TY  - JOUR
A1  - Herold, Heike M.
A1  - Aigner, Tamara Bernadette
A1  - Grill, Carolin E.
A1  - Krüger, Stefanie
A1  - Taubert, Andreas
A1  - Scheibel, Thomas R.
T1  - SpiderMAEn
BT  - recombinant spider silk-based hybrid materials for advanced energy technology
JF  - Bioinspired, Biomimetic and Nanobiomaterials
N2  - A growing energy demand requires new and preferably renewable energy sources. The infinite availability of solar radiation makes its conversion into storable and transportable energy forms attractive for research as well as for the industry. One promising example of a transportable fuel is hydrogen (H-2), making research into eco-friendly hydrogen production meaningful. Here, a hybrid system was developed using newly designed recombinant spider silk protein variants as a template for mineralization with inorganic titanium dioxide and gold. These bioinspired organic/inorganic hybrid materials allow for hydrogen production upon light irradiation. To begin with, recombinant spider silk proteins bearing titanium dioxide and gold-binding moieties were created and processed into structured films. These films were modified with gold and titanium dioxide in order to produce a photocatalyst. Subsequent testing revealed hydrogen production as a result of light-induced hydrolysis of water. Therefore, the novel setup presented here provides access to a new principle of generating advanced hybrid materials for sustainable hydrogen production and depicts a promising platform for further studies on photocatalytic production of hydrogen, the most promising future fuel.
KW  - hybrid materials
KW  - hydrogen
KW  - photocatalysts
Y1  - 2019
U6  - https://doi.org/10.1680/jbibn.18.00007
SN  - 2045-9858
SN  - 2045-9866
VL  - 8
IS  - 1
SP  - 99
EP  - 108
PB  - ICE Publishing
CY  - Westminister
ER  - 
TY  - JOUR
A1  - Unuabonah, Emmanuel Iyayi
A1  - Agunbiade, Foluso O.
A1  - Alfred, Moses O.
A1  - Adewumi, Thompson A.
A1  - Okoli, Chukwunonso P.
A1  - Omorogie, Martins O.
A1  - Akanbi, Moses O.
A1  - Ofomaja, Augustine E.
A1  - Taubert, Andreas
T1  - Facile synthesis of new amino-functionalized agrogenic hybrid composite clay adsorbents for phosphate capture and recovery from water
JF  - Journal of Cleaner Production
N2  - New hybrid clay materials with good affinity for phosphate ions were developed from a combination of biomass-Carica papaya seeds (PS) and Musa paradisiaca (Plantain peels-PP), ZnCl2 and Kaolinite clay to produce iPS-HYCA and iPP-HYCA composite adsorbents respectively. Functionalization of these adsorbents with an organosilane produced NPS-HYCA and NPP-HYCA composite adsorbents. The pH(pzc) for the adsorbents were 7.83, 6.91, 7.66 and 6.55 for iPS-HYCA, NPS-HYCA, iPP-HYCA and NPP-HYCA respectively. Using the Brouer-Sotolongo isotherm model which best predict the adsorption capacity of composites for phosphate, iPP-HYCA, iPS-HYCA, NPP-HYCA, and NPS-HYCA composite adsorbents respectively. When compared with some commercial resins, the amino-functionalized adsorbents had better adsorption capacities. Furthermore, amino-functionalized adsorbents showed improved adsorption capacity and rate of phosphate uptake (as much as 40-fold), as well as retain 94% (for NPS-HYCA) and 84.1% (for NPP-HYCA) efficiency for phosphate adsorption after 5 adsorption-desorption cycles (96 h of adsorption time with 100 mg/L of phosphate ions) as against 37.5% (for iPS-HYCA) and 35% (for iPP-HYCA) under similar conditions. In 25 min desorption of phosphate ion attained equilibrium. These new amino-functionalized hybrid clay composite adsorbents, which were prepared by a simple means that is sustainable, have potentials for the efficient capture of phosphate ions from aqueous solution. They are quickly recovered from aqueous solution, non-biodegradable (unlike many biosorbent) with potentials to replace expensive adsorbents in the future. They have the further advantage of being useful in the recovery of phosphate for use in agriculture which could positively impact the global food security programme. (C) 2017 Elsevier Ltd. All rights reserved.
