63077
2022
2022
eng
17
18
article
Elsevier
Amsterdam
1
2022-06-01
2022-06-01
--
Advances in characteristics improvement of polymeric membranes/separators for zinc-air batteries
Zinc-air batteries (ZABs) are gaining popularity for a wide range of applications due to their high energy density, excellent safety, and environmental friendliness. A membrane/separator is a critical component of ZABs, with substantial implications for battery performance and stability, particularly in the case of a battery in solid state format, which has captured increased attention in recent years. In this review, recent advances as well as insight into the architecture of polymeric membrane/separators for ZABs including porous polymer separators (PPSs), gel polymer electrolytes (GPEs), solid polymer electrolytes (SPEs) and anion exchange membranes (AEMs) are discussed. The paper puts forward strategies to enhance stability, ionic conductivity, ionic selectivity, electrolyte storage capacity and mechanical properties for each type of polymeric membrane. In addition, the remaining major obstacles as well as the most potential avenues for future research are examined in detail.
Materials Today Sustainability
10.1016/j.mtsust.2022.100126
2589-2347
outputup:dataSource:WoS:2022
100126
WOS:000832975000006
Kheawhom, S (corresponding author), Chulalongkorn Univ, Fac Engn, Dept Chem Engn, Bangkok 10330, Thailand.; Lu, Y (corresponding author), Helmholtz Zentrum Berlin Mat & Energie, Dept Electrochem Energy Storage, Hahn Meitner Pl 1, Berlin, Germany.; Kheawhom, S (corresponding author), Chulalongkorn Univ, Res Unit Adv Mat Energy Storage, Bangkok 10330, Thailand.; Kheawhom, S (corresponding author), Chulalongkorn Univ, Biocircular Green Econ Technol & Engn Ctr BCGeTEC, Fac Engn, Bangkok 10330, Thailand.; Lu, Y (corresponding author), Univ Potsdam, Inst Chem, Potsdam, Germany., soorathep.k@chula.ac.th; yan.lu@helmholtz-berlin.de
Program Unit for Human Resources & Institutional Development, Research; and Innovation [B16F640166]; National Science and Technology Development; Agency [P-20-50281]; Energy Storage Cluster, Chulalongkorn University;; Chulalongkorn Academic Advancement into its 2nd Century Project for; Postdoctoral Fellowship
Lu, Yan
2024-03-27T12:15:29+00:00
sword
importub
filename=package.tar
c4352f9538c25cf7f0155bb0871fbcd8
false
true
Ali Abbasi
Yaolin Xu
Ramin Khezri
Mohammad Etesami
C. Lin
Soorathep Kheawhom
Yan Lu
eng
uncontrolled
Ionic selectivity
eng
uncontrolled
Ionic conductivity
eng
uncontrolled
Gel polymer
eng
uncontrolled
Ion exchange
eng
uncontrolled
Porous
eng
uncontrolled
polymer
Chemie und zugeordnete Wissenschaften
Institut für Chemie
Referiert
Import
63027
2022
eng
9
558
article
Elsevier
Amsterdam
1
2022-03-09
2022-06-01
--
Experimental and theoretical gas-phase absorption spectra of thionated uracils
We present a comparative study of the gas-phase UV spectra of uracil and its thionated counterparts (2-thiouracil, 4-thiouracil and 2,4-dithiouracil), closely supported by time-dependent density functional theory calculations to assign the transitions observed. We systematically discuss pure gas-phase spectra for the (thio)uracils in the range of 200-400 nm (similar to 3.2-6.4 eV), and examine the spectra of all four species with a single theoretical approach. We note that specific vibrational modelling is needed to accurately determine the spectra across the examined wavelength range, and systematically model the transitions that appear at wavelengths shorter than 250 nm. Additionally, we find in the cases of 2-thiouracil and 2,4-dithiouracil, that the gas-phase spectra deviate significantly from some previously published solution-phase spectra, especially those collected in basic environments.
Chemical physics : a journal devoted to experimental and theoretical research involving problems of both a chemical and physical nature
10.1016/j.chemphys.2022.111500
0301-0104
outputup:dataSource:WoS:2022
111500
WOS:000792916900001
Robinson, Matthew S. (corresponding author), Deutsch Elektronen Synchrotron DESY, Ctr Free Electron Laser Sci CFEL, Notkestr 85, D-22607 Hamburg, Germany., matthew.robinson@cfel.de
Volkswagen foundation; DFG [GU 1478/1-1]
Robinson, Matthew S.
