| 1. |
- Chen, X. X., et al.
(författare)
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Traditional earth-abundant coal as new energy materials to catalyze the oxygen reduction reaction in alkaline solution
- 2016
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Ingår i: Electrochimica Acta. - : Elsevier BV. - 0013-4686. ; 211, s. 568-575
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Tidskriftsartikel (refereegranskat)abstract
- Coal is an earth-abundant energy resource, however, its direct combustion results in serious environmental pollution. Therefore, it becomes important to design value-added products from coal and to maximize its value chain. Herein, brown coal was used to develop non-precious metal catalysts for the oxygen reduction reaction (ORR) in fuel cells as green energy conversion systems. The brown coal was first pretreated with different acids, followed by N-doping at 800 degrees C in a stream of NH3. A trace amount of Fe was further added to improve the electrocatalytic performance of the prepared catalyst towards ORR. The prepared coal-derived N-doped carbon further modified with 0.5% Fe exhibited onset potential of 0.92 V vs. RHE at a current density of -0.1 mA cm(-2) and a predominantly 4-electron transfer pathway of oxygen to water in 0.1 M NaOH, which was evaluated by RDE and RRDE. The prepared electrocatalysts were further characterized by elemental analysis, XRD, Raman and XPS. The results suggest that the coal-derived ORR catalyst have convoluted graphitic and amorphous carbon structures. The N-content increased after acid-pretreatment and subsequent functionalization with nitrogen, while it slightly decreased after Fe incorporation apparently due to coordination of Fe with N. ORR activity enhancement after the incorporation of Fe is expected to mainly arise from a synergetic effect involving the interaction of Fe with N groups distributed in the carbon matrix. (C) 2016 Elsevier Ltd. All rights reserved.
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| 2. |
- Xie, Kunpeng, 1985, et al.
(författare)
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Promoting effect of nitrogen doping on carbon nanotube-supported RuO2 applied in the electrocatalytic oxygen evolution reaction
- 2016
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Ingår i: Journal of Energy Chemistry. - : Elsevier BV. - 2095-4956. ; 25:2, s. 282-288
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Tidskriftsartikel (refereegranskat)abstract
- RuO2 nanoparticles supported on multi-walled carbon nanotubes (CNTs) functionalized with oxygen (OCNTs) and nitrogen (NCNTs) were employed for the oxygen evolution reaction (OER) in 0.1 M KOH. The catalysts were synthesized by metal-organic chemical vapor deposition using ruthenium carbonyl (Ru3(CO)12) as Ru precursor. The obtained RuO2/OCNT and RuO2/NCNT composites were characterized using TEM, H2-TPR, XRD and XPS in order probe structure-activity correlations, particularly, the effect of the different surface functional groups on the electrochemical OER performance. The electrocatalytic activity and stability of the catalysts with mean RuO2 particle sizes of 13-14 nm was evaluated by linear sweep voltammetry, cyclic voltammetry, and chronopotentiometry, showing that the generation of nitrogen-containing functional groups on CNTs was beneficial for both OER activity and stability. In the presence of RuO2, carbon corrosion was found to be significantly less severe.
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| 3. |
- Xie, Kunpeng, 1985, et al.
(författare)
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Room temperature synthesis of CdS nanoparticle-decorated TiO 2 nanotube arrays by electrodeposition with improved visible-light photoelectrochemical properties
- 2016
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Ingår i: Electrochemistry Communications. - : Elsevier BV. - 1388-2481. ; 63, s. 56-59
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Tidskriftsartikel (refereegranskat)abstract
- Controllable CdS nanoparticles (NPs) decorated on TiO2 nanotube arrays (NTAs) were prepared via electrodeposition in DMSO solution at room temperature, aiming to improve the photoelectrochemical properties of TiO2 NTA electrode in visible-light region. By tuning the concentrations of sulfur and Cd2+ as well as the deposition time, CdS NPs with different sizes can be controllably synthesized at room temperature. Excellent photocurrent response and incident photo to current conversion efficiency were achieved with smaller CdS NPs with optimal reactant concentrations and deposition time, which can be attributed to highly efficient charge separation and high dispersion of CdS NPs on both inner and outer surfaces of TiO2 nanotubes.
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