This file was created by the TYPO3 extension publications
--- Timezone: CEST
Creation date: 2025-05-03
Creation time: 22:31:07
--- Number of references
156
article
Diethylene Glycol Diethyl Ether (DEGDEE) as Electrolyte Solvent for Reversible Electrochemical Magnesium Plating
2025
3
1
10.1002/celc.202500046
ChemElectroChem
in press
2500046
B.W.
Schick
M.
Uhl
M.
Al-Shakran
J.
Bansmann
S.
Riedel
Z.
Zhao-Karger
T.
Jacob
article
Exploring the Integration of Sulfonated Poly(Phenylene Sulfone) Ionomers into the Cathode Catalyst Layers of Proton Exchange Membrane Fuel Cells
2025
3
1
10.1016/j.jpowsour.2025.236896
Journal of Power Sources
641
236896
D.
Yazili-Marini
L.
Fogang
E.
Marini
T.
Morawietz
G.
Titvinidze
J.
Bansmann
M.
ö
L.
ö
article
Stabilization of Ru-Core Pt-Shell Model Electrodes by Electronic Effects and Electrooxidation Reactions
2025
3
1
10.1002/cctc.202401913
CatChemCat
in press
e202401913
A. K.
Engstfeld
L.
Forschner
M.
ö
L.
Pithan
P.
Beyer
Z.
Jusys
J.
Bansmann
R. J.
Behm
J.
Drnec
article
A novel hybrid biosensor for miRNA detection based on peptide nucleic acids and molecularly imprinted polymers
2025
2
1
10.1016/j.bioelechem.2025.108964
Bioelectrochemistry
165
108964
M.
Abdel-Hamied
M.
Guo
Y.
Wei
J.
Bansmann
R. M.
El Nashar
F.
Oswald
B.
Mizaikoff
C.
Kranz
article
Mechanism of Optical and Electrical H2S Gas Sensing of Pristine and Surface Functionalized ZnO Nanowires
2024
12
12
10.1021/acsomega.4c04412
ACS Omega
9
50188
51
A.
Kaiser
T.
Mauritz
J.
Bansmann
J.
Biskupek
Ulrich
Herr
K.
Thonke
article
Plasma Carbonization of Sustainable Lignin Fiber-Derived Papers for Supercapacitor Electrodes
2024
11
1
10.1002/mame.202400336
Macromolecular Materials and Engineering
310
2400336
3
P. A.
Schuster
C.
Mirle
L.
Kuske
J.
Schmidt
M. R.
Buchmeister
F.
Rohrbach
J.
Bansmann
S.
Terbrack
H.
Heuermann
E.
Frank
A. J. C.
Kuehne
article
Probing coherence properties of shallow implanted NV snsembles under different oxygen terminations
2024
11
10.1088/2633-4356/ad9376
Materials for Quantum Technology
4
041001
4
J.
Fuhrmann
J.
Lang
J.
Scharpf
N.
Striegler
T.
Unden
P.
Neumann
J.
Bansmann
F.
Jelzko
article
Antimicrobial effects of silver nanoparticle-microspots on the mechanical properties of single bacteria
1
2024
1
10.1039/D4AN00174E
Analyst
149
2637-2646
G.
Caniglia
D.
Valavanis
G.
Tezcan
J.
Magiera
H.
Barth
J.
Bansmann
C.
Kranz
P. R.
Unwin
article
Assessing the Quality of Ionic Liquids Using Single Crystal Electrochemistry, Surface Science and Data Screening
2
2024
10.26434/chemrxiv-2024-zkknm
ChemRXIV
M.-K.
Heubach
J.
Bansmann
A. K.
Engstfeld
T.
Jacob
article
Borate modified Co-free LiNi0.5Mn1.5O4 cathode material: A pathway to superior interface and cycling stability in LNMO/graphite full-cells
2024
1
10.1016/j.cej.2024.152416
Chemical Engineering Journal
493
152416
U.
Nisar
J.
Bansmann
M.
Hebel
B.
Reichelt
M.
Mancini
M.
Wohlfahrt-Mehrens
M.
ö
P.
