Search

Data‐intensive discovery of water‐splitting catalysts can accelerate the development of sustainable energy technologies, such as the photocatalytic and/or electrocatalytic production of renewable hydrogen fuel. Through computational screening, 13 materials were recently predicted as potential water‐splitting photocatalysts: Cu3NbS4, CuYS2, SrCu2O2, CuGaO2, Na3BiO4, Sr2PbO4, LaCuOS, LaCuOSe, Na2TeO4, La4O4Se3, Cu2WS4, BaCu2O2, and CuAlO2. Herein, these materials are synthesized, their bandgaps and band alignments are experimentally determined, and their photoelectrocatalytic hydrogen evolution properties are assessed. Using cyclic voltammetry and chopped illumination experiments, 9 of the 13 materials are experimentally found to have bandgaps and band alignments that straddle the potentials required for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), as computationally predicted. During photocatalytic testing, 12 of the materials yield a measurable photocurrent. However, only three are found to be active for the HER, with Cu3NbS4, CuYS2, and Cu2WS4 producing H2 in amounts comparable to bare TiO2; a benchmark photocatalyst. This study provides experimental validation of computational bandgap and band alignment predictions while also successfully identifying active photocatalysts. [ABSTRACT FROM AUTHOR]

Topological materials have high carrier mobilities that can be maintained in the presence of crystal structure defects, which is useful for catalysis. Topological materials have been shown to be active catalysts, but it remains unclear if topology persists during catalysis. We studied the physical and chemical evolution of MoTe2 during photo‐ and electrocatalytic hydrogen production. This material offers a unique opportunity to directly compare a trivial semiconductor, 2H‐MoTe2, with a topological insulator, 1T'‐MoTe2, with comparable compositions, crystal structures, and surface roughnesses. We observed no major bulk changes in the materials after catalysis. The surfaces of the catalysts were significantly roughened and oxidized, but the carrier mobility of the topological phase remained high. These results suggest that topology persists during, and may be advantageous for, catalysis, and provide rationale for considering topology in the search for water‐splitting catalysts. [ABSTRACT FROM AUTHOR]

Alloying metals can achieve enhanced kinetics for the hydrogen evolution reaction (HER), but most known HER alloy catalysts combine metals that are miscible in the bulk. Theoretical studies suggest that bulk‐immiscible AgRh alloys will exhibit near‐zero hydrogen binding energies, which is important for high‐performing HER catalysts. Current routes to AgRh nanoparticles yield only small quantities or require specialized setups. Here, we establish a ligand‐free, scalable synthesis of AgRh nanoparticles and demonstrate their catalytic viability for the HER under acidic conditions. AgRh nanoparticle electrodes exhibited low operating potentials with current densities of −10 and −100 mA/cm2 at overpotentials of −17 and −32 mV, respectively. The electrodes were highly durable with very little change in overpotentials required to maintain hydrogen production for 24 h and after 400 successive cycles. These results establish bulk‐immiscible AgRh alloys as promising non‐Pt HER catalysts. [ABSTRACT FROM AUTHOR]

Nanoscale transition metal tellurides are important materials for a variety of applications. However, solution‐phase methods to synthesize nanoscale transition metal tellurides are not as well‐developed as for related sulfide and selenide systems. Here, we show that pre‐formed colloidal metal nanoparticles react with bis(trimethylsilyl)telluride to form their corresponding tellurides. Nanoparticles of Pd, Pt, and Ni convert to nanoscale particles of the layered transition metal dichalcogenides PdTe2, PtTe2, and NiTe2 upon reaction with bis(trimethylsilyl)telluride. When Pd nanoparticles instead react with a TOP‐Te complex (TOP = trioctylphosphine), PdTe forms. This result demonstrates that the metal telluride phase that forms can be controlled by the reactivity of the tellurium reagent. Other nanoparticles, including Co, Ag, and Rh, also form crystalline metal tellurides upon reaction with bis(trimethylsilyl)telluride, which indicates that this approach to synthesizing nanoscale transition metal tellurides is general. [ABSTRACT FROM AUTHOR]

