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Tuning the electronic metal-carbon interactions in Lignin-based carbon-supported ruthenium-based electrocatalysts for enhanced hydrogen evolution reactions.
- Source :
-
Journal of Colloid & Interface Science . Jun2024, Vol. 664, p251-262. 12p. - Publication Year :
- 2024
-
Abstract
- [Display omitted] • A valorisation route for sodium lignosulfonate to fabricate electrocatalysts based on N/S- co -doped Ruthenium for HER is showcased. • The effect of S defects on the electronics metal-carbon interactions (EMICs) between Ruthenium and carbon supports is studied in-depth. • The high HER activity tailoring by enhanced EMICs is further revealed by electrochemical testing and density functional theory (DFT) computations. Ruthenium (Ru) nanoparticles dispersed on carbon support are promising electrocatalysts for hydrogen evolution reaction (HER) due to strong electronic metal-carbon interactions (EMCIs). Defects engineering in carbon supports is an effective strategy to adjust EMCIs. We prepared nitrogen/sulfur co-doped carbon supported Ru nanoparticles (Ru@N/S-LC) using sodium lignosulfonate and urea as feedstocks. Intrinsic S dopants from sodium lignosulfonate create rich S defects, thus enhancing the EMCIs within Ru@N/S-LC, leading a faster electron transfer between Ru nanoparticles and N/S-LC compared with N -doped carbon supported Ru nanoparticles (Ru@ N -CC). The resulting Ru@N/S-LC exhibits an enhanced work function and a down-shifted d-band center, inducing stronger electron capturing ability and weaker hydrogen desorption energy than Ru@ N -CC. Ru@N/S-LC requires only 7 and 94 mV overpotential in acidic medium and alkaline medium to achieve a current density of 10 mA cm−2. Density Functional Theory (DFT) calculations were utilized to clarify the impact of sulfur (S) doping and the mechanism underlying the notable catalytic activity of Ru@N/S-LC. This study offers a perspective for utilizing the natural dopants of biomass to adjust the EMCIs for electrocatalysts. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00219797
- Volume :
- 664
- Database :
- Academic Search Index
- Journal :
- Journal of Colloid & Interface Science
- Publication Type :
- Academic Journal
- Accession number :
- 176390961
- Full Text :
- https://doi.org/10.1016/j.jcis.2024.03.019