJ/mol}}}}{RT}} \right],$$ $$\lambda 2 \left( {\text{Di/An}} \right) = 10^{ - 16.23 \pm 1.17} \times { \exp }\left[ {\frac{{ - 114.4 \pm 32.8 {\text{kJ/mol}}}}{RT}} \right],$$ where λ1 and λ2 are the first and second eigenvalue of the diffusion matrix in m2 s−1, R is the gas constant and T is the temperature in K. The dominant eigenvalue (λ1) is one quarter order of magnitude larger than the second eigenvalue (λ2). The eigenvectors are constant for all experiments inferring that the entire D matrix can be described with the eigenvalues as the only T-dependent parameter. Additionally, the derived diffusion data and modeling approach were applied to constrain the duration of magmatic processes recorded in zoned clinopyroxene (cpx) phenocrysts from a basaltic, post-plutonic dyke of the Tertiary Adamello batholiths (N-Italy). The results reveal residence times of the overgrown cpx prior to final emplacement in the range of 0.25–1.7 years (lower limit values) testifying that the data and method can be applied to model cpx diffusion profiles in complex natural cpx. - 1 January 2018
- Published by Elsevier in Tectonophysics
- Vol. 722, 566-576
Interpreting magnetic fabrics in amphibole-bearing rocks
- 1 January 2018
- Published by Elsevier in Tectonophysics
- Vol. 722, 566-576
Interpreting magnetic fabrics in amphibole-bearing rocks
- 1 December 2017
- Published by Mineralogical Society of America in American Mineralogist: Journal of Earth and Planetary Materials
- Vol. 102 (12) , 2467-2483
Mineralogical, geochemical, and textural indicators of crystal accumulation in the Adamello Batholith (Northern Italy)
- 1 December 2017
- Published by Mineralogical Society of America in American Mineralogist: Journal of Earth and Planetary Materials
- Vol. 102 (12) , 2467-2483
Mineralogical, geochemical, and textural indicators of crystal accumulation in the Adamello Batholith (Northern Italy)
- 2 June 2017
- Published by Royal Society of Chemistry (RSC) in Materials Horizons
- Vol. 4 (5) , 857-861
Visualising compositional heterogeneity during the scale up of multicomponent zeolite bodies
An unprecedented approach is introduced to compositionally map binder-containing Li-X zeolite sorbents at various stages of the industrial manufacture.
- 2 June 2017
- Published by Royal Society of Chemistry (RSC) in Materials Horizons
- Vol. 4 (5) , 857-861
Visualising compositional heterogeneity during the scale up of multicomponent zeolite bodies
An unprecedented approach is introduced to compositionally map binder-containing Li-X zeolite sorbents at various stages of the industrial manufacture.
- 27 February 2017
- Published by IOP Publishing in Nanotechnology
- Vol. 28 (13) , 135701
Bi-modal nanoheteroepitaxy of GaAs on Si by metal organic vapor phase epitaxy
Nano-heteroepitaxial growth of GaAs on Si(001) by metal organic vapor phase epitaxy was investigated to study emerging materials phenomena on the nano-scale of III–V/Si interaction. Arrays of Si nano-tips (NTs) embedded in a SiO 2 matrix were used as substrates. The NTs had top Si openings of 50–90 nm serving as seeds for the selective growth of GaAs nano-crystals (NCs). The structural and morphological properties were investigated by high resolution scanning electron microscopy, atomic force microscopy, electron backscatter diffraction, x-ray diffraction, and high resolution scanning transmission electron microscopy. The GaAs growth led to epitaxial NCs featuring a bi-modal distribution of size and morphology. NCs of small size exhibited high structural quality and well-defined {111}–{100} faceting. Larger clusters had less regular shapes and contained twins. The present work shows that the growth of high quality GaAs NCs on Si NTs is feasible and can provide an alternate way to the integration of compound semiconductors with Si micro- and opto-electronics technology.
- 27 February 2017
- Published by IOP Publishing in Nanotechnology
- Vol. 28 (13) , 135701
Bi-modal nanoheteroepitaxy of GaAs on Si by metal organic vapor phase epitaxy
Nano-heteroepitaxial growth of GaAs on Si(001) by metal organic vapor phase epitaxy was investigated to study emerging materials phenomena on the nano-scale of III–V/Si interaction. Arrays of Si nano-tips (NTs) embedded in a SiO 2 matrix were used as substrates. The NTs had top Si openings of 50–90 nm serving as seeds for the selective growth of GaAs nano-crystals (NCs). The structural and morphological properties were investigated by high resolution scanning electron microscopy, atomic force microscopy, electron backscatter diffraction, x-ray diffraction, and high resolution scanning transmission electron microscopy. The GaAs growth led to epitaxial NCs featuring a bi-modal distribution of size and morphology. NCs of small size exhibited high structural quality and well-defined {111}–{100} faceting. Larger clusters had less regular shapes and contained twins. The present work shows that the growth of high quality GaAs NCs on Si NTs is feasible and can provide an alternate way to the integration of compound semiconductors with Si micro- and opto-electronics technology.
- Open Access
- 20 December 2016
- Published by Wiley
- p. 932-933
Texture, microstructure and mechanical anisotropy in SLM processed superalloys
- 20 December 2016
- Published by Wiley
- p. 932-933
Open AccessTexture, microstructure and mechanical anisotropy in SLM processed superalloys