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- Khan, Safia, et al.
(författare)
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Kinetic and thermodynamic analysis of ammonia electro-oxidation over alumina supported copper oxide (CuO/Al2O3) catalysts for direct ammonia fuel cells
- 2024
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Ingår i: International journal of hydrogen energy. - : Elsevier. - 0360-3199 .- 1879-3487. ; 52, s. 1206-1216
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Tidskriftsartikel (refereegranskat)abstract
- In this work, ammonia electrooxidation (AEO) is studied to probe the electrochemical behavior of aqueous NH3 as direct fuel by implication of gamma alumina supported copper oxide catalysts (CuO/Al2O3). Precipitation and impregnation techniques are adapted to synthesize the substrate Al2O3, and loading of different ratios (1%, 2%, 3%, 4%) of active precursor i.e., CuO, respectively. Small average crystallite sizes (DAvg) in range of 1.46–6.76 nm and smaller particle sizes from micrographs proposed a superb activity of the catalysts. Modified GCE exhibited the excellent conductive properties towards standard redox probe K4[Fe(CN)6] and KCl, displaying a high active electrochemical surface area of up to 0.0021 cm2. Current profiles in response to increase in scan rates, concentrations of ammonia and temperature have been observed in 0.1 M KOH, thereby estimating the thermodynamic and kinetic constraints of the AEO process. Attributed to the electroactive properties towards AEO, CuO/Al2O3 is found to exhibit the desirable physiochemical properties owing to large oxidation current, large diffusion coefficient “D°” (3.6 × 10-9 cm2 s-1), large rate constant “ko” (1.2 × 10-5 cm s-1), large system entropy “ΔS” (-108 J K-1 mol-1), high change in enthalpy “ΔH” (72.3 J mol-1) and low activation energy “ΔG” (32.8 kJ mol-1). Resultingly, the oxidation of ammonia is found to be facile and robust by incorporation of CuO/Al2O3 catalysts owing to large ko, ΔH and ΔH. This study opened a gateway towards eco-benign and economical efficient energy generation and viable market entry of direct ammonia fuel cells.
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| 2. |
- Nasir, Mehwish Huma, et al.
(författare)
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Calcium-, magnesium-, and yttrium-doped lithium nickel phosphate nanomaterials as high-performance catalysts for electrochemical water oxidation reaction
- 2024
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Ingår i: Nanotechnology Reviews. - : Walter de Gruyter. - 2191-9089 .- 2191-9097. ; 13:1
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical water oxidation reaction (WOR) lies among the most forthcoming approaches toward eco-conscious manufacturing of green hydrogen owing to its environmental favors and high energy density values. Its vast commoditization is restricted by high-efficiency and inexpensive catalysts that are extensively under constant research. Herein, calcium, magnesium, and yttrium doped lithium nickel phosphate olivines (LiNi1-xMxPO, LNMP; x = 0.1-0.9; M = Ca2+, Mg2+, and Y3+) were synthesized via non-aqueous sol-gel method and explored for catalytic WOR. Lithium nickel phosphates (LNP) and compositions were characterized via Fourier transform infrared, scanning electron microscopy, X-ray diffraction, and energy dispersive X-ray diffraction techniques for the structural and morphological analyses. Glassy carbon electrode altered with the LNMPs when studied in a standard redox system of 5 mM KMnO4, displayed that yttrium doped LNP, i.e. LNYP-3 exhibits the highest active surface area (0.0050 cm(2)) displaying the lowest average crystallite size (D-avg) i.e. similar to 7 nm. Electrocatalytic behavior monitored in KOH showed that LNMP-2 offers the highest rate constant "k(o)," value, i.e. 3.9 10(-2) cm s(-1) and the largest diffusion coefficient "D-o," i.e. 5.2 x 10(-5) cm(2) s(-1). Kinetic and thermodynamic parameters demonstrated the facilitated electron transfer and electrocatalytic properties of proposed nanomaterials. Water oxidation peak current density values were indicative of the robust catalysis and facilitated water oxidation process besides lowering the Faradic onset potential signifying the transformation of less LNP into more conducive LNMP toward water oxidation.
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