KW  - Composite adsorbents
KW  - Sustainable
KW  - Phosphate recovery
KW  - Water
KW  - Desorption kinetics
Y1  - 2017
U6  - https://doi.org/10.1016/j.jclepro.2017.06.160
SN  - 0959-6526
SN  - 1879-1786
VL  - 164
SP  - 652
EP  - 663
PB  - Elsevier
CY  - Oxford
ER  - 
TY  - GEN
A1  - Ihlenburg, Ramona
A1  - Lehnen, Anne-Catherine
A1  - Koetz, Joachim
A1  - Taubert, Andreas
T1  - Sulfobetaine Cryogels for Preferential Adsorption of Methyl Orange from Mixed Dye Solutions
T2  - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
N2  - New cryogels for selective dye removal from aqueous solution were prepared by free radical polymerization from the highly water-soluble crosslinker N,N,N’,N’-tetramethyl-N,N’-bis(2-ethylmethacrylate)-propyl-1,3-diammonium dibromide and the sulfobetaine monomer 2-(N-3-sulfopropyl-N,N-dimethyl ammonium)ethyl methacrylate. The resulting white and opaque cryogels have micrometer sized pores with a smaller substructure. They adsorb methyl orange (MO) but not methylene blue (MB) from aqueous solution. Mixtures of MO and MB can be separated through selective adsorption of the MO to the cryogels while the MB remains in solution. The resulting cryogels are thus candidates for the removal of hazardous organic substances, as exemplified by MO and MB, from water. Clearly, it is possible that the cryogels are also potentially interesting for removal of other compounds such as pharmaceuticals or pesticides, but this must be investigated further.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1093 
KW  - cryogel
KW  - water treatment
KW  - dye removal
KW  - methyl orange
KW  - methylene blue
KW  - dye mixture
Y1  - 2021
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-488987
SN  - 1866-8372
IS  - 1093
ER  - 
TY  - JOUR
A1  - Ihlenburg, Ramona
A1  - Lehnen, Anne-Catherine
A1  - Koetz, Joachim
A1  - Taubert, Andreas
T1  - Sulfobetaine Cryogels for Preferential Adsorption of Methyl Orange from Mixed Dye Solutions
JF  - Polymers / Molecular Diversity Preservation International
N2  - New cryogels for selective dye removal from aqueous solution were prepared by free radical polymerization from the highly water-soluble crosslinker N,N,N’,N’-tetramethyl-N,N’-bis(2-ethylmethacrylate)-propyl-1,3-diammonium dibromide and the sulfobetaine monomer 2-(N-3-sulfopropyl-N,N-dimethyl ammonium)ethyl methacrylate. The resulting white and opaque cryogels have micrometer sized pores with a smaller substructure. They adsorb methyl orange (MO) but not methylene blue (MB) from aqueous solution. Mixtures of MO and MB can be separated through selective adsorption of the MO to the cryogels while the MB remains in solution. The resulting cryogels are thus candidates for the removal of hazardous organic substances, as exemplified by MO and MB, from water. Clearly, it is possible that the cryogels are also potentially interesting for removal of other compounds such as pharmaceuticals or pesticides, but this must be investigated further.
KW  - cryogel
KW  - water treatment
KW  - dye removal
KW  - methyl orange
KW  - methylene blue
KW  - dye mixture
Y1  - 2020
U6  - https://doi.org/10.3390/polym13020208
SN  - 2073-4360
VL  - 13
IS  - 2
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Ugwuja, Chidinma G.
A1  - Adelowo, Olawale O.
A1  - Ogunlaja, Aemere
A1  - Omorogie, Martins O.
A1  - Olukanni, Olumide D.
A1  - Ikhimiukor, Odion O.
A1  - Iermak, Ievgeniia
A1  - Kolawole, Gabriel A.
A1  - Günter, Christina
A1  - Taubert, Andreas
A1  - Bodede, Olusola
A1  - Moodley, Roshila
A1  - Inada, Natalia M.