2024-03-21T07:51:03+00:00
sword
importub
filename=package.tar
306a40a65134699ecf8f459fec5a0f97
false
true
Dennis Mayer
David Picconi
Matthew S. Robinson
Markus Gühr
eng
uncontrolled
Thiouracil
eng
uncontrolled
Uracil
eng
uncontrolled
UV-VIS Spectroscopy
eng
uncontrolled
Excited-state calculations;
eng
uncontrolled
TD-DFT
eng
uncontrolled
Gas phase
Physik
Chemie und zugeordnete Wissenschaften
Institut für Physik und Astronomie
Institut für Chemie
Referiert
Import
60903
2020
2020
eng
28
39
12
1-2
91
article
Sage Publ.
London
1
2020-06-17
2020-06-17
--
Organic dye anchor peptide conjugates as an advanced coloring agent for polypropylene yarn
Polypropylene as one of the world's top commodity polymers is also widely used in the textile industry. However, its non-polar nature and partially crystalline structure significantly complicate the process of industrial coloring of polypropylene. Currently, textiles made of polypropylene or with a significant proportion of polypropylene are dyed under quite harsh conditions, including the use of high pressures and temperatures, which makes this process energy intensive. This research presents a three-step synthesis of coloring agents, capable of adhering onto synthetic polypropylene yarns without harsh energy-consuming conditions. This is possible by encapsulation of organic pigments using trimethoxyphenylsilane, introduction of surface double bonds via modification of the silica shell with trimethoxysilylpropylmethacrylate and final attachment of highly adhesive anchor peptides using thiol-ene chemistry. We demonstrate the applicability of this approach by dyeing polypropylene yarns in a simple process under ambient conditions after giving a step-by-step guide for the synthesis of these new dyeing agents. Finally, the successful dyeing of the yarns is visualized, and its practicability is discussed.
Textile Research Journal
10.1177/0040517520932231
0040-5175
1746-7748
outputup:dataSource:WoS:2021
0040517520932231
WOS:000542361500001
Boker, A (corresponding author), Fraunhofer Inst Appl Polymer Res IAP, Geiselbergstr 69, D-14476 Potsdam, Germany., alexander.boeker@iap.fraunhofer.de
Böker, Alexander
2023-09-25T05:54:49+00:00
sword
importub
filename=package.tar
5e5fef44c8af7848a50fe85bfe56e290
2209596-2
160931-2
<a href="https://doi.org/10.25932/publishup-54891">Zweitveröffentlichung in der Schriftenreihe Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe ; 1380</a>
false
false
CC-BY-NC - Namensnennung, nicht kommerziell 4.0 International
Marc Zimmermann
Benjamin René Harald Stomps
Christine Schulte-Osseili
Dmitry Grigoriev
Dirk Ewen
Andrew Morgan
Alexander Böker
eng
uncontrolled
anchor peptides
eng
uncontrolled
organic dye pigments
eng
uncontrolled
coloring agents
eng
uncontrolled
polypropylene
eng
uncontrolled
yarns
Chemie und zugeordnete Wissenschaften
Institut für Chemie
Referiert
Import
Hybrid Open-Access
62962
2022
2022
eng
55
63
9
186
article
Elsevier Science
Amsterdam [u.a.]
1
2021-10-01
2022-10-01
--
Changes of porosity of hard carbons during mechanical treatment and the relevance for sodium-ion anodes
Lithium-ion batteries have revolutionized battery technology. However, the scarcity of lithium in nature is driving the search for alternatives. For that reason, sodium-ion batteries have attracted increasing attention in recent years. The main obstacle to their development is the anode as, unlike for lithium-ion batteries, graphite cannot be used due to the inability to form stoichiometrically useful intercalation compounds with sodium. A promising candidate for sodium storage is hard carbon a form of nongraphitisable carbon, that can be synthesized from various precursor materials. Processing of hard carbons is often done by using mechanochemical treatments. Although it is generally accepted and often observed that they can influence the porosity of hard carbons, their effect on battery performance not well understood. Here, the changes in porosity occurring during ball milling are elucidated and related to the properties of hard carbons in sodium storage. Analysis by combined gas physisorption and small angle X-ray scattering shows that porosity changes during ball milling with a significant increase of the open porosity, unsuitable for reversible sodium storage, and decrease of the closed porosity, suitable for reversible sodium storage. While pristine hard carbon can store 58.5 mAh g(-1) in the closed pores, upon 5 h of mechanical treatment in a ball mill it can only store 35.5 mAh g(-1). The obtained results are furthermore pointing towards the disputed "intercalation-adsorption" mechanism.
