Coordination Chemistry Reviews, Journal Year: 2025, Volume and Issue: 534, P. 216603 - 216603
Published: March 7, 2025
Language: Английский
Coordination Chemistry Reviews, Journal Year: 2025, Volume and Issue: 534, P. 216603 - 216603
Published: March 7, 2025
Language: Английский
Applied Catalysis B Environment and Energy, Journal Year: 2024, Volume and Issue: 358, P. 124455 - 124455
Published: July 27, 2024
Language: Английский
Citations
10Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown
Published: June 10, 2024
Abstract Methanol‐electrooxidation‐reaction (MOR) to value‐added formate is a promising alternative water oxidation for cost‐efficient hydrogen production. It generally proposed that the MOR kinetics on Ni‐based catalysts are highly limited by transition rate of Ni(OH) 2 /NiOOH. Yet, how define catalyst following direct pathway without Ni 2+ /Ni 3+ remains challenging. Herein, core@shell heterostructured NiMoP x @Ni 5 P 4 developed selectively promote at large current density (> 500 mA cm −2 ). A series operando spectroscopic studies reveal negligible formation NiOOH with 1.0 m methanol in wide potential range, where predominant. Theoretical calculations demonstrate Ni‐P site favors adsorption * CH 3 OH over while heterostructure contributes significantly reduced energy barrier OCH → , hence promoting along NiOOH. Moreover, further study suggests also performs well toward cathodic evolution reaction (HER). As result, an electrode pair //NiMoP employed enable concurrent MOR/HER electrolysis 1.81 V yield formate/H FEs ca. 90/100% and long‐term (100‐h) sustainability under industrial conditions (6.0 KOH, 65 °C).
Language: Английский
Citations
9Journal of Energy Chemistry, Journal Year: 2024, Volume and Issue: 100, P. 234 - 244
Published: Aug. 30, 2024
Language: Английский
Citations
9Applied Catalysis B Environment and Energy, Journal Year: 2025, Volume and Issue: unknown, P. 125229 - 125229
Published: March 1, 2025
Language: Английский
Citations
1Journal of Energy Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 1, 2024
Language: Английский
Citations
8Journal of Material Science and Technology, Journal Year: 2024, Volume and Issue: 211, P. 123 - 133
Published: June 20, 2024
Language: Английский
Citations
7Rare Metals, Journal Year: 2024, Volume and Issue: unknown
Published: July 22, 2024
Language: Английский
Citations
7Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown
Published: Aug. 29, 2024
Abstract Ni phosphides and NiCo alloys are extensively explored for their remarkable efficiency in biomass alcohol oxidations, yet the underlying mechanisms remain inadequately understood. This study thoroughly elucidates roles of Ni, Co, P improving catalytic performance Ni‐Co‐P catalysts electrochemical conversion 5‐hydroxymethylfurfural (HMF) to 2,5‐furandicarboxylic acid (FDCA), a promising biomass‐derived building block replacing terephthalic acid. Phosphorization results partial formation 2 phase significantly boosts reactive NiOOH on surface, which is crucial converting HMF into FDCA. The integration Co heterojunction between enhances oxidation reactivity 5‐formyl‐2‐furancarboxylic (FFCA), pivotal intermediate influencing FDCA productivity, by selectively stabilizing aldehydes, thereby promoting further rather than surface desorption. situ /operando spectroscopic analyses consistently highlight equal significance rapid generation robust adsorption reactant molecules at achieving high performance. These insights elemental contributions set new standard designing multi‐component electrocatalysts efficient oxidation.
Language: Английский
Citations
7Chem, Journal Year: 2024, Volume and Issue: 10(9), P. 2666 - 2699
Published: Aug. 15, 2024
Language: Английский
Citations
6ACS Applied Nano Materials, Journal Year: 2024, Volume and Issue: 7(7), P. 7605 - 7613
Published: March 28, 2024
The electrooxidation of 5-hydroxymethylfurfural (HMF) provides a prospective method to produce high-value 2,5-furandicarboxylic acid (FDCA). Since this multistep process includes the oxidation aldehyde and hydroxyl groups, deep understanding mechanism HMF reaction (HMFOR) is crucial. Herein, surface reconstruction nickel-based catalyst regulated by Co V2O3 modifications reveal relationship between reconstructed HMFOR performance. introduction nanosheet facilitates in situ nanocatalyst enhancing adsorption OH*. incorporation adjusts electronic structure nickel, contributing decrease formation potential NiOOH. Moreover, insitugenerated NiOOH promotes activation providing beneficial effects for HMFOR. Impressively, Co–Ni/V2O3/NF needs only 1.29 VRHE achieve 10 mA cm–2 maintains high FDCA selectivity cycles. This work explains regulations on species formation, which conducive designing an efficient oxidation.
Language: Английский
Citations
5