A1  - Camargo, Andrea S.S. de
A1  - Unuabonah, Emmanuel Iyayi
T1  - Visible-Light-Mediated Photodynamic Water Disinfection @ Bimetallic-Doped Hybrid Clay Nanocomposites
JF  - ACS applied materials & interfaces
N2  - This study reports a new class of photocatalytic hybrid clay nanocomposites prepared from low-cost sources (kaolinite clay and Carica papaya seeds) doped with Zn and Cu salts via a solvothermal process. X-ray diffraction analysis suggests that Cu-doping and Cu/Zn-doping introduce new phases into the crystalline structure of Kaolinite clay, which is linked to the reduced band gap of kaolinite from typically between 4.9 and 8.2 eV to 2.69 eV for Cu-doped and 1.5 eV for Cu/Zn hybrid clay nanocomposites (Nisar, J.; Arhammar, C.; Jamstorp, E.; Ahuja, R. Phys. Rev. B 2011, 84, 075120). In the presence of solar light irradiation, Cu- and Cu/Zn-doped nanocomposites facilitate the electron hole pair separation. This promotes the generation of singlet oxygen which in turn improves the water disinfection efficiencies of these novel nanocomposite materials. The nanocomposite materials were further characterized using high-resolution scanning electron microscopy, fluorimetry, therrnogravimetric analysis, and Raman spectroscopy. The breakthrough times of the nanocomposites for a fixed bed mode of disinfection of water contaminated with 2.32 x 10(7) cfu/mL E. coli ATCC 25922 under solar light irradiation are 25 h for Zn-doped, 30 h for Cu-doped, and 35 h for Cu/Zn-doped nanocomposites. In the presence of multidrug and multimetal resistant strains of E. coli, the breakthrough time decreases significantly. Zn-only doped nanocomposites are not photocatalytically active. In the absence of light, the nanocomposites are still effective in decontaminating water, although less efficient than under solar light irradiation. Electrostatic interaction, metal toxicity, and release of singlet oxygen (only in the Cu-doped and Cu/Zn-doped nanocomposites) are the three disinfection mechanisms by which these nanocomposites disinfect water. A regrowth study indicates the absence of any living E. coli cells in treated water even after 4 days. These data and the long hydraulic times (under gravity) exhibited by these nanocomposites during photodisinfection of water indicate an unusually high potential of these nanocomposites as efficient, affordable, and sustainable point-of-use systems for the disinfection of water in developing countries.
KW  - disinfection
KW  - nanocomposite material
KW  - multidrug-resistant Escherichia coli
KW  - water
KW  - reactive oxygen species
Y1  - 2019
U6  - https://doi.org/10.1021/acsami.9b01212
SN  - 1944-8244
SN  - 1944-8252
VL  - 11
IS  - 28
SP  - 25483
EP  - 25494
PB  - American Chemical Society
CY  - Washington, DC
ER  - 
TY  - JOUR
A1  - Tao, Lumi
A1  - Liu, Yuchuan
A1  - Wu, Dan
A1  - Wei, Qiao-Hua
A1  - Taubert, Andreas
A1  - Xie, Zailai
T1  - Luminescent Ionogels with Excellent Transparency, High Mechanical Strength, and High Conductivity
JF  - Nanomaterials
N2  - The paper describes a new kind of ionogel with both good mechanical strength and high conductivity synthesized by confining the ionic liquid (IL) 1-butyl-3-methylimidazolium bis(trifluoromethane sulfonyl)imide ([Bmim][NTf₂]) within an organic–inorganic hybrid host. The organic–inorganic host network was synthesized by the reaction of methyltrimethoxysilane (MTMS), tetraethoxysilane (TEOS), and methyl methacrylate (MMA) in the presence of a coupling agent, offering the good mechanical strength and rapid shape recovery of the final products. The silane coupling agent 3-methacryloxypropyltrimethoxysilane (KH-570) plays an important role in improving the mechanical strength of the inorganic–organic hybrid, because it covalently connected the organic component MMA and the inorganic component SiO₂. Both the thermal stability and mechanical strength of the ionogel significantly increased by the addition of IL. The immobilization of [Bmim][NTf₂] within the ionogel provided the final ionogel with an ionic conductivity as high as ca. 0.04 S cm⁻¹ at 50 °C. Moreover, the hybrid ionogel can be modified with organosilica-modified carbon dots within the network to yield a transparent and flexible ionogel with strong excitation-dependent emission between 400 and 800 nm. The approach is, therefore, a blueprint for the construction of next-generation multifunctional ionogels.
