Bioinspired N4-metallomacrocycles for electrocatalytic oxygen reduction reaction DOI
Yuliang Li, Ni Wang, Haitao Lei

et al.

Coordination Chemistry Reviews, Journal Year: 2021, Volume and Issue: 442, P. 213996 - 213996

Published: May 13, 2021

Language: Английский

Artificial spherical chromatophore nanomicelles for selective CO2 reduction in water DOI
Junlai Yu, Libei Huang,

Qingxuan Tang

et al.

Nature Catalysis, Journal Year: 2023, Volume and Issue: 6(6), P. 464 - 475

Published: May 18, 2023

Language: Английский

Citations

56

Efficient Photocatalytic CO2 Reduction in Ellagic Acid–Based Covalent Organic Frameworks DOI

Wan Lin,

Fu‐Wen Lin,

Jing Lin

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(23), P. 16229 - 16236

Published: May 30, 2024

Employing covalent organic frameworks (COFs) for the photocatalytic CO2 reduction reaction (CDRR) to generate high-value chemical fuels and mitigate greenhouse gas emissions represents a sustainable catalytic conversion approach. However, achieving superior CDRR performance is hindered by challenges of low charge separation efficiency, poor stability, high preparation costs associated with COFs. Herein, in this work, we utilized perfluorinated metallophthalocyanine (MPcF16) biomolecule compound ellagic acid (EA) as building blocks actualize functional named EPM-COF (M = Co, Ni, Cu). The designed EPCo-COF, featuring cobalt metal active sites, demonstrated an impressive CO production rate selectivity (CDRR). Moreover, following alkaline treatment (EPCo-COF-AT), COF exposed carboxylic anion (COO–) hydroxyl group (OH), thereby enhancing electron-donating capability EA. This modification achieved heightened 17.7 mmol g–1 h–1 outstanding 97.8% efficient CDRR. Theoretical calculations further illustrated that EPCo-COF-AT functionalized COO– OH can effectively alleviate energy barriers involved process, which facilitates proton-coupled electron transfer processes enhances on sites within EPCo-COF-AT.

Language: Английский

Citations

38

Ligand-Bound CO2 as a Nonclassical Route toward Efficient Photocatalytic CO2 Reduction with a Ni N-Confused Porphyrin DOI

Huihong Yuan,

Akash Krishna,

Zhihe Wei

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(15), P. 10550 - 10558

Published: April 8, 2024

Implementing the synergistic effects between metal and ligand has successfully streamlined energetics for CO2 activation gained high catalytic activities, establishing important breakthroughs in photocatalytic reduction. Herein, we describe a Ni(II) N-confused porphyrin complex (NiNCP) featuring an acidic N–H group. It is readily deprotonated exists anion form during catalysis. Owing to this functional site, NiNCP gave rise outstanding turnover number (TON) as 217,000 with 98% selectivity reduction CO, while parent (NiTPP) was found be nearly inactive. Our mechanistic analysis revealed nonclassical reaction pattern where effectively activated via attack of Lewis-basic ligand. The resulting ligand-bound adduct could further reduced produce CO. This new metal–ligand effect anticipated inspire design highly active catalysts small molecule activations.

Language: Английский

Citations

22

Identifying a highly efficient molecular photocatalytic CO2 reduction system via descriptor-based high-throughput screening DOI
Yangguang Hu, Can Yu, Song Wang

et al.

Nature Catalysis, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 7, 2025

Language: Английский

Citations

4

Bioinspired N4-metallomacrocycles for electrocatalytic oxygen reduction reaction DOI
Yuliang Li, Ni Wang, Haitao Lei

et al.

Coordination Chemistry Reviews, Journal Year: 2021, Volume and Issue: 442, P. 213996 - 213996

Published: May 13, 2021

Language: Английский

Citations

90