Repozitorij Univerze v Novi Gorici

Iskanje po repozitoriju
A+ | A- | Pomoč | SLO | ENG

Iskalni niz: išči po
išči po
išči po
išči po
* po starem in bolonjskem študiju

Opcije:
  Ponastavi


1 - 4 / 4
Na začetekNa prejšnjo stran1Na naslednjo stranNa konec
1.
An in situ proton filter covalent organic framework catalyst for highly efficient aqueous electrochemical ammonia production
Kayaramkodath C. Ranjeesh, Sukhjot Kaur, Abdul K. Mohammed, Safa Gaber, Divyani Gupta, Khaled Badawy, Mohamed Aslam, Nirpendra Singh, Tina Škorjanc, Matjaž Finšgar, 2023, izvirni znanstveni članek

Opis: The electrocatalytic nitrogen reduction reaction (NRR) driven by renewable electricity provides a green synthesis route for ammonia (NH3) production under ambient conditions but suffers from a low conversion yield and poor Faradaic efficiency (F.E.) because of strong competition from hydrogen evolution reaction (HER) and the poor solubility of N2 in aqueous systems. Herein, an in situ proton filter covalent organic framework catalyst (Ru-Tta-Dfp) is reported with inherent Ruthenium (Ru) sites where the framework controls reactant diffusion by suppressing proton supply and enhancing N2 flux, causing highly selective and efficient catalysis. The smart catalyst design results in a remarkable ammonia production yield rate of 2.03 mg h−1 mgcat−1 with an excellent F.E. of ≈52.9%. The findings are further endorsed with the help of molecular dynamics simulations and control COF systems without in situ proton filter feasibility. The results point to a paradigm shift in engineering high-performance NRR electrocatalysts for more feasible green NH3 production.
Ključne besede: covalent organic frameworks, ammonia, electrochemical synthesis, electrochemistry, nitrogen reduction reaction, ruthenium
Objavljeno v RUNG: 11.12.2023; Ogledov: 679; Prenosov: 6
.pdf Celotno besedilo (2,77 MB)
Gradivo ima več datotek! Več...

2.
3.
Metal hydroxides for energy conversion and energy storage
Andraž Mavrič, predavanje na tuji univerzi

Opis: Electrocatalysts, electrochromic devices, and pseudo-capacitors based on transition metal (oxy)hydroxides depend on the reversibility of the reduction-oxidation process of metal cations. Rapid switching between different redox states is often involved, particularly in electrocatalysis where redox metal sites act as active centers for electron transfer to the reactant. To ensure long-term durability, the reversibility of the redox metal sites should be robust. Nickel hydroxide is a model catalyst for the oxygen evolution reaction (OER) and the basic representative of the layered double hydroxides. It is frequently combined with other transition metals (e.g. Fe, Co, Mn), forming some of the most active OER electrocatalysts in alkaline media. [1] I will present the use of in-situ spectroscopy to track the reversibility of redox states of the Ni(OH)2 during its lifetime. During the operation at 200 mA cm-2 in 1 M KOH electrolyte, the catalytic activity of Ni(OH)2 gradually degrades until lastly, the catalyst breaks down. During the catalyst lifetime, the reduction-oxidation reversibility of the Ni2+/3+ redox couple is lost and the catalyst converts into an inactive phase. The reversibility of the redox couple is monitored by the in-situ UV/Vis spectroscopy. During the catalyst lifetime, the reversibility of the redox peak is lost. The activity collapse is attributed to the structural amorphization/disordering of the layered Ni(OH)2 catalyst, as confirmed by TEM investigations and in-situ Raman spectroscopy. [2] Similarly, the redox reversibility of metal sites is also important for long cycle life in supercapacitors, based on the pseudo-capacitance mechanism. Contrary to catalysts, for supercapacitors, the water oxidation needs to be suppressed to increase the working voltage range. I will discuss the mechanisms for the deactivation of transition metal hydroxides to serve as capacitors and approaches to increase power density. Finally, I will discuss the use of mixed metal hydroxides to serve as precursors for a copper oxide-based catalytic system for CO2 hydrogenation to methanol. Thermal decomposition of hydrotalcite-based hydroxide precursor is followed by in-situ x-ray diffraction. The conditions to prepare disordered oxide in contact with catalytical active Cu metal are identified and the catalytic performance of catalysts with crystalline and disordered oxide phases are compared. [1] A. Mavrič, C. Cui, (2021), Advances and Challenges in Industrial-Scale Water Oxidation on Layered Double Hydroxides, ACS Appl. Energy Mater., 4, 12032-12055. [2] A. Mavrič, M. Fanetti, Y. Lin, M. Valant, C. Cui, (2020), Spectroelectrochemical Tracking of Nickel Hydroxide Reveals Its Irreversible Redox States upon Operation at High Current Density, ACS Catal., 10, 9451-9457.
Ključne besede: electrochemistry, energy storage, CO2 hydrogenation, methnaol
Objavljeno v RUNG: 13.10.2022; Ogledov: 1323; Prenosov: 0
Gradivo ima več datotek! Več...

4.
Iskanje izvedeno v 0.03 sek.
Na vrh