KW  - ionic liquid
KW  - ionogel
KW  - carbon dots
KW  - organic–inorganic hybrid
KW  - luminescence
KW  - mechanical strength
Y1  - 2020
U6  - https://doi.org/10.3390/nano10122521
SN  - 2079-4991
VL  - 10
IS  - 12
PB  - MDPI
CY  - Basel
ER  - 
TY  - GEN
A1  - Tao, Lumi
A1  - Liu, Yuchuan
A1  - Wu, Dan
A1  - Wei, Qiao-Hua
A1  - Taubert, Andreas
A1  - Xie, Zailai
T1  - Luminescent Ionogels with Excellent Transparency, High Mechanical Strength, and High Conductivity
T2  - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
N2  - The paper describes a new kind of ionogel with both good mechanical strength and high conductivity synthesized by confining the ionic liquid (IL) 1-butyl-3-methylimidazolium bis(trifluoromethane sulfonyl)imide ([Bmim][NTf₂]) within an organic–inorganic hybrid host. The organic–inorganic host network was synthesized by the reaction of methyltrimethoxysilane (MTMS), tetraethoxysilane (TEOS), and methyl methacrylate (MMA) in the presence of a coupling agent, offering the good mechanical strength and rapid shape recovery of the final products. The silane coupling agent 3-methacryloxypropyltrimethoxysilane (KH-570) plays an important role in improving the mechanical strength of the inorganic–organic hybrid, because it covalently connected the organic component MMA and the inorganic component SiO₂. Both the thermal stability and mechanical strength of the ionogel significantly increased by the addition of IL. The immobilization of [Bmim][NTf₂] within the ionogel provided the final ionogel with an ionic conductivity as high as ca. 0.04 S cm⁻¹ at 50 °C. Moreover, the hybrid ionogel can be modified with organosilica-modified carbon dots within the network to yield a transparent and flexible ionogel with strong excitation-dependent emission between 400 and 800 nm. The approach is, therefore, a blueprint for the construction of next-generation multifunctional ionogels.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1058 
KW  - ionic liquid
KW  - ionogel
KW  - carbon dots
KW  - organic–inorganic hybrid
KW  - luminescence
KW  - mechanical strength
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-487334
SN  - 1866-8372
IS  - 1058
ER  - 
TY  - GEN
A1  - Schneider, Matthias
A1  - Günter, Christina
A1  - Taubert, Andreas
T1  - Co-deposition of a hydrogel/calcium phosphate hybrid layer on 3D printed poly(lactic acid) scaffolds via dip coating
BT  - Towards automated biomaterials fabrication
T2  - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
N2  - The article describes the surface modification of 3D printed poly(lactic acid) (PLA) scaffolds with calcium phosphate (CP)/gelatin and CP/chitosan hybrid coating layers. The presence of gelatin or chitosan significantly enhances CP co-deposition and adhesion of the mineral layer on the PLA scaffolds. The hydrogel/CP coating layers are fairly thick and the mineral is a mixture of brushite, octacalcium phosphate, and hydroxyapatite. Mineral formation is uniform throughout the printed architectures and all steps (printing, hydrogel deposition, and mineralization) are in principle amenable to automatization. Overall, the process reported here therefore has a high application potential for the controlled synthesis of biomimetic coatings on polymeric biomaterials.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1057 
KW  - 3D printing
KW  - dip-coating
KW  - poly(lactic acid)
KW  - PLA
KW  - calcium phosphate
KW  - gelatin
KW  - chitosan
KW  - hydrogel
KW  - calcium phosphate hybrid material
KW  - biomaterials
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-474427
SN  - 1866-8372
IS  - 1057
ER  - 
TY  - GEN
A1  - Vioux, André
A1  - Taubert, Andreas
T1  - Ionic liquids 2014 and selected papers from ILMAT 2013
BT  - Highlighting the ever-growing potential of Ionic Liquids
T2  - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1055 
KW  - electrolytes
KW  - extraction
KW  - system
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-475062
SN  - 1866-8372
IS  - 1055
ER  - 
TY  - GEN
A1  - Heyne, Benjamin
A1  - Arlt, Kristin
A1  - Geßner, André
A1  - Richter, Alexander F.