Carbon : an international journal sponsored by the American Carbon Society
10.1016/j.carbon.2021.09.063
0008-6223
1873-3891
outputup:dataSource:WoS:2022
WOS:000708738000007
Ilic, Ivan (corresponding author), Univ Potsdam, Inst Chem, Karl Liebknecht Str 24-25, D-14476 Potsdam, Germany.; Oschatz, M (corresponding author), Friedrich Schiller Univ Jena, Ctr Energy & Environm Chem Jena CEEC Jena, Inst Tech Chem & Environm Chem, Philosophenweg 7a, D-07743 Jena, Germany., ivilic@uni-potsdam.de; martin.oschatz@uni-jena.de
Ilic, Ivan
Oschatz, Martin
2024-03-14T12:20:10+00:00
sword
importub
filename=package.tar
c013c1036d2ce379dea1b7f6da968b94
false
true
CC-BY - Namensnennung 4.0 International
Ivan Ilic
Konstantin Schutjajew
Wuyong Zhang
Martin Oschatz
eng
uncontrolled
Hard carbons
eng
uncontrolled
Sodium-ion batteries
eng
uncontrolled
Anodes
eng
uncontrolled
Microporosity
eng
uncontrolled
Ball milling
Chemie und zugeordnete Wissenschaften
Institut für Chemie
Referiert
Import
Hybrid Open-Access
62963
2022
2022
eng
40
2
9
article
MDPI
Basel
1
2022-02-02
2022-02-02
--
Optical Biomedical Diagnostics Using Lab-on-Fiber Technology
Point-of-care and in-vivo bio-diagnostic tools are the current need for the present critical scenarios in the healthcare industry. The past few decades have seen a surge in research activities related to solving the challenges associated with precise on-site bio-sensing. Cutting-edge fiber optic technology enables the interaction of light with functionalized fiber surfaces at remote locations to develop a novel, miniaturized and cost-effective lab on fiber technology for bio-sensing applications. The recent remarkable developments in the field of nanotechnology provide innumerable functionalization methodologies to develop selective bio-recognition elements for label free biosensors. These exceptional methods may be easily integrated with fiber surfaces to provide highly selective light-matter interaction depending on various transduction mechanisms. In the present review, an overview of optical fiber-based biosensors has been provided with focus on physical principles used, along with the functionalization protocols for the detection of various biological analytes to diagnose the disease. The design and performance of these biosensors in terms of operating range, selectivity, response time and limit of detection have been discussed. In the concluding remarks, the challenges associated with these biosensors and the improvement required to develop handheld devices to enable direct target detection have been highlighted.
Photonics : open access journal
a review
10.3390/photonics9020086
2304-6732
outputup:dataSource:WoS:2022
86
WOS:000764648100001
Gupta, BD (corresponding author), Indian Inst Technol Delhi, Phys Dept, New Delhi 110016, India., bdgupta@physics.iitd.ac.in; pathak@uni-potsdam.de; <br /> anandmoh@post.bgu.ac.il
Gupta, Banshi D.
2024-03-14T12:22:13+00:00
sword
importub
filename=package.tar
3c577bc908f2065221b13c7b1a9764ad
false
true
CC-BY - Namensnennung 4.0 International
Banshi D. Gupta
Anisha Pathak
Anand Shrivastav
eng
uncontrolled
fiber optic sensors
eng
uncontrolled
synthesis
eng
uncontrolled
interferometry
eng
uncontrolled
fluorescence
eng
uncontrolled
SERS
eng
uncontrolled
SPR
eng
uncontrolled
immunosensors
eng
uncontrolled
enzymatic sensors
eng
uncontrolled
molecular imprinted polymers
Institut für Physik und Astronomie
Institut für Chemie
Referiert
Import
Gold Open-Access
DOAJ gelistet
62969
2023
eng
2161
2171
11
13
37
article
Taylor & Francis
London [u.a.]
