In-depth research on energy storage and conversion is urgently needed; thus, water splitting has become a possible method to achieve sustainable energy utilization. However, traditional carbon material with high graphitization degree exhibits a relatively low electrocatalytic oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) activity as it is electrochemically inert. In this work, according to the Lewis theory of acids and bases and the density functional theory (DFT) results, which show that the enriched heteroatom of B/N in the boron carbonitride (BCN) system may introduce stronger adsorption strength of OH*/HO, respectively, we have designed and synthesized self-supporting BCN materials with different enrichment degrees of B/N (B-BCN/N-BCN) using carbon paper as substrate. Furthermore, by adjusting the contents of B and N, the optimum electrocatalytic performance of overall water splitting was obtained in which the onset voltage of water splitting on B-BCN//N-BCN was lower than 1.60 V. Our strategy of synthesizing materials with different heteroatom enrichment to improve the electronic environment of materials has opened up new opportunities for developing efficient metal-free electrocatalysts.
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http://dx.doi.org/10.1039/d0nr06857h | DOI Listing |
Langmuir
January 2025
Department of Chemistry, Bharathiar University, Coimbatore 641 046, India.
Developing nonprecious metal-based electrocatalysts with exceptional activity and durability for water electrolysis remains a significant challenge. Herein, we report a highly efficient bifunctional electrocatalyst composed of sulfur-doped vanadium metal-organic frameworks (S@V-MOF) integrated with multiwalled carbon nanotubes (MWCNTs) to promote the synergistic effect between S@V-MOF and MWCNTs and modulate the electronic structure of the catalyst, which eventually enhanced its electrocatalytic performance. The S@V-MOF/MWCNT catalyst loaded at the Ni foam electrode exhibits remarkable activity for both the hydrogen evolution reaction (HER) in acidic media and oxygen evolution reaction (OER) in alkaline media, requiring overpotentials of 48 and 227 mV, respectively, to reach a current density of 10 mA cm.
View Article and Find Full Text PDFSmall
January 2025
UMR 8182, CNRS, Institut de Chimie Moléculaires et des Matériaux d'Orsay, Université Paris-Saclay, Orsay, 91405, France.
Capturing sunlight to fuel the water splitting reaction (WSR) into O and H is the leitmotif of the research around artificial photosynthesis. Organic semiconductors have now joined the quorum of materials currently dominated by inorganic oxides, where for both families of compounds the bandgaps and energies can be adjusted synthetically to perform the Water Splitting Reaction. However, elaborated and tedious synthetic pathways are necessary to optimize the photophysical properties of organic semiconductors.
View Article and Find Full Text PDFChemSusChem
January 2025
Sun Yat-Sen University, School of Materials Science and Engineering, No. 135, Xingang Xi Road, China, 510006, Guangzhou, CHINA.
Sluggish oxygen evolution reaction (OER) is a crucial part of water splitting and solar fuel generation, which limits their utilization. Ni3S2 is a promising OER catalyst, in which surface reconstruction is an important step to improve performance. In this study, DFT calculations were employed to investigate the effect of surface reconstruction on (001), (110), and (101) surfaces of Ni3S2 in alkaline OER.
View Article and Find Full Text PDFAdv Sci (Weinh)
January 2025
Computational Science Research Center, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea.
Efficiently extracting data from tables in the scientific literature is pivotal for building large-scale databases. However, the tables reported in materials science papers exist in highly diverse forms; thus, rule-based extractions are an ineffective approach. To overcome this challenge, the study presents MaTableGPT, which is a GPT-based table data extractor from the materials science literature.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Guangdong University of Technology - University Town Campus: Guangdong University of Technology, Applied Chemistry, 100 Waihuan West Road, 510006, Guangzhou, CHINA.
Expanding the spectral response of photocatalysts to facilitate overall water splitting (OWS) represents an effective approach for improving solar spectrum utilization efficiency. However, the majority of single-phase photocatalysts designed for OWS primarily respond to the ultraviolet region, which accounts for a small proportion of sunlight. Herein, we present a versatile strategy to achieve broad visible-light-responsive OWS photocatalysis dominated by direct ligand-to-cluster charge transfer (LCCT) within metal-organic frameworks (MOFs).
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