A1  - Döblinger, Markus
A1  - Feldmann, Jochen
A1  - Taubert, Andreas
A1  - Wedel, Armin
T1  - Mixed Mercaptocarboxylic Acid Shells Provide Stable Dispersions of InPZnS/ZnSe/ZnS Multishell Quantum Dots in Aqueous Media
T2  - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
N2  - Highly luminescent indium phosphide zinc sulfide (InPZnS) quantum dots (QDs), with zinc selenide/zinc sulfide (ZnSe/ZnS) shells, were synthesized. The QDs were modified via a post-synthetic ligand exchange reaction with 3-mercaptopropionic acid (MPA) and 11-mercaptoundecanoic acid (MUA) in different MPA:MUA ratios, making this study the first investigation into the effects of mixed ligand shells on InPZnS QDs. Moreover, this article also describes an optimized method for the correlation of the QD size vs. optical absorption of the QDs. Upon ligand exchange, the QDs can be dispersed in water. Longer ligands (MUA) provide more stable dispersions than short-chain ligands. Thicker ZnSe/ZnS shells provide a better photoluminescence quantum yield (PLQY) and higher emission stability upon ligand exchange. Both the ligand exchange and the optical properties are highly reproducible between different QD batches. Before dialysis, QDs with a ZnS shell thickness of ~4.9 monolayers (ML), stabilized with a mixed MPA:MUA (mixing ratio of 1:10), showed the highest PLQY, at ~45%. After dialysis, QDs with a ZnS shell thickness of ~4.9 ML, stabilized with a mixed MPA:MUA and a ratio of 1:10 and 1:100, showed the highest PLQYs, of ~41%. The dispersions were stable up to 44 days at ambient conditions and in the dark. After 44 days, QDs with a ZnS shell thickness of ~4.9 ML, stabilized with only MUA, showed the highest PLQY, of ~34%.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1026 
KW  - quantum dots
KW  - cadmium-free
KW  - Cd-free
KW  - InP
KW  - InPZnS
KW  - multishell
KW  - mercaptocarboxylic acids
KW  - 3-mercaptopropionic acid
KW  - 11-mercaptoundecanoic acid
KW  - phase transfer
KW  - ligand exchange
KW  - aqueous dispersion
KW  - QDs
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-486032
SN  - 1866-8372
IS  - 1026
ER  - 
TY  - JOUR
A1  - Heyne, Benjamin
A1  - Arlt, Kristin
A1  - Geßner, André
A1  - Richter, Alexander F.
A1  - Döblinger, Markus
A1  - Feldmann, Jochen
A1  - Taubert, Andreas
A1  - Wedel, Armin
T1  - Mixed Mercaptocarboxylic Acid Shells Provide Stable Dispersions of InPZnS/ZnSe/ZnS Multishell Quantum Dots in Aqueous Media
JF  - Nanomaterials
N2  - Highly luminescent indium phosphide zinc sulfide (InPZnS) quantum dots (QDs), with zinc selenide/zinc sulfide (ZnSe/ZnS) shells, were synthesized. The QDs were modified via a post-synthetic ligand exchange reaction with 3-mercaptopropionic acid (MPA) and 11-mercaptoundecanoic acid (MUA) in different MPA:MUA ratios, making this study the first investigation into the effects of mixed ligand shells on InPZnS QDs. Moreover, this article also describes an optimized method for the correlation of the QD size vs. optical absorption of the QDs. Upon ligand exchange, the QDs can be dispersed in water. Longer ligands (MUA) provide more stable dispersions than short-chain ligands. Thicker ZnSe/ZnS shells provide a better photoluminescence quantum yield (PLQY) and higher emission stability upon ligand exchange. Both the ligand exchange and the optical properties are highly reproducible between different QD batches. Before dialysis, QDs with a ZnS shell thickness of ~4.9 monolayers (ML), stabilized with a mixed MPA:MUA (mixing ratio of 1:10), showed the highest PLQY, at ~45%. After dialysis, QDs with a ZnS shell thickness of ~4.9 ML, stabilized with a mixed MPA:MUA and a ratio of 1:10 and 1:100, showed the highest PLQYs, of ~41%. The dispersions were stable up to 44 days at ambient conditions and in the dark. After 44 days, QDs with a ZnS shell thickness of ~4.9 ML, stabilized with only MUA, showed the highest PLQY, of ~34%.