1
2022-02-09
2022-02-09
--
A new C-C linked benzophenathridine-2-quinoline dimer, and the antiplasmodial activity of alkaloids from Zanthoxylum holstzianum
The CH2Cl2/MeOH (1:1) extract of Zanthoxylum holstzianum stem bark showed good antiplasmodial activity (IC50 2.5 +/- 0.3 and 2.6 +/- 0.3 mu g/mL against the W2 and D6 strains of Plasmodium falciparum, respectively). From the extract five benzophenanthridine alkaloids [8-acetonyldihydrochelerythrine (1), nitidine (2), dihydrochelerythine (3), norchelerythrine (5), arnottianamide (8)]; a 2-quinolone alkaloid [N-methylflindersine (4)]; a lignan [4,4 '-dihydroxy-3,3 '-dimethoxylignan-9,9 '-diyl diacetate (7)] and a dimer of a benzophenanthridine and 2-quinoline [holstzianoquinoline (6)] were isolated. The CH2Cl2/MeOH (1:1) extract of the root bark afforded 1, 3-6, 8, chelerythridimerine (9) and 9-demethyloxychelerythrine (10). Holstzianoquinoline (6) is new, and is the second dimer linked by a C-C bond of a benzophenanthridine and a 2-quinoline reported thus far. The compounds were identified based on spectroscopic evidence. Amongst five compounds (1-5) tested against two strains of P. falciparum, nitidine (IC50 0.11 +/- 0.01 mu g/mL against W2 and D6 strains) and norchelerythrine (IC50 value of 0.15 +/- 0.01 mu g/mL against D6 strain) were the most active.
Natural product research
10.1080/14786419.2022.2034810
35139708
1478-6419
1478-6427
outputup:dataSource:WoS:2022
WOS:000753835000001
Yenesew, Abiy (corresponding author), Univ Nairobi, Dept Chem, Nairobi, Kenya., ayenesew@uonbi.ac.ke
German Academic Exchange Services (DAAD) through the Natural Products; Research Network for Eastern and Central Africa (NAPRECA); International; Science Program (ISP Sweden) [KEN-02]; Kenya Medical Research; Institute's Internal Research Grant [L-183]
Yenesew, Abiy
2024-03-14T13:28:05+00:00
sword
importub
filename=package.tar
467c368e0d7d9906438fa347b31ce2bf
false
true
Denis Akampurira
Hoseah M. Akala
Solomon Derese
Matthias Heydenreich
Abiy Yenesew
eng
uncontrolled
Antiplasmodial
eng
uncontrolled
benzophenanthridine alkaloid
eng
uncontrolled
holstzianoquinoline;
eng
uncontrolled
rutaceae
eng
uncontrolled
Zanthoxylum holstzianum
Chemie und zugeordnete Wissenschaften
Institut für Chemie
Referiert
Import
62919
2021
2021
eng
1548
1556
9
3
54
article
American Chemical Society
Washington
1
2021-01-19
2021-01-19
--
Poly(sulfobetaine) versus poly(N-isopropylmethacrylamide)
The swelling and co-nonsolvency behaviors in pure H2O and in a mixed H2O/CH3OH vapor atmosphere of two different polar, water-soluble polymers in thin film geometry are studied in situ. Films of a zwitterionic poly(sulfobetaine), namely, poly[3-((2-(methacryloyloxy)ethyl)dimethylammonio) propane-1-sulfonate] (PSPE), and a polar nonionic polymer, namely, poly(N-isopropylmethacrylamide) (PNIPMAM), are investigated in real time by spectral reflectance (SR) measurements and Fourier transform infrared (FTIR) spectroscopy. Whereas PSPE is insoluble in methanol, PNIPMAM is soluble but exhibits cononsolvency behavior in water/methanol mixtures. First, the swelling of PSPE and PNIPMAM thin films in H2O vapor is followed. Subsequently, CH3OH is added to the vapor atmosphere, and its contracting effect on the water-swollen films is monitored, revealing a co-nonsolvency-type behavior for PNIPMAM and PSPE. SR measurements indicate that PSPE and PNIPMAM behave significantly different during the H2O swelling and subsequent exposure to CH3OH, not only with respect to the amounts of absorbed water and CH3OH, but also to the cosolvent-induced contraction mechanisms. While PSPE thin films exhibit an abrupt one-step contraction, the contraction of PNIPMAM thin films occurs in two steps. FTIR studies corroborate these findings on a molecular scale and reveal the role of the specific functional groups, both during the swelling and the cosolvent-induced switching of the solvation state.
