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Anna Fischer

Bio: Anna Fischer is an academic researcher from University of Freiburg. The author has contributed to research in topics: Catalysis & Mesoporous material. The author has an hindex of 32, co-authored 101 publications receiving 6968 citations. Previous affiliations of Anna Fischer include Max Planck Society & Centre national de la recherche scientifique.


Papers
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TL;DR: In this paper, high resolution transmission electron microscopy proves the extended two-dimensional character of the condensation motif of graphitic carbon nitride, and a new family of metal nitride nanostructures can also be accessed from the corresponding oxides.
Abstract: Graphitic carbon nitride, g-C3N4, can be made by polymerization of cyanamide, dicyandiamide or melamine. Depending on reaction conditions, different materials with different degrees of condensation, properties and reactivities are obtained. The firstly formed polymeric C3N4 structure, melon, with pendant amino groups, is a highly ordered polymer. Further reaction leads to more condensed and less defective C3N4 species, based on tri-s-triazine (C6N7) units as elementary building blocks. High resolution transmission electron microscopy proves the extended two-dimensional character of the condensation motif. Due to the polymerization-type synthesis from a liquid precursor, a variety of material nanostructures such as nanoparticles or mesoporous powders can be accessed. Those nanostructures also allow fine tuning of properties, the ability for intercalation, as well as the possibility to give surface-rich materials for heterogeneous reactions. Due to the special semiconductor properties of carbon nitrides, they show unexpected catalytic activity for a variety of reactions, such as for the activation of benzene, trimerization reactions, and also the activation of carbon dioxide. Model calculations are presented to explain this unusual case of heterogeneous, metal-free catalysis. Carbon nitride can also act as a heterogeneous reactant, and a new family of metal nitride nanostructures can be accessed from the corresponding oxides.

2,746 citations

Journal ArticleDOI
TL;DR: In this paper, an electrodeposited Mn oxide (MnCat) was reported to catalyzes electrochemical water oxidation at neutral pH at rates that approach the level needed for direct coupling to photoactive materials.
Abstract: In the sustainable production of non-fossil fuels, water oxidation is pivotal. Development of efficient catalysts based on manganese is desirable because this element is earth-abundant, inexpensive, and largely non-toxic. We report an electrodeposited Mn oxide (MnCat) that catalyzes electrochemical water oxidation at neutral pH at rates that approach the level needed for direct coupling to photoactive materials. By choice of the voltage protocol we could switch between electrodeposition of inactive Mn oxides (deposition at constant anodic potentials) and synthesis of the active MnCat (deposition by voltage-cycling protocols). Electron microscopy reveals that the MnCat consists of nanoparticles (100 nm) with complex fine-structure. X-ray spectroscopy reveals that the amorphous MnCat resembles the biological paragon, the water-splitting Mn4Ca complex of photosynthesis, with respect to mean Mn oxidation state (ca. +3.8 in the MnCat) and central structural motifs. Yet the MnCat functions without calcium or other bivalent ions. Comparing the MnCat with electrodeposited Mn oxides inactive in water oxidation, we identify characteristics that likely are crucial for catalytic activity. In both inactive Mn oxides and active ones (MnCat), extensive di-μ-oxo bridging between Mn ions is observed. However in the MnCat, the voltage-cycling protocol resulted in formation of MnIII sites and prevented formation of well-ordered and unreactive MnIVO2. Structure–function relations in Mn-based water-oxidation catalysts and strategies to design catalytically active Mn-based materials are discussed. Knowledge-guided performance optimization of the MnCat could pave the road for its technological use.

406 citations

Journal ArticleDOI
TL;DR: In this article, photoactive condensed carbon nitride nanorods (CNRs) can be obtained via confined thermal condensation of cyanamide inside the nanochannels of an anodic alumni oxide (AAO) membrane template.
Abstract: Photoactive, condensed carbon nitride nanorods (CNRs) can be obtained via confined thermal condensation of cyanamide inside the nanochannels of an anodic alumni oxide (AAO) membrane template. The promotion of a more condensed network of CNRs with lowered HOMO in water splitting (including both H2 and O2 revolution) and photocurrent output was demonstrated.

373 citations


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TL;DR: It is shown that an abundant material, polymeric carbon nitride, can produce hydrogen from water under visible-light irradiation in the presence of a sacrificial donor.
Abstract: The production of hydrogen from water using a catalyst and solar energy is an ideal future energy source, independent of fossil reserves. For an economical use of water and solar energy, catalysts that are sufficiently efficient, stable, inexpensive and capable of harvesting light are required. Here, we show that an abundant material, polymeric carbon nitride, can produce hydrogen from water under visible-light irradiation in the presence of a sacrificial donor. Contrary to other conducting polymer semiconductors, carbon nitride is chemically and thermally stable and does not rely on complicated device manufacturing. The results represent an important first step towards photosynthesis in general where artificial conjugated polymer semiconductors can be used as energy transducers.

