Since the discovery of graphene, two-dimensional ultrathin nanomaterials with an atomic thickness (typically <5 nm) have attracted tremendous interest due to their fascinating chemical and physical properties. These ultrathin nanomaterials, referred to as atomically thin materials (ATMs), possess inherent advantages such as a high specific area, highly exposed surface-active sites, efficient atom utilization, and unique electronic structures. While substantial efforts have been devoted to advancing ATMs through structural chemistry, the potential of heterointerface engineering to enhance their properties has not yet been fully recognized. Indeed, the introduction of bi- or multi-components to construct a heterointerface has emerged as a crucial strategy to overcome the limitations in property enhancement during ATM design. In this review, we aim to summarize the design principles of heterointerfacial ATMs, present general strategies for manipulating their interfacial structure and catalytic properties, and provide an overview of their application in energy conversion and storage, including the hydrogen evolution reaction (HER), the oxygen evolution reaction (OER), the oxygen reduction reaction (ORR), the CO electroreduction reaction (CORR), photocatalysis, and rechargeable batteries. The central theme of this review is to establish correlations among interfacial modulation, structural and electronic properties, and ATMs' major applications. Finally, based on the current research progress, we propose future directions that remain unexplored in interfacial ATMs for enhancing their properties and introducing novel functionalities in practical applications.
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http://dx.doi.org/10.3390/ma16175829 | DOI Listing |
Nanotechnology
March 2025
Department of Chemistry, Jamia Millia Islamia, New Delhi-110025, New Delhi, Delhi, 110025, INDIA.
One compelling goal of carbon-neutrality is to advance sustainable energy applications through advanced functional nanomaterials for achieving remarkable performance in energy conversion processes, especially in green H2 energy. Here, Ag-modified TiO2 nanostructures with highly specific exposed surface sites have been fabricated hydrothermally, elucidating its prominence towards photocatalytic, and photo/-electrocatalytic H2 production. Further, the as-synthesized nanomaterials were investigated by XRD, electron microscopy (SEM/EDAX/TEM/HRTEM), ICP-MS, PL, Raman, UV-visible DRS, and BET surface area studies.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
February 2025
College of Chemistry and Materials Science, Jinan University, Guangzhou, 510632, P.R. China.
To advance electrochemical HO production and unravel catalytic mechanisms, the precise structural coordination of single-atomic M-N-C electrocatalysts is urgently required. Herein, the Co─N site with an asymmetric electronic configuration is constructed to boost the two-electron oxygen reduction reaction (2e ORR) compared to symmetric Co─N, effectively overcoming the trade-off between activity and selectivity in HO production. Both experimental and theoretical analyses demonstrate that breaking the symmetry of Co─N sites promotes the activation of O molecules and moderates the adsorption of the key *OOH intermediate by disrupting the linear scaling relationship for intermediates adsorption.
View Article and Find Full Text PDFAnal Chim Acta
March 2025
Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Bioinorganic Chemistry & Materia Medica, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Luoyu Road 1037, Wuhan, 430074, China. Electronic address:
Background: Self-powered electrochemical sensors derived from photofuel cells (PFCs) have emerged as a promising analytical tool due to their simplicity and low energy requirements. Nevertheless, the limited photoelectric response of photoelectrode often does not generate adequate output power for effective sensor application. This study addresses this critical issue by exploring innovative strategies to enhance the photoelectric performance of BiVO photoanodes.
View Article and Find Full Text PDFDalton Trans
February 2025
School of Chemistry and Chemical Engineering, Guangdong Provincial Key Laboratory of Fuel Cell Technology, South China University of Technology, Guangzhou 510641, P.R. China.
A series of antimony(III) triaryl corroles bearing different numbers of -pentafluorophenyl substituents was synthesized and evaluated as catalysts for electrocatalytic hydrogen evolution. Introduction of the electron-withdrawing pentafluorophenyl group to the corrole macrocycle led to a significant boost in electro-catalytic hydrogen evolution reaction (HER) activity in organic and aqueous media, highlighting the tunability of these complexes for enhanced catalytic activity.
View Article and Find Full Text PDFNanomicro Lett
February 2025
State Key Laboratory of Precision Spectroscopy, Engineering Research Center of Nanophotonics and Advanced Instrument (Ministry of Education), School of Physics and Electronic Science, East China Normal University, Shanghai, 200241, People's Republic of China.
The coupling of fast redox kinetics, high-energy density, and prolonged lifespan is a permanent aspiration for aqueous rechargeable zinc batteries, but which has been severely hampered by a narrow voltage range and suboptimal compatibility between the electrolytes and electrodes. Here, we unprecedentedly introduced an electric ambipolar effect for synergistic manipulation on Zn ternary-hydrated eutectic electrolyte (ZTE) enabling high-performance Zn-Br batteries. The electric ambipolar effect motivates strong dipole interactions among hydrated perchlorates and bipolar ligands of L-carnitine (L-CN) and sulfamide, which reorganized primary cations solvation sheath in a manner of forming Zn[(L-CN)(SA)(HO)] configuration and dynamically restricting desolvated HO molecules, thus ensuring a broadened electrochemical window of 2.
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