KW  - quantum dots
KW  - cadmium-free
KW  - Cd-free
KW  - InP
KW  - InPZnS
KW  - multishell
KW  - mercaptocarboxylic acids
KW  - 3-mercaptopropionic acid
KW  - 11-mercaptoundecanoic acid
KW  - phase transfer
KW  - ligand exchange
KW  - aqueous dispersion
KW  - QDs
Y1  - 2020
U6  - https://doi.org/10.3390/nano10091858
SN  - 2079-4991
VL  - 10
IS  - 9
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Zehbe, Kerstin
A1  - Lange, Alyna
A1  - Taubert, Andreas
T1  - Stereolithography Provides Access to 3D Printed lonogels with High Ionic Conductivity
JF  - Energy Fuels
N2  - New ionogels (IGs) were prepared by combination of a series of sulfonate-based ionic liquids (ILs), 1-methyl-3-(4-sulfobutyl)imidazolium para-toluenesulfonate [BmimSO(3)][pTS], 1-methyl-1-butylpiperidiniumsulfonate para-toluenesul-fonate [BmpipSO(3)] [pTS], and 1-methyl-3-(4-sulfobutyl) imidazolium methylsulfonate [BmimSO(3)H][MeSO3] with a commercial stereolithography photoreactive resin. The article describes both the fundamental properties of the ILs and the resulting IGs. The IGs obtained from the ILs and the resin show high ionic conductivity of up to ca. 0.7.10(-4) S/cm at room temperature and 3.4-10(-3) S/cm at 90 degrees C. Moreover, the IGs are thermally stable to about 200 degrees C and mechanically robust. Finally, and most importantly, the article demonstrates that the IGs can be molded three-dimensionally using stereolithography. This provides, for the first time, access to IGs with complex 3D shapes with potential application in battery or fuel cell technology.
Y1  - 2019
U6  - https://doi.org/10.1021/acs.energyfuels.9b03379
SN  - 0887-0624
SN  - 1520-5029
VL  - 33
IS  - 12
SP  - 12885
EP  - 12893
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Taubert, Andreas
A1  - Leroux, Fabrice
A1  - Rabu, Pierre
A1  - de Zea Bermudez, Veronica
T1  - Advanced hybrid nanomaterials
JF  - Beilstein journal of nanotechnology
KW  - colloidal chemistry
KW  - environmental remediation
KW  - hybrid nanomaterials
KW  - nanocomposite
KW  - nanofillers
KW  - nanomedicine
KW  - nanostructures
KW  - polymer fillers
KW  - pore templating
KW  - smart materials
Y1  - 2019
U6  - https://doi.org/10.3762/bjnano.10.247
SN  - 2190-4286
VL  - 10
SP  - 2563
EP  - 2567
PB  - Beilstein-Institut zur Förderung der Chemischen Wissenschaften
CY  - Frankfurt am Main
ER  - 
TY  - JOUR
A1  - Peh, Eddie
A1  - Liedel, Clemens
A1  - Taubert, Andreas
A1  - Tauer, Klaus
T1  - Composition inversion to form calcium carbonate mixtures
JF  - CrystEngComm
N2  - Composition inversion takes place in equimolar solid mixtures of sodium or ammonium carbonate and calcium chloride with respect to the combination of anions and cations leading to the corresponding chloride and calcite in complete conversion. The transformation takes place spontaneously under a variety of different situations, even in a powdery mixture resting under ambient conditions. Powder X-ray diffraction data and scanning electron microscopy micrographs are presented to describe the course of the reaction and to characterize the reaction products. The incomplete reaction in the interspace between two compressed tablets of pure starting materials leads to an electric potential due to the presence of uncompensated charges.
Y1  - 2017
U6  - https://doi.org/10.1039/c7ce00433h
SN  - 1466-8033
VL  - 19
SP  - 3573
EP  - 3583
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Zhang, Weiyi
A1  - Willa, Christoph
A1  - Sun, Jian-Ke
A1  - Guterman, Ryan
A1  - Taubert, Andreas
A1  - Yuan, Jiayin
T1  - Polytriazolium poly(ionic liquid) bearing triiodide anions: Synthesis, basic properties and electrochemical behaviors
JF  - Polymer : the international journal for the science and technology of polymers
N2  - 4-Methyl-1-vinyl-1,2,4-triazolium triiodide ionic liquid and its polymer poly(4-methyl-1-vinyl-1,2,4-triazolium) triiodide were prepared for the first time from their iodide precursors via the reaction of iodide (I-) with elemental iodine (I-2). The change from iodide to triiodide (I-3(-)) was found to introduce particular variations in the physical properties of these two compounds, including lower melting point/glass transition temperature and altered solubility. The compounds were characterized by single-crystal X-ray diffraction, elemental analysis, and their electrochemical properties examined in solution and in the solid-state. Compared with their iodide analogues, the triiodide salts exhibited lower electrical impedance and higher current in the cyclic voltammetry. We found that poly(4-methyl-1,2,4-triazolium triiodide) was proven to be a promising solid polymer electrolyte candidate. (C) 2017 Elsevier Ltd. All rights reserved.