9,751 citations

Journal ArticleDOI
TL;DR: It is anticipated that this review can stimulate a new research doorway to facilitate the next generation of g-C3N4-based photocatalysts with ameliorated performances by harnessing the outstanding structural, electronic, and optical properties for the development of a sustainable future without environmental detriment.
Abstract: As a fascinating conjugated polymer, graphitic carbon nitride (g-C3N4) has become a new research hotspot and drawn broad interdisciplinary attention as a metal-free and visible-light-responsive photocatalyst in the arena of solar energy conversion and environmental remediation. This is due to its appealing electronic band structure, high physicochemical stability, and “earth-abundant” nature. This critical review summarizes a panorama of the latest progress related to the design and construction of pristine g-C3N4 and g-C3N4-based nanocomposites, including (1) nanoarchitecture design of bare g-C3N4, such as hard and soft templating approaches, supramolecular preorganization assembly, exfoliation, and template-free synthesis routes, (2) functionalization of g-C3N4 at an atomic level (elemental doping) and molecular level (copolymerization), and (3) modification of g-C3N4 with well-matched energy levels of another semiconductor or a metal as a cocatalyst to form heterojunction nanostructures. The constructi...

5,054 citations

Journal ArticleDOI
TL;DR: The unique advances on ultrathin 2D nanomaterials are introduced, followed by the description of their composition and crystal structures, and the assortments of their synthetic methods are summarized.
Abstract: Since the discovery of mechanically exfoliated graphene in 2004, research on ultrathin two-dimensional (2D) nanomaterials has grown exponentially in the fields of condensed matter physics, material science, chemistry, and nanotechnology. Highlighting their compelling physical, chemical, electronic, and optical properties, as well as their various potential applications, in this Review, we summarize the state-of-art progress on the ultrathin 2D nanomaterials with a particular emphasis on their recent advances. First, we introduce the unique advances on ultrathin 2D nanomaterials, followed by the description of their composition and crystal structures. The assortments of their synthetic methods are then summarized, including insights on their advantages and limitations, alongside some recommendations on suitable characterization techniques. We also discuss in detail the utilization of these ultrathin 2D nanomaterials for wide ranges of potential applications among the electronics/optoelectronics, electrocat...

3,628 citations

Journal ArticleDOI
27 Feb 2015-Science
TL;DR: The design and fabrication of a metal-free carbon nanodot–carbon nitride (C3N4) nanocomposite is reported and its impressive performance for photocatalytic solar water splitting is demonstrated.
Abstract: The use of solar energy to produce molecular hydrogen and oxygen (H2 and O2) from overall water splitting is a promising means of renewable energy storage. In the past 40 years, various inorganic and organic systems have been developed as photocatalysts for water splitting driven by visible light. These photocatalysts, however, still suffer from low quantum efficiency and/or poor stability. We report the design and fabrication of a metal-free carbon nanodot-carbon nitride (C3N4) nanocomposite and demonstrate its impressive performance for photocatalytic solar water splitting. We measured quantum efficiencies of 16% for wavelength λ = 420 ± 20 nanometers, 6.29% for λ = 580 ± 15 nanometers, and 4.42% for λ = 600 ± 10 nanometers, and determined an overall solar energy conversion efficiency of 2.0%. The catalyst comprises low-cost, Earth-abundant, environmentally friendly materials and shows excellent stability.

3,553 citations

Journal ArticleDOI
TL;DR: In this article, a top-down thermal oxidation etching of bulk g-C3N4 in air has been shown to improve the photocatalytic activities of the material in terms of OH radical generation and hydrogen evolution.
Abstract: Graphitic (g)-C3N4 with a layered structure has the potential of forming graphene-like nanosheets with unusual physicochemical properties due to weak van der Waals forces between layers. Herein is shown that g-C3N4 nanosheets with a thickness of around 2 nm can be easily obtained by a simple top-down strategy, namely, thermal oxidation etching of bulk g-C3N4 in air. Compared to the bulk g-C3N4, the highly anisotropic 2D-nanosheets possess a high specific surface area of 306 m2 g-1, a larger bandgap (by 0.2 eV), improved electron transport ability along the in-plane direction, and increased lifetime of photoexcited charge carriers because of the quantum confinement effect. As a consequence, the photocatalytic activities of g-C3N4 nanosheets have been remarkably improved in terms of OH radical generation and photocatalytic hydrogen evolution.

2,900 citations