Axmann
article
Metal Alloy-Functionalized 3D-Printed Electrodes for Nitrate-to-Ammonia Conversion in Zinc-Nitrate Batteries
Electrocatalytic nitrate reduction is a promising approach to remove harmful nitrate and produce ammonia in aqueous media. Here, we demonstrate how 3D printed polymer electrodes can be electroless plated with a bimetallic NiCu alloy film suitable for sustained nitrate-to-ammonia reduction. Characterization by powder X-ray diffraction, X-ray photoelectron spectroscopy, scanning/transmission electron microscopy and energy-dispersive X-ray spectroscopy indicate that the electrode has a two-layer structure consisting of polymer/ coating layer of metal alloys. The composite electrode shows high-performance in the nitrate-to-ammonia electroreduction, giving NH3 Faradaic efficiencies of up to 83 % and NH3 yield rates up to 860 μg/(h cm2) at −0.38 V vs. RHE. We show that the electrode can easily be integrated into a Zn-nitrate battery, giving a power density of 3.8 mW cm−2 with continuous NH3 production. The system combines three productive outputs, that is removal of nitrate pollutants, synthesis of valuable ammonia and generation of “green” electricity.
2024
1
10.1002/celc.202400291
ChemElectroChem
11
e202400291
15
S.
Liu
Y.
Zhao
Z.
Chen
D.
Gao
F.
Feng
T.
Rios-Studer
J.
Bansmann
J.
Biskupek
U.
Kaiser
R.
Liu
Carsten
Streb
article
Selective Electroreduction of CO2 to Ethanol via Cobalt - Copper Tandem Catalysts
The selective electrocatalytic conversion of CO2 into multicarbon products, such as ethanol, is a major technological challenge. Currently, this reactivity is limited by the sluggish formation of C–C bonds inherent to many single-site catalysts. Here, we report a new tandem electrocatalyst based on earth-abundant elements, which facilitates the selective CO2-to-ethanol conversion. The composite catalyst consists of neighboring cobalt and copper atoms anchored to electrically conductive nitrogen-doped carbon. At low overpotentials (E = −0.8 V vs reversible hydrogen electrode), the system shows high selectivity for ethanol production (faradaic efficiencies {\textgreater}70\%), while retaining its reactivity and stability for 18 h. A CO spillover mechanism is proposed as the basis for the observed selectivity, where efficient CO generation at Co sites leads to high local CO concentrations at neighboring Cu sites, thereby favoring C–C coupling and ethanol formation. Operando X-ray absorption spectroscopy reveals a dynamic transformation of the single-site Cu into Cu clusters as actual active sites. In situ infrared spectroscopy reveals the formation of intermediate CO at Co sites, which undergo subsequent spillover and C–C coupling on the Cu clusters. This design concept offers new avenues for noble metal-free tandem electrocatalysts for the conversion of CO2-to-multicarbon products.
2024
1
10.1021/acscatal.4c05286
ACS Catalysis
14
15553-15564
20
S. A.
Chala
R.
Liu
E. O.
Oseghe
S. T.
Clausing
C.
Kampf
J.
Bansmann
A. H.
Clark
Y. K.
Zhou
I.
Lieberwirth
J.
Biskupek
U.
Kaiser
Carsten
Streb
article
Polymeric carbon nitride-based photocathodes for visible light-driven selective reduction of oxygen to hydrogen peroxide
2023
4
1
10.1016/j.apcata.2023.119173
Applied Catalysis A: General
660
119173
H.
Braun
D.
Mitoraj
A.
Hellmann
J.
Kuncewicz
M. M.
Elnagar
J.
Bansmann
C.
Kranz
T.
Jacob
W.
Macyk
R.
Beranek
article
Borate-Coated Co-Free LiNi 0.5 Mn 1.5 O 4 : Enhanced Performance and Stability for High-Power-Density Libs
2023
10.1149/MA2023-0283423mtgabs
The Electrochemical Society
MA2023-02
8
3423
U.
Nisar
J.
Bansmann
M.
Wohlfahrt-Mehrens
P.
