Tuning surface phosphorus chemistry in metal-free carbon electrocatalysts for enhanced hydrogen evolution
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Le résumé fourni par la source
The precise modulation of phosphorus species and physicochemical properties in metal-free carbon materials holds significant potential for enhancing their electrocatalytic performance in the hydrogen evolution reaction (HER). In this study, we precisely tune the phosphorus species during the pyrolysis of phytic acid (PA). Pluronic® F127 acts as a protective agent, preventing the close proximity of phosphorus groups in PA molecules during pyrolysis. This interaction inhibits the formation of polyphosphoric groups during carbonization and leads instead to isolated P functionalities embedded in carbon basal planes. Comprehensive characterization, including cross-polarization magic angle spinning solid-state 31 P-NMR, XPS, and DFT simulations identified the phosphorus species and elucidated their structural and electronic properties. The precise tuning of phosphorous functional groups enabled by Pluronic® F127 in metal-free carbon materials boosting the phosphorous based state-of-the-art HER catalytic performance. These findings underscore the underexplored potential of surfactants beyond morphological templating, offering a powerful strategy for tailoring surface chemistry and advancing the design of next-generation metal-free electrocatalysts. • Pluronic® F127 prevents phosphorus aggregation, enabling isolated P sites. • Surfactants modulate phosphorus species, enhancing HER electrocatalysis. • P-doped carbon catalyst achieves -0.19 V vs. RHE, rivaling metal-based HER. • Study paves the way for metal-free catalysts in sustainable hydrogen production.
Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.
Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Tuning surface phosphorus chemistry in metal-free carbon electrocatalysts for enhanced hydrogen evolution
- Date Crossref
- 01/04/2026
- Éditeur
- Elsevier BV
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
Les institutions déclarées
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