Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 158785 - 158785
Опубликована: Дек. 1, 2024
Язык: Английский
Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 158785 - 158785
Опубликована: Дек. 1, 2024
Язык: Английский
Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 159810 - 159810
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
2Coordination Chemistry Reviews, Год журнала: 2025, Номер 529, С. 216468 - 216468
Опубликована: Янв. 21, 2025
Язык: Английский
Процитировано
2Journal of the American Chemical Society, Год журнала: 2025, Номер unknown
Опубликована: Янв. 6, 2025
Despite their enormous impact in modern heterogeneous catalysis, single-atom catalysts (SACs) continue to puzzle the catalysis community, which often struggles draw correct conclusions SAC-catalyzed experiments. In many cases, reasons for such an uncertainty originate from lack of knowledge exact evolution under operative conditions and fundamental factors controlling fate single atom relation catalytic mechanism. This has led confusion also about definition terminology, where coined term
Язык: Английский
Процитировано
1Molecular Catalysis, Год журнала: 2025, Номер 577, С. 114927 - 114927
Опубликована: Март 4, 2025
Язык: Английский
Процитировано
0Solar RRL, Год журнала: 2025, Номер unknown
Опубликована: Март 4, 2025
Single‐atom catalysts (SACs) show promise because of their efficient use precious metals, unique coordination and electronic structures, excellent tunability. Photocatalysis can harvest solar energy to drive energetically unfavorable reactions under mild conditions, offering a sustainable alternative energy‐intensive reactions. However, the efficiency photocatalysis is limited by poor spectrum utilization rapid charge recombination. Integrating single atoms into semiconductor photocatalysts promising route address these limitations. Mechanistic understanding single‐atom crucial for developing as they guide effective material design. This work provides an overview current knowledge on platinum group SACs applied photocatalytic applications with focus role in The review begins summary advantages metal well common structures. A concise synthesis methods then provided, followed comprehensive characterization SAC structure, photoelectronic properties, mechanisms action. Next, improving general processes specific are discussed. Finally, future outlooks development included further advancements field.
Язык: Английский
Процитировано
0Molecular Catalysis, Год журнала: 2025, Номер 578, С. 115017 - 115017
Опубликована: Март 11, 2025
Язык: Английский
Процитировано
0Small, Год журнала: 2025, Номер unknown
Опубликована: Март 21, 2025
Achieving a precise understanding and accurate design of heterogeneous catalysts based on bioinspired principles is challenging yet crucial to digging out optimal materials for artificial catalysis. Here, an ADH-mimicking dual-site photocatalyst (YCuCdS) developed, demonstrates the powerful effects atomic site configuration proton transfer environments alcohol-amine coupling. Mechanism studies reveal that alcohol substrate effectively dehydrogenated at Y sites, forming carbonyl intermediates rapidly experience condensation with amine. Meanwhile, released hydrogen species (Hads) migrate from adjacent Cu sites active S atoms, promoting H2 production hindering over-hydrogenation imine. As result, high imine yield 92% achieved, along rate 7400 µmol g-1 h-1. This work showcases effective strategy bioinspiration.
Язык: Английский
Процитировано
0Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 162016 - 162016
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0Nano Letters, Год журнала: 2025, Номер unknown
Опубликована: Апрель 14, 2025
Cocatalyst engineering is critical for advancing photocatalysis, as it suppresses charge carrier recombination, promotes interfacial electron/hole extraction, and serves active sites redox reactions. However, the incompatibility existing between cocatalyst host photocatalyst, along with its intrinsic properties of sites, limits further improvements in separation, surface reaction kinetics, overall performance. Herein, we introduce palladium hydrides (PdHx) an efficient on SrTiO3 (STO) photocatalytic water splitting, owing to their similar lattice parameters. The constructed PdHx/STO demonstrates a remarkable 6.4-fold enhancement hydrogen evolution compared Pd/STO control, reaching rate 5 mmol·g-1·h-1 at stoichiometric H2/O2 ratio 2:1. Structural characterizations theoretical analyses prove that situ formed PdHx feature advantages accelerated electron extraction modulated adsorption energies evolution; femtosecond transient absorption spectroscopy reveals prolonged lifetime improved transfer efficiency.
Язык: Английский
Процитировано
0Journal of Energy Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0