Axmann
article
Icosahedral Gold Nanoparticles Decorated with Hexon Protein: A Surrogate for Adenovirus Serotype 5
The development of synthetic particles that emulate real viruses in size, shape, and chemical composition is vital to the development of imprinted polymer-based sorbent materials (MIPs). In this study, we address surrogates for adenovirus type 5 (Adv 5) via the synthesis and subsequent modification of icosahedral gold nanoparticles (iAuNPs) decorated with the most abundant protein of the Adv 5 (i.e., hexon protein) at the surface. CTAB-capped iAuNPs with dimensions between 40-90 nm were synthesized, and then CTAB was replaced by a variety of polyethylene glycols (PEGs) in order to introduce suitable functionalities serving as anchoring points for the attachment of hexon protein. The latter was achieved by non-covalent linking of the protein to the iAuNP surface using a PEG without reactive termination (i.e., methoxy PEG thiol, mPEG-SH, Mn=800). Alternatively, covalent anchoring points were generated by modifying the iAuNPs with a bifunctional PEG (i.e., thiol PEG amine, SH-PEG-NH2), followed by the addition of glutaraldehyde. X-ray photoelectron spectroscopy (XPS) confirmed the formation of the anchoring points at the iAuNP surface. Next, the amino groups present in the amino acids of hexon protein interacted with the glutaraldehyde. iAuNPs before and after PEGylation were characterized using dynamic light scattering (DLS), XPS, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and UV-vis spectroscopy, confirming the CTAB-PEG exchange. Finally, the distinct red-shift obtained in the UV-vis spectra of the pegylated iAuNPs in the presence of hexon protein, the increase of the hydrodynamic diameter, the change of the zeta potential as well as the selective binding of the hexon-modified iAuNPs towards a hexon-imprinted polymer (HIP), confirmed both the successful covalent and non-covalent attachment at the iAuNP surface.
2023
1
10.1007/s00216-022-04368-x
Analytical and Bioanalytical Chemistry
415
Springer Science and Business Media LLC
2080-2091
11
B.
Fresco-Cala
Ángela I.
ó-ǰԳٱ
A.
Batista
M.
Dinc
J.
Bansmann
R. J.
Behm
S.
Cárdenas Aranzana
B.
Mizaikoff
article
Unveiling the CO Oxidation Mechanism over a Molecularly- Defined Copper Single-Atom Catalyst Supported on a Metal- Organic Framework
2023
1
10.1002/anie.202301920
Angwandte Chemie International Edition
62
e202301920
30
A. M.
Abdel-Mageed
B.
Rungtaweevoranit
S.
Impeng
J.
Bansmann
J.
Rabeah
S.
Chen
T.
äԲ
S.
Namuangrak
K.
Faungnawakij
A.
üԱ
R. J.
Behm
article
A combined XPS and computational study of the chemical reduction of BMP-TFSI by lithium
Employing density functional theory (DFT) calculations and x-ray photoelectron spectroscopy (XPS), we identify products of the reaction of the ionic liquid N,N - butylmethylpyrrolidinum bis(triuoromethylsulfonyl)imide (BMP-TFSI) with lithium in order to model the initial chemical processes contributing to the formation of the solid electrolyte interphase in batteries. Besides lithium oxide, sulfide, carbide and fluoride, we find lithium cyanide or cyanamide as possible, thermodynamically stable products in the Li-poor regime, whilst Li$_{\textrm{3}}$N is the stable product in the Li-rich regime. The thermodynamically controlled reaction products as well as larger fragments of TFSI persisting due to kinetic barriers could be identified by a comparison of experimentally and computationally determined core level binding energies.
2022
1
10.1002/batt.202200307
Batteries & Supercaps
12
Wiley-VCH
Wiley
e202200307
5
K.
Forster-Tonigold
F.
Buchner
J.
Bansmann
R. J.
Behm
A.
Ұß
article
Atmospheric Pressure Plasma-Jet Treatment of PAN-Nonwovens: Carbonization of Nanofiber Electrodes
Carbon nanofibers are produced from dielectric polymer precursors such as polyacrylonitrile (PAN). Carbonized nanofiber nonwovens show high surface area and good electrical conductivity, rendering these fiber materials interesting for application as electrodes in batteries, fuel cells, and supercapacitors. However, thermal processing is slow and costly, which is why new processing techniques have been explored for carbon fiber tows. Alternatives for the conversion of PAN-precursors into carbon fiber nonwovens are scarce. Here, we utilize an atmospheric pressure plasma jet to conduct carbonization of stabilized PAN nanofiber nonwovens. We explore the influence of various processing parameters on the conductivity and degree of carbonization of the converted nanofiber material. The precursor fibers are converted by plasma-jet treatment to carbon fiber nonwovens within seconds, by which they develop a rough surface making subsequent surface activation processes obsolete. The resulting carbon nanofiber nonwovens are applied as supercapacitor electrodes and examined by cyclic voltammetry and impedance spectroscopy. Nonwovens that are carbonized within 60 s show capacitances of up to 5 F g−1
Journal Article
2022
1
10.3390/c8030033
C
8
33
3
A.
Hoffmann
M.
Uhl
M.
Ceblin
F.
Rohrbach
J.
Bansmann
M.
Mallah
H.