Macromolecules : a publication of the American Chemical Society
co-nonsolvency-type behavior of thin films in a water/methanol atmosphere
10.1021/acs.macromol.0c02281
0024-9297
1520-5835
outputup:dataSource:WoS:2021
WOS:000618908000041
Müller-Buschbaum, Peter (corresponding author), Tech Univ Munich, Phys Dept, Lehrstuhl Funkt Mat, D-85748 Garching, Germany.; Muller-Buschbaum, P (corresponding author), Tech Univ Munich, Heinz Maier Leibnitz Zentrum MLZ, D-85748 Garching, Germany., muellerb@ph.tum.de
Deutsche Forschungsgemeinschaft (DFG)German Research Foundation (DFG) [LA 611/16-1, MU 1487/29-1, PA 771/20-1]; German Ministry for Education and Research (BMBF) project "FlexiProbe"Federal Ministry of Education & Research (BMBF) [05 K2016]
Müller-Buschbaum, Peter
2024-03-11T07:21:42+00:00
sword
importub
filename=package.tar
7a088493ccce9b65f0f477c3232aeff0
false
true
Lucas Kreuzer
Christoph Lindenmeir
Christina Geiger
Tobias Widmann
Viet Hildebrand
André Laschewsky
Christine M. Papadakis
Peter Müller-Buschbaum
Chemie und zugeordnete Wissenschaften
Institut für Chemie
Referiert
Import
61678
2020
2020
eng
1895
1901
7
4
117
article
National Academy of Sciences
Washington, DC
1
2020-01-13
2020-01-13
--
Polymeric sheet actuators with programmable bioinstructivity
Stem cells are capable of sensing and processing environmental inputs, converting this information to output a specific cell lineage through signaling cascades. Despite the combinatorial nature of mechanical, thermal, and biochemical signals, these stimuli have typically been decoupled and applied independently, requiring continuous regulation by controlling units. We employ a programmable polymer actuator sheet to autonomously synchronize thermal and mechanical signals applied to mesenchymal stem cells (MSC5). Using a grid on its underside, the shape change of polymer sheet, as well as cell morphology, calcium (Ca2+) influx, and focal adhesion assembly, could be visualized and quantified. This paper gives compelling evidence that the temperature sensing and mechanosensing of MSC5 are interconnected via intracellular Ca2+. Up-regulated Ca2+ levels lead to a remarkable alteration of histone H3K9 acetylation and activation of osteogenic related genes. The interplay of physical, thermal, and biochemical signaling was utilized to accelerate the cell differentiation toward osteogenic lineage. The approach of programmable bioinstructivity provides a fundamental principle for functional biomaterials exhibiting multifaceted stimuli on differentiation programs. Technological impact is expected in the tissue engineering of periosteum for treating bone defects.
PNAS
10.1073/pnas.1910668117
1091-6490
31932451
Nan Ma
Andreas Lendlein
Helmholtz Association of German Research Centers (through program-oriented funding); Helmholtz Cross Program Initiative “Technology and Medicine Adaptive Systems”; Helmholtz Virtual Institute; Multifunctional Biomaterials for Medicine (Grant VH-VI-423); Federal Ministry of Education and Research, Germany (Grant 13GW0098, and Project 0315696A “Poly4BioBB”)
209104-5
<a href="https://doi.org/10.25932/publishup-51549">Zweitveröffentlichung in der Schriftenreihe Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe ; 1441</a>
CC-BY - Namensnennung 4.0 International
Zijun Deng
Weiwei Wang
Xun Xua
Oliver E. C. Gould
Karl Kratz
Nan Ma
Andreas Lendlein
eng
uncontrolled
reversible shape-memory actuator
eng
uncontrolled
mesenchymal stem cells
eng
uncontrolled
calcium influx
eng
uncontrolled
HDAC1
eng
uncontrolled
RUNX2
Informatik, Informationswissenschaft, allgemeine Werke
Naturwissenschaften und Mathematik
Biowissenschaften; Biologie
Institut für Chemie
Referiert
Gold Open-Access
62891
2021
2021
eng
790
795
6
33
6
article
Springer Nature Switzerland AG
Cham
1
2021-06-04
2021-06-04
--
Degradation kinetics of oligo(ε-caprolactone) ultrathin films
The potential of using crystallinity as morphological parameter to control polyester degradation in acidic environments is explored in ultrathin films by Langmuir technique. Films of hydroxy or methacrylate end-capped oligo(epsilon-caprolactone) (OCL) are prepared at the air-water interface as a function of mean molecular area (MMA). The obtained amorphous, partially crystalline or highly crystalline ultrathin films of OCL are hydrolytically degraded at pH similar to 1.2 on water surface or on silicon surface as-transferred films. A high crystallinity reduces the hydrolytic degradation rate of the films on both water and solid surfaces. Different acceleration rates of hydrolytic degradation of semi-crystalline films are achieved either by crystals complete melting, partially melting, or by heating them below their melting temperatures. Semi-crystalline OCL films transferred via water onto a solid surface retain their crystalline morphology, degrade in a controlled manner, and are of interest as thermoswitchable coatings for cell substrates and medical devices.