The M1 form of vanadium dioxide, which exhibits a reversible insulator-metal transition above room temperature, has been incorporated into nanoscale heterostructures through solution-phase epitaxial growth on the tips of rutile TiO2 nanorods. Four distinct classes of VO2-TiO2-VO2 nanorod heterostructures are accessible by modulating the growth conditions. Each type of VO2-TiO2-VO2 nanostructure has a different insulator-metal transition temperature that depends on the VO2 domain sizes and the TiO2-VO2 interfacial strain characteristics. [ABSTRACT FROM AUTHOR]

A fundamental understanding of the behavior of non-noble based materials toward the hydrogen evolution reaction is crucial for the successful implementation into practical devices. Through the implementation of a highly sensitive inductively coupled plasma mass spectrometer coupled to a scanning flow cell, the activity and stability of non-noble electrocatalysts is presented. The studied catalysts comprise a range of compositions, including metal carbides (WC), sulfides (MoS2), phosphides (Ni5P4, Co2P), and their base metals (W, Ni, Mo, Co); their activity, stability, and degradation behavior was elaborated and compared to the state-of-the-art catalyst platinum. The non-noble materials are stable at HER potentials but dissolve substantially when no current is flowing. Through pre- and post-characterization of the catalysts, explanations of their stability (thermodynamics and kinetics) are discussed, challenges for the application in real devices are analyzed, and strategies for circumventing dissolution are suggested. The precise correlation of metal dissolution with applied potential/current density allows for narrowing down suitable material choices as replacement for precious group metals as for example, platinum and opens up new ways in finding cost-efficient, active, and stable new-generation electrocatalysts. [ABSTRACT FROM AUTHOR]

The ability to selectively form one crystal structure among several options in a polymorphic system is an important goal in solid-state synthesis. Nanocrystal cation exchange, which proceeds rapidly under mild conditions, can retain key structural features and yield otherwise inaccessible phases, but the extent to which crystal structure can be retained and therefore selectively targeted during such reactions has been limited. Here, we show that nanocrystals of digenite Cu2−xS transform to zincblende MnS and CoS upon cation exchange. Zincblende MnS and CoS, which are metastable in bulk, retain both the tetrahedral cation coordination and cubic close packed anion sublattice of digenite Cu2−xS. Comparison with wurtzite MnS and CoS, which have been accessed previously through analogous cation exchange of roxbyite Cu2−xS, demonstrates the selective formation of the related zincblende vs. wurtzite polymorphs by cation exchange of structurally distinct templates. [ABSTRACT FROM AUTHOR]

Molybdenum ditelluride, MoTe2, is emerging as an important transition-metal dichalcogenide (TMD) material because of its favorable properties relative to other TMDs. The 1T ′ polymorph of MoTe2 is particularly interesting because it is semimetallic with bands that overlap near the Fermi level, but semiconducting 2H-MoTe2 is more stable and therefore more accessible synthetically. Metastable 1T ′-MoTe2 forms directly in solution at 300 °C as uniform colloidal nanostructures that consist of few-layer nanosheets, which appear to exhibit an approx. 1 % lateral lattice compression relative to the bulk analogue. Density functional theory calculations suggest that small grain sizes and polycrystallinity stabilize the 1T ′ phase in the MoTe2 nanostructures and suppress its transformation back to the more stable 2H polymorph through grain boundary pinning. Raman spectra of the 1T ′-MoTe2 nanostructures exhibit a laser energy dependence, which could be caused by electronic transitions. [ABSTRACT FROM AUTHOR]

Ion exchange reactions of colloidal nanocrystals provide access to complex products that are synthetically challenging using traditional hot-injection methods. However, such reactions typically achieve only partial material transformations by employing either cation or anion exchange processes. It is now shown that anion and cation exchange reactions can be coupled together and applied sequentially in one integrated pathway that leads to complete material transformations of nanocrystal templates. Although the product nanocrystals do not contain any of the original constituent elements, the original morphology is retained, thereby fully decoupling morphology and composition control. The sequential anion/cation exchange process was applied to pseudo-spherical CdO nanocrystals and ZnO tetrapods, producing fully transformed and shape-controlled nanocrystals of copper and silver sulfides and selenides. Furthermore, hollow core-shell tetrapod ZnS@CdS heterostructures were readily accessible. [ABSTRACT FROM AUTHOR]