Heuermann
T.
Jacob
A. J. C.
Kuehne
article
Atmospheric pressure plasma-jet treatment of polyacrylonitrile-nonwovens:~Activation leading to high surface area carbon electrodes
Carbon nanofiber nonwovens (CFN) are powerful electrode materials withexceptional performance in energy storage devices, such as batteries andsupercapacitors. Small fiber‐diameters together with hierarchical porosity endowCFN‐electrode materials with large surface areas and high electrical capacitance.Porosity of the fiber surface is often realized by corrosive activation methods suchas wet‐etching or using oxidative gases at elevated temperatures. In this study, wepresent a chemical‐free, environmental‐friendly, and easily controllable surfaceactivation method using an atmospheric pressure plasma‐jet. We investigate thebest instant for activation along the process chain and show that the surface areaof nanofiber nonwovens can be tailored by adjusting the plasma exposure‐dose.Plasma‐activated CFNs showan almost 20‐fold increase incapacitance (CspPJ=10.1F/g)inan electrochemical supercapa-citor setup compared to non-activated CFN (CspnoPJ=0.55F/g).
2022
1
10.1002/ppap.202200114
Plasma Processes and Polymers
19
2200114
12
A.
Hoffmann
M.
Uhl
M.
Ceblin
J.
Bansmann
T.
Jacob
A. J. C.
Kuehne
article
Controlling the Selectivity of High-Surface-Area Ru/TiO2 Catalysts in CO2 Reduction - Modifying the Reaction Properties by Si Doping of the Support
Journal article
2022
1
10.1016/j.apcatb.2022.121748
Applied Catalysis B: Environmental
317
121748
S.
Cisneros
S.
Chen
C.
Fauth
A. M.
Abdel-Mageed
S.
Pollastri
J.
Bansmann
L.
Olivi
J.
Aquilanti
H.
Atia
J.
Rabeah
R. J.
Behm
article
Effect of Three-in-One Surface Modification of Spherical, Co-Free Li-Rich Cathode Material for Li-Ion Batteries (Li1.2Mn0.6Ni0.2O2) with Citric Acid
The electrochemical activation of Li2MnO3 domains in Li- and Mn-rich layered oxides (LRLO) is highly important, and can be tuned by surface modification of the active materials to improve their cycling performance. In this study, citric acid was employed as a combined organic acid, reducing agent, and carbon precursor in order to remove surface residues from the calcination process, implement an oxygen deficient layer on the surface of the primary LRLO particles, and cover their surface with a carbon-containing coating after a final annealing step. A broad selection of bulk and surface sensitive characterization methods was used to characterize the post-treated spherical particles, providing the evidence for successful creation of an oxygen deficient near-surface region, covered by carbon-containing deposits. Post-treated materials show enhanced electrochemical discharge capacities after progressive Li2MnO3 activation, reaching maximum capacities of 247 mAh g-1. Gassing measurements reveal the suppression of oxygen release during the first cycle, concomitant with an increased CO2 formation for the carbon-coated materials. The voltage profile analysis in combination with post-mortem characterization after 300 cycles provide insights into the aging of the treated materials, which underlines the importance of the relationship between structural changes during scalable post-treatment and the electrochemical performance of the powders.
2022
1
10.1149/1945-7111/acaa5c
Journal of The Electrochemical Society
169
120533
12
F.
Klein
C.
Pfeiffer
J.
Bansmann
Z.
Jusys
R. J.
Behm
M.
Wohlfahrt-Mehrens
Mika
Իé
P.
Axmann
article
Enhanced electrochemical capacity of spherical Co-free Li1.2Mn0.6Ni0.2O2 particles after a water and acid treatment and its influence on the initial gas evolution behavior
Journal article
2022
1
10.1002/cssc.202201061
ChemSusChem
15
e202201061
20
F.
Klein
J.
Bansmann
Z.
Jusys
C.
Pfeiffer
P.
Scheitenberger
M.
Mundszinger
D.
Geiger
J.
Biskupek
U.
Kaiser
R. J.
Behm
M.
Wohlfahrt-Mehrens
P.
Axmann
article
On-Chip Direct Laser Writing of PAN-Based Carbon Supercapacitor Electrodes
Journal Article
2022
https://doi.org/10.1002/marc.202100731
Macromolecular Rapid Communications
43
2100731
6
A.
Hoffmann
P.
Jimenez-Calvo
J.
Bansmann
V.