KW  - Poly(ionic liquid)
KW  - Solid polymer electrolyte
KW  - Grotthuss mechanism
KW  - Triiodide "network"
Y1  - 2017
U6  - https://doi.org/10.1016/j.polymer.2017.07.059
SN  - 0032-3861
SN  - 1873-2291
VL  - 124
SP  - 246
EP  - 251
PB  - Elsevier
CY  - Oxford
ER  - 
TY  - JOUR
A1  - Hentrich, Doreen
A1  - Brezesinski, Gerald
A1  - Kuebel, Christian
A1  - Bruns, Michael
A1  - Taubert, Andreas
T1  - Cholesteryl Hemisuccinate Monolayers Efficiently Control Calcium Phosphate Nucleation and Growth
JF  - Crystal growth & design : integrating the fields of crystal engineering and crystal growth for the synthesis and applications of new materials
N2  - The article describes the phase behavior of cholesteryl hemisuccinate at the air-liquid interface and its effect on calcium phosphate (CP) mineralization. The amphiphile forms stable monolayers with phase transitions at the air-liquid interface from a gas to a tilted liquid-condensed (TLC) and finally to an untilted liquid-condensed (ULC) phase. CP mineralization beneath these monolayers leads to crumpled CP layers made from individual plates. The main crystal phase is octacalcium phosphate (OCP) along with a minor fraction of hydroxyapatite (HAP), as confirmed by X-ray photoelectron spectroscopy, energy dispersive X-ray spectroscopy, bright field transmission electron microscopy, and electron diffraction.
Y1  - 2017
U6  - https://doi.org/10.1021/acs.cgd.7b00753
SN  - 1528-7483
SN  - 1528-7505
VL  - 17
SP  - 5764
EP  - 5774
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Abouserie, Ahed
A1  - Zehbe, Kerstin
A1  - Metzner, Philipp
A1  - Kelling, Alexandra
A1  - Günter, Christina
A1  - Schilde, Uwe
A1  - Strauch, Peter
A1  - Körzdörfer, Thomas
A1  - Taubert, Andreas
T1  - Alkylpyridinium Tetrahalidometallate Ionic Liquids and Ionic Liquid Crystals: Insights into the Origin of Their Phase Behavior
JF  - European journal of inorganic chemistry : a journal of ChemPubSoc Europe
N2  - Six N-alkylpyridinium salts [CnPy](2)[MCl4] (n = 4 or 12 and M = Co, Cu, Zn) were synthesized, and their structure and thermal properties were studied. The [C4Py](2)[MCl4] compounds are monoclinic and crystallize in the space group P2(1)/n. The crystals of the longer chain analogues [C12Py](2)[MCl4] are triclinic and crystallize in the space group P (1) over bar. Above the melting temperature, all compounds are ionic liquids (ILs). The derivatives with the longer C12 chain exhibit liquid crystallinity and the shorter chain compounds only show a melting transition. Consistent with single-crystal analysis, electron paramagnetic resonance spectroscopy suggests that the [CuCl4](2-) ions in the Cu-based ILs have a distorted tetrahedral geometry.
