98%
921
2 minutes
20
Electrochemical CO reduction reaction (CO RR) is a promising approach to convert CO to carbon-neutral fuels using external electric powers. Here, the Bi S -Bi O nanosheets possessing substantial interface being exposed between the connection of Bi S and Bi O are prepared and subsequently demonstrate to improve CO RR performance. The electrocatalyst shows formate Faradaic efficiency (FE) of over 90% in a wide potential window. A high partial current density of about 200 mA cm at -1.1 V and an ultralow onset potential with formate FE of 90% are achieved in a flow cell. The excellent electrocatalytic activity is attributed to the fast-interfacial charge transfer induced by the electronic interaction at the interface, the increased number of active sites, and the improved CO adsorption ability. These collectively contribute to the faster reaction kinetics and improved selectivity and consequently, guarantee the superb CO RR performance. This study provides an appealing strategy for the rational design of electrocatalysts to enhance catalytic performance by improving the charge transfer ability through constructing a functional heterostructure, which enables interface engineering toward more efficient CO RR.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/smll.202105682 | DOI Listing |
Org Lett
September 2025
Department of Chemistry, Indian Institute of Techology Bombay, Powai, Mumbai 400076, India.
The direct α-α coupling of 3-pyrrolyl boron dipyrromethenes (BODIPYs) affords helical near-infrared (NIR)-active dimers in one step via a radical Pd-catalyzed process. X-ray analysis reveals Z-type helical packing stabilized by π-π stacking and hydrogen-bonding interactions. These dimers showed pronounced bathochromic absorption shifts compared to monomers and solvent-dependent charge-transfer bands up to 905 nm with fluorescence quenching.
View Article and Find Full Text PDFNano Lett
September 2025
Department of Physics, Columbia University, New York, New York 10027, United States.
Graphene-based photonic structures have emerged as fertile ground for the controlled manipulation of surface plasmon polaritons (SPPs), providing a two-dimensional platform with low optoelectronic losses. In principle, nanostructuring graphene can enable further confinement of nanolight─enhancing light-matter interactions in the form of SPP cavity modes. In this study, we engineer nanoscale plasmonic cavities composed of self-assembled C arrays on graphene.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Tianjin Key Laboratory of Film Electronic & Communicate Devices, School of Integrated Circuit Science and Engineering, Tianjin University of Technology, Tianjin 300384, China.
Owing to their distinctive thickness and physical attributes, two-dimensional (2D) materials have exhibited considerable promise in the field of microelectronic devices. Notably, 2D magnetic materials that maintain long-range magnetic order and can be readily modulated by external fields have garnered substantial attention. However, CrSBr, despite being a 2D van der Waals (vdW) semiconducting magnet with an appropriate band gap and stability in air, faces significant hindrance for practical utilization due to its Curie temperature () of 146 K.
View Article and Find Full Text PDFSmall Methods
September 2025
Department of Materials Science and Engineering, National Cheng Kung University, No. 1 University Road, Tainan, 70101, Taiwan.
Electron Fenton (EF) degradation often suffers from low in situ HO electrosynthesis and Fe regeneration. Herein, a novel multi-element oxide-sulfide heterostructure is reported, (FeVCoCuMn)O/(CuFeVCoMn)S, for efficient and stable EF degradation. The oxide-sulfide phase ratio is optimized through temperature control during the synthesis.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Beijing Advanced Innovation Center for Soft Matter Science and Engineering & State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, 100029, P.R. China.
The donor/acceptor (D/A) interfaces in bulk heterojunction (BHJ) organic solar cells (OSCs) critically govern exciton dissociation and molecular diffusion, determining both efficiency and stability. Herein, we design a double-cable conjugated polymer, SC-1F, to insert into a physically-blended D/A system to optimize the interface. We have found that SC-1F spontaneously segregates to the interface through favorable miscibility and heterogeneous nucleation with the acceptor.
View Article and Find Full Text PDF