Institution
Nanosystems Initiative Munich
Facility•Munich, Germany•
About: Nanosystems Initiative Munich is a facility organization based out in Munich, Germany. It is known for research contribution in the topics: Quantum dot & Perovskite (structure). The organization has 323 authors who have published 549 publications receiving 24316 citations.
Topics: Quantum dot, Perovskite (structure), Exciton, Nanowire, Charge carrier
Papers
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TL;DR: It is proposed that employing a hydroxyl anion/radical redox couple to efficiently relay the hole from the semiconductor to the scavenger leads to a marked increase in the H2 generation rate without using expensive noble metal co-catalysts.
Abstract: Photocatalytic efficiency can be limited by slow transfer of photoexcited holes and high charge recombination rates. Using a hydroxyl anion–radical redox couple leads to enhanced photocatalytic H2 generation on Ni-decorated CdS nanorods. Photocatalytic conversion of solar energy to fuels, such as hydrogen, is attracting enormous interest, driven by the promise of addressing both energy supply and storage1. Colloidal semiconductor nanocrystals have been at the forefront of these efforts owing to their favourable and tunable optical and electronic properties2,3,4 as well as advances in their synthesis5,6. The efficiency of the photocatalysts is often limited by the slow transfer and subsequent reactions of the photoexcited holes and the ensuing high charge recombination rates. Here we propose that employing a hydroxyl anion/radical redox couple to efficiently relay the hole from the semiconductor to the scavenger leads to a marked increase in the H2 generation rate without using expensive noble metal co-catalysts. The apparent quantum yield and the formation rate under 447 nm laser illumination exceeded 53% and 63 mmol g−1 h−1, respectively. The fast hole transfer confers long-term photostability on the system and opens new pathways to improve the oxidation side of full water splitting.
679 citations
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TL;DR: This work shows that the highly stable, non-toxic and earth-abundant material, ZrSiS, has an electronic band structure that hosts several Dirac cones that form a Fermi surface with a diamond-shaped line of Dirac nodes, making it a very promising candidate to study Dirac electrons, as well as the properties of lines ofDirac nodes.
Abstract: Materials harbouring exotic quasiparticles, such as massless Dirac and Weyl fermions, have garnered much attention from physics and material science communities due to their exceptional physical properties such as ultra-high mobility and extremely large magnetoresistances. Here, we show that the highly stable, non-toxic and earth-abundant material, ZrSiS, has an electronic band structure that hosts several Dirac cones that form a Fermi surface with a diamond-shaped line of Dirac nodes. We also show that the square Si lattice in ZrSiS is an excellent template for realizing new types of two-dimensional Dirac cones recently predicted by Young and Kane. Finally, we find that the energy range of the linearly dispersed bands is as high as 2 eV above and below the Fermi level; much larger than of other known Dirac materials. This makes ZrSiS a very promising candidate to study Dirac electrons, as well as the properties of lines of Dirac nodes.
661 citations
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TL;DR: PTI nanosheets show significantly enhanced visible-light driven photocatalytic activity toward hydrogen evolution compared to their bulk counterpart, which highlights the crucial role of morphology and surface area on the photocatallytic performance of carbon nitride materials.
Abstract: Nanosheets of a crystalline 2D carbon nitride were obtained by ionothermal synthesis of the layered bulk material poly(triazine imide), PTI, followed by one-step liquid exfoliation in water. Triazine-based nanosheets are 1-2 nm in height and afford chemically and colloidally stable suspensions under both basic and acidic conditions. We use solid-state NMR spectroscopy of isotopically enriched, restacked nanosheets as a tool to indirectly monitor the exfoliation process and carve out the chemical changes occurring upon exfoliation, as well as to determine the nanosheet thickness. PTI nanosheets show significantly enhanced visible-light driven photocatalytic activity toward hydrogen evolution compared to their bulk counterpart, which highlights the crucial role of morphology and surface area on the photocatalytic performance of carbon nitride materials.
558 citations
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TL;DR: The simple, scalable, single-step, and polar-solvent-free synthesis of high-quality colloidal CsPbX3 (X=Cl, Br, and I) perovskite nanocrystals with tunable halide ion composition and thickness by direct ultrasonication of the corresponding precursor solutions in the presence of organic capping molecules is described.
Abstract: We describe the simple, scalable, single-step, and polar-solvent-free synthesis of high-quality colloidal CsPbX3 (X=Cl, Br, and I) perovskite nanocrystals (NCs) with tunable halide ion composition and thickness by direct ultrasonication of the corresponding precursor solutions in the presence of organic capping molecules. High angle annular dark field scanning transmission electron microscopy (HAADF-STEM) revealed the cubic crystal structure and surface termination of the NCs with atomic resolution. The NCs exhibit high photoluminescence quantum yields, narrow emission line widths, and considerable air stability. Furthermore, we investigated the quantum size effects in CsPbBr3 and CsPbI3 nanoplatelets by tuning their thickness down to only three to six monolayers. The high quality of the prepared NCs (CsPbBr3) was confirmed by amplified spontaneous emission with low thresholds. The versatility of this synthesis approach was demonstrated by synthesizing different perovskite NCs.
551 citations
Authors
Showing all 323 results
Name | H-index | Papers | Citations |
---|---|---|---|
Thomas Bein | 109 | 677 | 42800 |
Ernst Wagner | 96 | 537 | 36723 |
Jochen Feldmann | 91 | 417 | 31049 |
Peter Hänggi | 90 | 788 | 42272 |
Markus Fischer | 85 | 490 | 28454 |
Martin Stutzmann | 84 | 781 | 30938 |
Gerhard Abstreiter | 77 | 791 | 25631 |
Oliver Eickelberg | 75 | 329 | 19447 |
Rudolf Gross | 68 | 532 | 17739 |
Dirk Trauner | 65 | 821 | 16279 |
Peter Müller-Buschbaum | 63 | 605 | 17603 |
Bettina V. Lotsch | 62 | 248 | 14599 |
Christoph Bräuchle | 58 | 267 | 12032 |
Jonathan J. Finley | 56 | 353 | 11100 |
Paolo Lugli | 55 | 739 | 14706 |