Strauss
A. J. C.
Kuehne
article
Reversible Growth of Gold Nanoparticles in the Low-Temperature Water−Gas Shift Reaction
Supported gold nanoparticles are widely studied catalysts and are among the most active known for the low-temperature water−gas shift reaction, which is essential in fuel and energy applications, but their practical application has been limited by their poor thermal stability. The catalysts deactivate on-stream via the growth of small Au nanoparticles. Using operando X-ray absorption and in situ scanning transmission electron microscopy, we report direct evidence that this process can be reversed by carrying out a facile oxidative treatment, which redisperses the gold nanoparticles and restores catalytic activity. The use of in situ methods reveals the complex dynamics of supported gold nanoparticles under reaction conditions and demonstrates that gold catalysts can be easily regenerated, expanding their scope for practical application.
2022
1
10.1021/acsnano.2c06504
ACS Nano
16
9
15197–15205
J. H.
Carter
A. M.
Abdel-Mageed
D.
Zhou
D. J.
Morgan
X.
Liu
J.
Bansmann
S.
Chen
R. J.
Behm
G.
Hutchings
article
Switchable Polyacrylonitrile-Copolymer for Melt-Processing and Thermal Carbonization - 3D Printing of Carbon Supercapacitor Electrodes with High Capacitance
Polyacrylonitrile (PAN) represents the most widely used precursor for carbon fibers and carbon materials. Carbon materials stand out with their high mechanical performance, but they also show excellent electrical conductivity and high surface area. These properties render carbon materials suitable as electrode material for fuel cells, batteries, and supercapacitors. However, PAN has to be processed from solution before being thermally converted to carbon, limiting its final format to fibers, films, and non-wovens. Here, we present a PAN-copolymer with an intrinsic plasticizer to reduce the melting temperature and avoid undesired entering of the thermal carbonization regime. This plasticizer enables melt extrusion-based additive manufacturing (EAM). The plasticizer in the PAN-copolymer can be switched to increase the melting temperature after processing, allowing the 3D-melt-printed workpiece to be thermally carbonized after EAM. Melt-processing of the PAN copolymer extends the freedom-in-design of carbon materials to mold-free rapid prototyping, in the absence of solvents, which enables more economic and sustainable manufacturing processes. As an example for the capability of this material system, we print open meshed carbon electrodes for supercapacitors that are metal- and binder-free with an optimized thickness of 1.5 mm and a capacitance of up to 387 mF cm-2 . This article is protected by copyright. All rights reserved.
2022
1
10.1002/adma.202208484
Advanced Materials
35
2208484
6
M.
Usselmann
J.
Bansmann
A. J. C.
Kuehne
article
Diemant_2021_COOxidation
CO Oxidation on Planar Au/TiO 2 Model Catalysts under Realistic Conditions: A Combined Kinetic and IR Study
Journal Article
2021
https://doi.org/10.1002/cphc.202000960
ChemPhysChem
22
542–552
6
J.
Bansmann
article
Cisneros_2021_EffectsOf
Effects of SiO2-doping on high-surface-area Ru/TiO_2 catalysts for the selective CO methanation
Journal Article
2021
https://doi.org/10.1016/j.apcatb.2020.119483
Appl. Catal., B
282
119483
S.
Cisneros
J.
Bansmann
A. M.
Abdel-Mageed
M.
Goepel
S. E.
Olesen
E. S.
Welter
M.
Parlinska-Wojtan
R.
ұä
I.
Chorkendorff
R. J.
Behm
article
Chen_2021_ElectronicMetal-Support
Electronic metal-support interactions and their promotional effect on CO2 methanation on Ru/ZrO2 catalysts
Journal Article
2021
https://doi.org/10.1016/j.jcat.2021.06.028
Journal of Catalysis
400
407-420
A. M.
Abdel-Mageed
S.
Cisneros
J.
Bansmann
J.
Rabeah
A.
üԱ
A.
Ұß
R. J.
Behm
article
Abdel-Mageed_2021_FundamentalAspectsOf
Fundamental Aspects of Ceria Supported Au Catalysts Probed by In Situ / Operando Spectroscopy and TAP Reactor Studies
Journal Article
2021
1
10.1002/cphc.202100027
ChemPhysChem
22
1302-1315
13
Operando Spectroscopy
Au/CeO2
XANES/EXAFS
DRIFTS
TAP Reactor
A. M.
Abdel-Mageed
C.
Fauth
T.
äԲ
J.