MRS advances : a journal of the Materials Research Society (MRS)
Influence of crystallinity
10.1557/s43580-021-00067-4
2059-8521
outputup:dataSource:WoS:2021
WOS:000658112800001
Lendlein, Andreas (corresponding author), Helmholtz Zentrum Hereon, Inst Act Polymers, D-14513 Teltow, Germany.; Lendlein, Andreas (corresponding author), Helmholtz Zentrum Hereon, Berlin Brandenburg Ctr Regenerat Therapies, D-14513 Teltow, Germany.; Lendlein, A (corresponding author), Univ Potsdam, Inst Chem, D-14476 Potsdam, Germany., lendlein@uni-potsdam.de
Helmholtz Association of German Research Centers through program-oriented funding; Helmholtz Association of German Research Centers through Helmholtz Graduate School for Macromolecular Bioscience (MacroBio) [VH-GS-503]
Lendlein, Andreas
2024-03-07T08:16:20+00:00
sword
importub
filename=package.tar
68cc23626edaaa3405382d839cb94e03
false
true
CC-BY - Namensnennung 4.0 International
Shivam Saretia
Rainhard Gabriel Machatschek
Andreas Lendlein
Chemie und zugeordnete Wissenschaften
Institut für Chemie
Referiert
Import
Hybrid Open-Access
62861
2022
2022
eng
13467
13476
10
31
126
article
American Chemical Society
Washington
1
2022-07-28
2022-07-28
--
Structure and Reactivity of a-Al2O3(0001) Surfaces: How Do Al-I and Gibbsite-like Terminations Interconvert?
The alpha-Al2O3(0001) surface has been extensively studied because of its significance in both fundamental research and application. Prior work suggests that in ultra-high-vacuum (UHV), in the absence of water, the so-called Al-I termination is thermodynamically favored, while in ambient, in contact with liquid water, a Gibbsite-like layer is created. While the view of the alpha- Al2O3(0001)/H2O(l) interface appears relatively clear in theory, experimental characterization of this system has resulted in estimates of surface acidity, i.e., isoelectric points, that differ by 4 pH units and surface structure that in some reports has non-hydrogen-bonded surface aluminol (Al-OH) groups and in others does not. In this study, we employed vibrational sum frequency spectroscopy (VSFS) and density functional theory (DFT) simulation to study the surface phonon modes of the differently terminated alpha-Al2O3(0001) surfaces in both UHV and ambient. We find that, on either water dosing of the Al-I in UHV or heat-induced dehydroxylation of the Gibbsite-like in ambient, the surfaces do not interconvert. This observation offers a new explanation for disagreements in prior work on the alpha-Al2O3(0001)/liquid water interface -different preparation methods may create surfaces that do not interconvert-and shows that the surface phonon spectral response offers a novel probe of interfacial hydrogen bonding structure.
The journal of physical chemistry / publ. weekly by the American Chemical Society. C, Energy, materials, and catalysis
10.1021/acs.jpcc.2c03743
1932-7447
1932-7455
outputup:dataSource:WoS:2022
WOS:000842976100001
Tong, YJ (corresponding author), Fritz Haber Inst Max Planck Soc, D-14195 Berlin, Germany.; Tong, YJ (corresponding author), Univ Duisburg Essen, Fac Phys, D-47057 Duisburg, Germany., yujin.tong@uni-due.de
Max Planck Society
Tong, Yujin
2024-03-04T09:44:57+00:00
sword
importub
filename=package.tar
01e43e7dd0d0b39472c5dbe75834ba6a
false
true
CC-BY - Namensnennung 4.0 International
Yanhua Yue
Giacomo Melani
Harald Kirsch
Alexander Paarmann
Peter Saalfrank
Richard Kramer Campen
Yujin Tong
Chemie und zugeordnete Wissenschaften
Institut für Chemie
Referiert
Import
Hybrid Open-Access