KW  - Ionic liquids
KW  - Alkylpyridinium salts
KW  - Structure elucidation
KW  - Phase transitions
Y1  - 2017
U6  - https://doi.org/10.1002/ejic.201700826
SN  - 1434-1948
SN  - 1099-0682
SP  - 5640
EP  - 5649
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Abouserie, Ahed
A1  - Zehbe, Kerstin
A1  - Metzner, Philipp
A1  - Kelling, Alexandra
A1  - Günter, Christina
A1  - Schilde, Uwe
A1  - Strauch, Peter
A1  - Körzdörfer, Thomas
A1  - Taubert, Andreas
T1  - Alkylpyridinium Tetrahalidometallate Ionic Liquids and Ionic Liquid Crystals: Insights into the Origin of Their Phase Behavior
JF  - European journal of inorganic chemistry : a journal of ChemPubSoc Europe
N2  - Six N-alkylpyridinium salts [CnPy](2)[MCl4] (n = 4 or 12 and M = Co, Cu, Zn) were synthesized, and their structure and thermal properties were studied. The [C4Py](2)[MCl4] compounds are monoclinic and crystallize in the space group P2(1)/n. The crystals of the longer chain analogues [C12Py](2)[MCl4] are triclinic and crystallize in the space group P (1) over bar. Above the melting temperature, all compounds are ionic liquids (ILs). The derivatives with the longer C12 chain exhibit liquid crystallinity and the shorter chain compounds only show a melting transition. Consistent with single-crystal analysis, electron paramagnetic resonance spectroscopy suggests that the [CuCl4](2-) ions in the Cu-based ILs have a distorted tetrahedral geometry.
KW  - Ionic liquids
KW  - Alkylpyridinium salts
KW  - Structure elucidation
KW  - Phase transitions
Y1  - 2017
U6  - https://doi.org/10.1002/ejic.201700826
SN  - 1434-1948
SN  - 1099-0682
SP  - 5640
EP  - 5649
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Göbel, Ronald
A1  - Stoltenberg, Marcus
A1  - Krehl, Stefan
A1  - Biolley, Christine
A1  - Rothe, Regina
A1  - Schmidt, Bernd
A1  - Hesemann, Peter
A1  - Taubert, Andreas
T1  - A Modular Approach towards Mesoporous Silica Monoliths with Organically Modified Pore Walls: Nucleophilic Addition, Olefin Metathesis, and Cycloaddition
JF  - European journal of inorganic chemistry : a journal of ChemPubSoc Europe
N2  - We have synthesized mesoporous silica (monoliths) with defined surface chemistry by means of a number of addition reactions: (i) coupling of an isocyanate to a surface-immobilized thiol, (ii) addition of an epoxide to a surface-immobilized thiol, (iii) cross-metathesis between two olefins, and (iv) Huisgen [2+3] cycloaddition of an alkyne-functionalized silica monolith with an azide. Functionalization of the mesopores was observed, but there are significant differences between individual approaches. Isocyanate and epoxide additions lead to high degrees of functionalization, whereas olefin metathesis and [2+3] cycloaddition are less effective. We further show that the efficiency of the modification is about twice as high in mesoporous silica particles than in macroscopic silica monoliths.
KW  - Mesoporous materials
KW  - Hybrid materials
KW  - Surface chemistry
KW  - Click chemistry
KW  - Nucleophilic addition
Y1  - 2016
U6  - https://doi.org/10.1002/ejic.201500638
SN  - 1434-1948
SN  - 1099-0682
VL  - 6
SP  - 2088
EP  - 2099
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - GEN
A1  - Zehbe, Kerstin
A1  - Kollosche, Matthias
A1  - Lardong, Sebastian
A1  - Kelling, Alexandra
A1  - Schilde, Uwe
A1  - Taubert, Andreas
T1  - Ionogels based on poly(methyl methacrylate) and metal-containing ionic liquids
BT  - correlation between structure and mechanical and electrical properties
N2  - Ionogels (IGs) based on poly(methyl methacrylate) (PMMA) and the metal-containing ionic liquids (ILs) bis-1-butyl-3-methlimidazolium tetrachloridocuprate(II), tetrachloride cobaltate(II), and tetrachlorido manganate(II) have been synthesized and their mechanical and electrical properties have been correlated with their microstructure. Unlike many previous examples, the current IGs show a decreasing stability in stress-strain experiments on increasing IL fractions. The conductivities of the current IGs are lower than those observed in similar examples in the literature. Both effects are caused by a two-phase structure with micrometer-sized IL-rich domains homogeneously dispersed an IL-deficient continuous PMMA phase. This study demonstrates that the IL-polymer miscibility and the morphology of the IGs are key parameters to control the (macroscopic) properties of IGs.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 361 
KW  - microstructure
KW  - ionogels
KW  - ionic liquids
KW  - phase separation
KW  - mechanical properties
KW  - ionic conductivity
Y1  - 2017
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-400607
ER  -