The success of the rational bottom-up approach to nanostructured carbon materials and the discovery of the importance of their doping with heteroatoms puts under the spotlight all synthetic organic approaches to polycyclic aromatic hydrocarbons. The construction of atomically precise heteroatom doped nanographenes has evidenced the importance of controlling its geometry and the position of the doping heteroatoms, since these parameters influence their chemical-physical properties and their applications. The growing interest towards this research topic is testified by the large number of works published in this area, which have transformed a once "fundamental research" into applied research at the cutting edge of technology. This review analyzes the most recent synthetic approaches to this class of compounds.
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http://dx.doi.org/10.3390/molecules26206306 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Sichuan University, Institute of New Energy and Low-Carbon Technology, CHINA.
Doping with non-metallic heteroatom is an effective approach to tailor the electronic structure of Ni for enhancing its alkaline hydrogen oxidation reaction (HOR) catalytic performance. However, the modulation of HOR activity of Ni by lattice carbon (LC) atoms has rarely been reported, especially to reveal the rule between the doping effect and activity caused by the content of LC atoms. Here, hydrogen is proposed as a scavenger for LC atoms in the pyrolytic reduction process to finely control the content of LC atoms in Ni.
View Article and Find Full Text PDFACS Mater Au
January 2025
Department of Chemistry, University of Rochester, Rochester, New York 14627, United States.
The utilization of polyoxometalate-based materials is largely dictated by their redox properties. Detailed understanding of the thermodynamic and kinetic efficiency of charge transfer is therefore essential to the development of polyoxometalate-based systems for target applications. Toward this end, we report electrochemical studies of a series of heteroatom-doped Keggin-type polyoxotungstate clusters [PWO] ( ), [VWO] ( ), [P(VW)O] ( ), and [V(VW)O] ( ) to elucidate the role of the identity and spatial location of heteroatoms and overall cluster charge on the rate constants of electron transfer and redox reaction entropies.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore.
Transition-metal dichalcogenides (TMDs), such as molybdenum disulfide (MoS), have emerged as a generation of nonprecious catalysts for the hydrogen evolution reaction (HER), largely due to their theoretical hydrogen adsorption energy close to that of platinum. However, efforts to activate the basal planes of TMDs have primarily centered around strategies such as introducing numerous atomic vacancies, creating vacancy-heteroatom complexes, or applying significant strain, especially for acidic media. These approaches, while potentially effective, present substantial challenges in practical large-scale deployment.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Chemistry and Research Institute for Natural Sciences, Korea University, Seoul, Republic of Korea.
The success of proton exchange membrane water electrolysis (PEMWE) depends on active and robust electrocatalysts to facilitate oxygen evolution reaction (OER). Heteroatom-doped-RuO has emerged as a promising electrocatalysts because heteroatoms suppress lattice oxygen participation in the OER, thereby preventing the destabilization of surface Ru and catalyst degradation. However, identifying suitable heteroatoms and achieving their atomic-scale coupling with Ru atoms are nontrivial tasks.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
School of Materials and Chemistry, Anhui Agricultural University, Hefei, Anhui 230036, China; Key Laboratory of Clean Dyeing and Finishing Technology of Zhejiang Province, Shaoxing, Zhejiang 312000, China. Electronic address:
Rational design of carbon material structures is essential for enhancing the performance of persulfate-based advanced oxidation processes (PS-AOPs) in water purification. In this study, a self-doping and self-templating strategy was devised to produce N, S co-doped biochar catalysts through pre-cryocrushing and carbonization procedures employing chitosan (N-source) and lignosulfonate (S-source) derived from biomass waste. The as-synthesized materials exhibited excellent performance in removing tetracycline (TC) through a synergistic process of adsorption and catalytic activation.
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