Bansmann
article
Schuettler_2021_InteractionOf
Interaction of bimetallic Zn/Au(111) surfaces with O2 or NO2 and formation of ZnOx/Au(111)
Journal Article
2021
10.1016/j.susc.2021.121863
Surface Science
711
121863
K. M.
üٳٱ
J.
Bansmann
A. K.
Engstfeld
R. J.
Behm
article
üٳٱ_2021_LowTemperatureNucleation
Low-temperature nucleation and growth of Zn on Au(111) and thermal stability toward (surface) alloy formation
Journal Article
2021
10.1063/5.0054980
The Journal of Chemical Physics
155
124704
12
K. M.
üٳٱ
J.
Bansmann
A. K.
Engstfeld
R. J.
Behm
article
Forster-Tonigold_2021_ModelStudies
Model Studies on the Formation of the Solid Electrolyte Interphase: Reaction of Li with Ultrathin Adsorbed Ionic-Liquid Films and Co 3 O 4 (111) Thin Films
Journal Article
2021
https://doi.org/10.1002/cphc.202001033
ChemPhysChem
22
441–454
5
K.
Forster-Tonigold
J.
Kim
J.
Bansmann
A.
Ұß
F.
Buchner
article
Engstfeld_2021_Ru
Ru(0001) surface electrochemistry in the presence of specifically adsorbing anions
Journal Article
2021
1
10.1016/j.electacta.2021.138350
Electrochimica Acta
389
138350
A. K.
Engstfeld
S.
Weizenegger
L.
Pithan
P.
Beyer
J.
Bansmann
R. J.
Behm
J.
Drnec
article
Abdel-Mageed-2021-SteeringTheSelectivity
Steering the selectivity in CO2 reduction on highly active Ru/TiO2 catalysts: Support particle size effects
Journal Article
2021
0.1016/j.jcat.2021.07.020
Journal of Catalysis
401
160-173
A. M.
Abdel-Mageed
K.
Wiese
A.
Hauble
J.
Bansmann
J.
Rabeah
M.
Parlinska-Wojtan
A.
üԱ
R. J.
Behm
article
Schuettler_2020_AdlayerGrowth
Adlayer growth vs spontaneous (near-) surface alloy formation: Zn growth on Au(111)
Journal Article
2020
https://doi.org/10.1063/1.5145294
J. Chem. Phys.
152
124701
12
K. M.
üٳٱ
J.
Bansmann
A. K.
Engstfeld
R. J.
Behm
article
Chen_2020_RaisingThe
Raising the COx Methanation Activity of a Ru/γ-Al2O3 Catalyst by Activated Modification of Metal–Support Interactions
Journal Article
2020
https://doi.org/10.1002/anie.202007228
Angew. Chem. - Int. Ed.
59
22763-22770
50
A. M.
Abdel-Mageed
M.
Dyballa
M.
Parlinska-Wojtan
J.
Bansmann
S.
Pollastri
L.
Olivi
G.
Aquilanti
R. J.
Behm
article
Bansmann_2019_ChemicalAnd
Chemical and Electronic Changes of the CeO2 Support during CO Oxidation on Au/CeO2 Catalysts: Time-Resolved Operando XAS at the Ce LIII Edge
Journal Article
2019
https://doi.org/10.3390/catal9100785
Catalysts
9
785
10
J.
Bansmann
A. M.
Abdel-Mageed
C.
Fauth
T.
äԲ
G.
Kucerova
R. J.
Behm
article
Buchner_2019_InteractionBetween
Interaction between Li, Ultrathin Adsorbed Ionic Liquid Films, and CoO(111) Thin Films: A Model Study of the Solid|Electrolyte Interphase Formation
Journal Article
2019
10.1021/acs.chemmater.9b01253
Chem. Mater.
31
5537-5549
15
F.
Buchner
K.
Forster-Tonigold
J.
Kim
J.
Bansmann
A.
Ұß
R. J.
Behm
article
Chen_2019_Morphology-EngineeredHighly
Morphology-Engineered Highly Active and Stable Ru/TiO2 Catalysts for Selective CO Methanation
Journal Article
2019
https://doi.org/10.1002/anie.201903882
Angewandte Chemie International Edition
58
10732-10736
31
A. M.
Abdel-Mageed
D.
Li
J.
Bansmann
S.
Cisneros
W.
Huang
R. J.
Behm
article
Buchner_2018_ExperimentalAnd
Experimental and Computational Study on the Interaction of an Ionic Liquid Monolayer with Lithium on Pristine and Lithiated Graphite
Journal Article
2018
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