Nanoparticles of cobalt phosphide, CoP, have been prepared and evaluated as electrocatalysts for the hydrogen evolution reaction (HER) under strongly acidic conditions (0.50 M H2SO4, pH 0.3). Uniform, multi-faceted CoP nanoparticles were synthesized by reacting Co nanoparticles with trioctylphosphine. Electrodes comprised of CoP nanoparticles on a Ti support (2 mg cm−2 mass loading) produced a cathodic current density of 20 mA cm−2 at an overpotential of −85 mV. The CoP/Ti electrodes were stable over 24 h of sustained hydrogen production in 0.50 M H2SO4. The activity was essentially unchanged after 400 cyclic voltammetric sweeps, suggesting long-term viability under operating conditions. CoP is therefore amongst the most active, acid-stable, earth-abundant HER electrocatalysts reported to date. [ABSTRACT FROM AUTHOR]

Die rege Nachfrage nach komplexen Nanomaterialien mit präzise kontrollierten Architekturen und Grenzflächen hat zu einer enormen Entwicklung bei innovativen Syntheseverfahren geführt. Dieser Aufsatz beleuchtet Schlüsselstrategien für die chemische Umwandlung und schrittweise Synthese von anorganischen Mehrkomponenten ‐ Nanostrukturen, wobei existierende Umwandlungsreaktionen im Nanobereich in Klassen eingeordnet werden, die den bei der Synthese von organischen Molekülen verwendeten entsprechen. Ein Schwerpunkt liegt auf der Übertragung von Konzepten aus der Molekülsynthese auf nanoskalige Systeme: Dazu gehören unter anderem Ortsselektivität, Regio ‐ und Chemoselektivität, orthogonale Reaktivität, Kupplungsreaktionen, Strategien zum Schützen und Entschützen sowie Verfahren zur Trennung und Aufreinigung. Das so geschaffene Regelwerk stellt ein neues Modell für die “Totalsynthese” von komplexen anorganischen Nanostrukturen dar, dem die Prinzipien von mehrstufigen Totalsynthesen komplexer organischer Molekülverbindungen und Naturstoffe zugrundeliegen. Nanoskalige Totalsynthese: Ganz analog zur Totalsynthese von großen und komplexen molekularen Zielverbindungen lassen sich vielfältige Nanopartikel ‐ Reaktionsbibliotheken in „Totalsynthesen“ zum gezielten Aufbau komplexer nanoskaliger Mehrkomponenten ‐ Architekturen nutzen. [ABSTRACT FROM AUTHOR]

New synthetic innovations are rapidly being developed to address the demand for complex, next-generation nanomaterials with rigorously controlled architectures and interfaces. This Review highlights key strategies for the chemical transformation and stepwise synthesis of multicomponent inorganic nanostructures, with the existing nanoscale transformations categorized into classes of reactions that are related to those used in the synthesis of organic molecules. The application of concepts used in molecular synthesis-including site-selectivity, regio- and chemoselectivity, orthogonal reactivity, coupling reactions, protection/deprotection strategies, and procedures for separation and purification-to nanoscale systems is emphasized. Collectively, the resulting synthetic concept represents an emerging model for the synthesis of complex inorganic nanostructures on the basis of the guiding principles that underpin the multistep total synthesis of complex organic molecules and natural products. [ABSTRACT FROM AUTHOR]

The cover page of the journal "Angewandte Chemie" is presented.

Review: 197 refs. [ABSTRACT FROM AUTHOR]

Review: 91 refs. [ABSTRACT FROM AUTHOR]

Topological materials have high carrier mobilities that can be maintained in the presence of crystal structure defects, which is useful for catalysis. Topological materials have been shown to be active catalysts, but it remains unclear if topology persists during catalysis. We studied the physical and chemical evolution of MoTe2 during photo‐ and electrocatalytic hydrogen production. This material offers a unique opportunity to directly compare a trivial semiconductor, 2H‐MoTe2, with a topological insulator, 1T'‐MoTe2, with comparable compositions, crystal structures, and surface roughnesses. We observed no major bulk changes in the materials after catalysis. The surfaces of the catalysts were significantly roughened and oxidized, but the carrier mobility of the topological phase remained high. These results suggest that topology persists during, and may be advantageous for, catalysis, and provide rationale for considering topology in the search for water‐splitting catalysts. [ABSTRACT FROM AUTHOR]