Polyethylene hydrogenolysis by dilute RuPt alloy to achieve H-pressure-independent low methane selectivity.

Chemical recycling of plastic waste could reduce its environmental impact and create a more sustainable society. Hydrogenolysis is a viable method for polyolefin valorization but typically requires high hydrogen pressures to minimize methane production. Here, we circumvent this stringent requirement using dilute RuPt alloy to suppress the undesired terminal C-C scission under hydrogen-lean conditions.

Expedient alkyne semi-hydrogenation by using a bimetallic AgCu-CN single atom catalyst.

Metal-catalyzed semi-hydrogenation of alkynes is an important step in organic synthesis to produce diverse chemical compounds. However, conventional noble metal catalysts often suffer from poor selectivity owing to over-hydrogenation. Here, we demonstrate a high-loading bimetallic AgCu-CN single-atom catalyst (SAC) for alkyne semi-hydrogenation.

Opportunities and challenges for plastic depolymerization by biomimetic catalysis.

Plastic waste has imposed significant burdens on the environment. Chemical recycling allows for repeated regeneration of plastics without deterioration in quality, but often requires harsh reaction conditions, thus being environmentally unfriendly. Enzymatic catalysis offers a promising solution for recycling under mild conditions, but it faces inherent limitations such as poor stability, high cost, and narrow substrate applicability.

Ammonia Electrosynthesis from Nitrate Using a Ruthenium-Copper Cocatalyst System: A Full Concentration Range Study.

Electrochemical synthesis of ammonia via the nitrate reduction reaction (NO3RR) has been intensively researched as an alternative to the traditional Haber-Bosch process. Most research focuses on the low concentration range representative of the nitrate level in wastewater, leaving the high concentration range, which exists in nuclear and fertilizer wastes, unexplored. The use of a concentrated electrolyte (≥1 M) for higher rate production is hampered by poor hydrogen transfer kinetics.

Diatomic iron nanozyme with lipoxidase-like activity for efficient inactivation of enveloped virus.

Enveloped viruses encased within a lipid bilayer membrane are highly contagious and can cause many infectious diseases like influenza and COVID-19, thus calling for effective prevention and inactivation strategies. Here, we develop a diatomic iron nanozyme with lipoxidase-like (LOX-like) activity for the inactivation of enveloped virus. The diatomic iron sites can destruct the viral envelope via lipid peroxidation, thus displaying non-specific virucidal property.

Addressing the quantitative conversion bottleneck in single-atom catalysis.

Single-atom catalysts (SACs) offer many advantages, such as atom economy and high chemoselectivity; however, their practical application in liquid-phase heterogeneous catalysis is hampered by the productivity bottleneck as well as catalyst leaching. Flow chemistry is a well-established method to increase the conversion rate of catalytic processes, however, SAC-catalysed flow chemistry in packed-bed type flow reactor is disadvantaged by low turnover number and poor stability. In this study, we demonstrate the use of fuel cell-type flow stacks enabled exceptionally high quantitative conversion in single atom-catalyzed reactions, as exemplified by the use of Pt SAC-on-MoS/graphite felt catalysts incorporated in flow cell.

Conductive, Large-Area, and Continuous 7,7,8,8-Tetracyanoquinodimethane@HKUST-1 Thin Films Fabricated Using Solution Shearing.

Most metal-organic frameworks (MOFs) have an insulating nature due to their porosity and redox-inactive organic components. The electrical conductivity of the prototypical MOF, HKUST-1, can be tuned by infiltrating a small-molecule organic semiconductor, 7,7,8,8-tetracyanoquinodimethane (TCNQ), into the HKUST-1 pores, creating TCNQ@HKUST-1. However, current processes of creating TCNQ@HKUST-1 films have many roadblocks such as slow crystallization rates, which limit high throughput production, and the formation of Cu(TCNQ) as a byproduct, which affects the electrical conductivity and degrades the chemical structure of HKUST-1.

Fabrication of copper phthalocyanine/reduced graphene oxide nanocomposites for efficient photocatalytic reduction of hexavalent chromium.

Copper(II) phthalocyanine (CuPc) and non-peripheral octamethyl-substituted copper(II) phthalocyanine (N-CuMePc) were combined with reduced graphene oxide (rGO) via a precipitation method to form CuPc/rGO and N-CuMePc/rGO nanocomposites, respectively. CuPc nanorods are distributed on rGO, and N-CuMePc exists as nanorods and nanoparticles on rGO. The Cr(VI) removal ratio of N-CuMePc/rGO exposed in simulated sunlight is 99.

Dual Defect-Passivation Using Phthalocyanine for Enhanced Efficiency and Stability of Perovskite Solar Cells.

Semiconducting molecules have been employed to passivate traps extant in the perovskite film for enhancement of perovskite solar cells (PSCs) efficiency and stability. A molecular design strategy to passivate the defects both on the surface and interior of the CH NH PbI perovskite layer, using two phthalocyanine (Pc) molecules (NP-SC -ZnPc and NP-SC -TiOPc) is demonstrated. The presence of lone electron pairs on S, N, and O atoms of the Pc molecular structures provides the opportunity for Lewis acid-base interactions with under-coordinated Pb sites, leading to efficient defect passivation of the perovskite layer.

In situ synthesis of N-CoMePc/rGO nanocomposite with enhanced photocatalytic activity and stability in Cr(VI) reduction.

Graphene-based composites are widely used in the photocatalytic treatment of heavy-metal ions or dyes. In this study, we developed a facile in situ precipitation method for preparing a non-peripheral octamethyl-substituted cobalt(II)phthalocyanine (N-CoMePc)/reduced graphene oxide (rGO) nanocomposite as an efficient photocatalyst. The physical and chemical properties of the nanocomposite were investigated by scanning electron microscopy, transmission electron microscopy, x-ray diffraction, and ultraviolet-visible, ultraviolet photoelectron, Fourier-transform infrared, Raman, and x-ray photoelectron spectroscopies.

Molecular Design Strategy in Developing Titanyl Phthalocyanines as Dopant-Free Hole-Transporting Materials for Perovskite Solar Cells: Peripheral or Nonperipheral Substituents?

We demonstrate a molecular design strategy to enhance the efficiency of phthalocyanine (Pc)-based hole-transporting materials (HTMs) in perovskite solar cells (PSCs). Herein, two titanyl phthalocyanine (TiOPc) derivatives are designed and applied as dopant-free HTMs in planar n-i-p-structured PSCs. The newly developed TiOPc compounds possess eight -hexylthio groups attached to either peripheral (-SC-TiOPc) or nonperipheral (-SC-TiOPc) positions of the Pc ring.