Angelika Brückner
University of Rostock
267 Papers
1.6K Citations
Angelika Brückner is an academic researcher from University of Rostock. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 53, co-authored 250 publications. Previous affiliations of Angelika Brückner include Catalan Institution for Research and Advanced Studies & Leibniz Association.
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Papers
Simultaneously Tuning the Defects and Surface Properties of Ta 3 N 5 Nanoparticles by Mg-Zr Codoping for Significantly Accelerated Photocatalytic H 2 Evolution.
Jiadong Xiao,Junie Jhon M. Vequizo,Takashi Hisatomi,Jabor Rabeah,Mamiko Nakabayashi,Zheng Wang,Zheng Wang,Qi Xiao,Huihui Li,Huihui Li,Zhenhua Pan,Mary Krause,Nick Yin,Gordon S. Smith,Naoya Shibata,Angelika Brückner,Akira Yamakata,Tsuyoshi Takata,Kazunari Domen,Kazunari Domen +19 more
TL;DR: In this article, the authors synthesized Mg-Zr-codoped single-crystalline Ta3N5 nanoparticles by a brief NH3 nitridation process, exhibiting photocatalytic water reduction activity 45 times greater than that of pristine Ta 3N5 under visible light.
Relations between Structure, Activity and Stability in C3N4 Based Photocatalysts Used for Solar Hydrogen Production
Ramesh P. Sivasankaran,Nils Rockstroh,Dirk Hollmann,Carsten Kreyenschulte,Giovanni Agostini,Henrik Lund,Amitava Acharjya,Jabor Rabeah,Ursula Bentrup,Henrik Junge,Arne Thomas,Angelika Brückner +11 more
Abstract: Solar hydrogen production from water could be a sustainable and environmentally friendly alternative to fossil energy carriers, yet so far photocatalysts active and stable enough for large-scale applications are not available, calling for advanced research efforts. In this work, H2 evolution rates of up to 1968 and 5188 μmol h−1 g−1 were obtained from aqueous solutions of triethanolamine (TEOA) and oxalic acid (OA), respectively, by irradiating composites of AgIn5S8 (AIS), mesoporous C3N4 (CN, surface area >150 m2/g) and ≤2 wt.% in-situ photodeposited Pt nanoparticles (NPs) with UV-vis (≥300 nm) and pure visible light (≥420 nm). Structural properties and electron transport in these materials were analyzed by XRD, STEM-HAADF, XPS, UV-vis-DRS, ATR-IR, photoluminescence and in situ-EPR spectroscopy. Initial H2 formation rates were highest for Pt/CN, yet with TEOA this catalyst deactivated by inclusion of Pt NPs in the matrix of CN (most pronounced at λ ≥ 300 nm) while it remained active with OA, since in this case Pt NPs were enriched on the outermost surface of CN. In Pt/AIS-CN catalysts, Pt NPs were preferentially deposited on the surface of the AIS phase which prevents them from inclusion in the CN phase but reduces simultaneously the initial H2 evolution rate. This suggests that AIS hinders transport of separated electrons from the CN conduction band to Pt NPs but retains the latter accessible by protons to produce H2.
Deactivation of a commercial catalyst in the epoxidation of ethylene to ethylene oxide—basis for accelerated testing
TL;DR: An accelerated deactivation procedure for a commercial Ag-based catalyst for ethylene epoxidation was developed in a gradientless Berty-recycle reactor by increasing temperature and oxygen concentration which, however, were kept constant in the whole reactor for a single experiment.
Photoassisted Ti ? O Activation in a Decamethyltitanocene Dihydroxido Complex: Insights into the Elemental Steps of Water Splitting
Monty Kessler,Stefanie Schüler,Dirk Hollmann,Marcus Klahn,Torsten Beweries,Anke Spannenberg,Angelika Brückner,Uwe Rosenthal +7 more
TL;DR: The conversion of sunlight into chemical energy is a very promising research topic, and the discovery of the Honda–Fujishima effect describes the photoassisted generation of dihydrogen and dioxygen from water using a TiO2/Pt electrode array.
Highly dispersed VOx species on mesoporous supports: Promising catalysts for the oxidative dehydrogenation (ODH) of propane
TL;DR: In this article, a mesoporous Al2O3, SBA-15 and MCM-48 materials have been studied by simultaneous in situ-EPR/UV-vis/on line GC measurements and tested as catalysts for the ODH of propane.