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Methane (CH 4 ) oxidation to high value chemicals under mild conditions through photocatalysis is a sustainable and appealing pathway, nevertheless confronting the critical issues regarding both conversion and selectivity. Herein, under visible irradiation (420 nm), the synergy of palladium (Pd) atom cocatalyst and oxygen vacancies (OVs) on In 2 O 3 nanorods enables superior photocatalytic CH 4 activation by O 2 . The optimized catalyst reaches ca. 100 μmol h −1 of C1 oxygenates, with a selectivity of primary products (CH 3 OH and CH 3 OOH) up to 82.5%. Mechanism investigation elucidates that such superior photocatalysis is induced by the dedicated function of Pd single atoms and oxygen vacancies on boosting hole and electron transfer, respectively. O 2 is proven to be the only oxygen source for CH 3 OH production, while H 2 O acts as the promoter for efficient CH 4 activation through ·OH production and facilitates product desorption as indicated by DFT modeling. This work thus provides new understandings on simultaneous regulation of both activity and selectivity by the synergy of single atom cocatalysts and oxygen vacancies. CH4 oxidation to high value chemicals under mild conditions through photocatalysis confronts critical issues regarding both conversion and selectivity. Here, atomic Pd and oxygen vacancies were integrated on In2O3 nanorods, leading to visible-driven CH4 conversion with a remarkable yield of oxygenates and high selectivity of primary products.

To meet the requirements of potential applications, it is of great importance to explore new catalysts for formic acid oxidation that have both ultra-high mass activity and CO resistance. Here, we successfully synthesize atomically dispersed Rh on N-doped carbon (SA-Rh/CN) and discover that SA-Rh/CN exhibits promising electrocatalytic properties for formic acid oxidation. The mass activity shows 28- and 67-fold enhancements compared with state-of-the-art Pd/C and Pt/C, respectively, despite the low activity of Rh/C. Interestingly, SA-Rh/CN exhibits greatly enhanced tolerance to CO poisoning, and Rh atoms in SA-Rh/CN resist sintering after long-term testing, resulting in excellent catalytic stability. Density functional theory calculations suggest that the formate route is more favourable on SA-Rh/CN. According to calculations, the high barrier to produce CO, together with the relatively unfavourable binding with CO, contribute to its CO tolerance.Atomically dispersed Rh on N-doped carbon exhibits 28- and 67-fold enhancements compared with state-of-the-art Pd/C and Pt/C, despite the low activity of Rh/C. The Rh single atoms exhibit high tolerance to CO poisoning compared to Rh nanoparticles.

The selective hydrogenation of CO 2 to value-added chemicals is attractive but still challenged by the high-performance catalyst. In this work, we report that gallium nitride (GaN) catalyzes the direct hydrogenation of CO 2 to dimethyl ether (DME) with a CO-free selectivity of about 80%. The activity of GaN for the hydrogenation of CO 2 is much higher than that for the hydrogenation of CO although the product distribution is very similar. The steady-state and transient experimental results, spectroscopic studies, and density functional theory calculations rigorously reveal that DME is produced as the primary product via the methyl and formate intermediates, which are formed over different planes of GaN with similar activation energies. This essentially differs from the traditional DME synthesis via the methanol intermediate over a hybrid catalyst. The present work offers a different catalyst capable of the direct hydrogenation of CO 2 to DME and thus enriches the chemistry for CO 2 transformations. The conversion of CO 2 to valuable chemicals is still challenged by catalyst developments. Herein, the authors found that GaN is an efficient catalyst for selective CO 2 hydrogenation to dimethyl ether as the primary product, in contrast to the traditional methanol-intermediate route over hybrid catalysts.

Identification on catalytic sites of heterogeneous catalysts at atomic level is important to understand catalytic mechanism. Surface engineering on defects of metal oxides can construct new active sites and regulate catalytic activity and selectivity. Here we outline the strategy by controlling surface defects of nanoceria to create the solid frustrated Lewis pair (FLP) metal oxide for efficient hydrogenation of alkenes and alkynes. Porous nanorods of ceria ( PN -CeO 2 ) with a high concentration of surface defects construct new Lewis acidic sites by two adjacent surface Ce 3+ . The neighbouring surface lattice oxygen as Lewis base and constructed Lewis acid create solid FLP site due to the rigid lattice of ceria, which can easily dissociate H–H bond with low activation energy of 0.17 eV. Surface engineering of catalysts allows the tailoring of active sites. Here the authors produce a heterogeneous nanoceria catalyst with engineered defects producing active solid frustrated Lewis pair sites, and use these materials for the hydrogenation of alkynes and alkenes.

Despite significant advances in the fabrication and applications of graphene-like materials, it remains a challenge to prepare single-layered metallic materials, which have great potential applications in physics, chemistry and material science. Here we report the fabrication of poly(vinylpyrrolidone)-supported single-layered rhodium nanosheets using a facile solvothermal method. Atomic force microscope shows that the thickness of a rhodium nanosheet is <4 Å. Electron diffraction and X-ray absorption spectroscopy measurements suggest that the rhodium nanosheets are composed of planar single-atom-layered sheets of rhodium. Density functional theory studies reveal that the single-layered Rh nanosheet involves a δ-bonding framework, which stabilizes the single-layered structure together with the poly(vinylpyrrolidone) ligands. The poly(vinylpyrrolidone)-supported single-layered rhodium nanosheet represents a class of metallic two-dimensional structures that might inspire further fundamental advances in physics, chemistry and material science. Single-layered materials such as graphene are well known, but metallic elements tend to favour three-dimensional clusters. Here the authors report the synthesis of rhodium nanosheets—a supported, single-layered metallic material with rare δ-bonding.

Single-atom precious metal catalysts hold the promise of perfect atom utilization, yet control of their activity and stability remains challenging. Here we show that engineering the electronic structure of atomically dispersed Ru 1 on metal supports via compressive strain boosts the kinetically sluggish electrocatalytic oxygen evolution reaction (OER), and mitigates the degradation of Ru-based electrocatalysts in an acidic electrolyte. We construct a series of alloy-supported Ru 1 using different PtCu alloys through sequential acid etching and electrochemical leaching, and find a volcano relation between OER activity and the lattice constant of the PtCu alloys. Our best catalyst, Ru 1 –Pt 3 Cu, delivers 90 mV lower overpotential to reach a current density of 10 mA cm −2 , and an order of magnitude longer lifetime over that of commercial RuO 2 . Density functional theory investigations reveal that the compressive strain of the Pt skin shell engineers the electronic structure of the Ru 1 , allowing optimized binding of oxygen species and better resistance to over-oxidation and dissolution. While Ru-based electrocatalysts are among the most active for acidic water oxidation, they suffer from severe deactivation. Now, Yuen Wu, Wei-Xue Li and co-workers report a core–shell Ru 1 –Pt 3 Cu catalyst with surface-dispersed Ru atoms for a highly active and stable oxygen evolution reaction in acid electrolyte.

After stepping into the pandemic, it has been entirely not bizarre to wear facial masks to diminish the spreading of viruses in human daily outings. Due to the low expense and stable protection capability, disposable masks are the most widely used types of medical masks. By functionalities and medical standards, disposable masks mainly consist of surgical masks and N95/KN95 respirators in the market. In the assembling scheme, there are typically three or more polymeric layers (i.e., mainly polypropylene) in disposable masks; in addition, the ear loops in masks are usually made from textile constituents, such as polyamides. Therefore, the vast utilization and rapid accumulation of disposal mask waste can directly bring an emerging crisis of foreseeable environmental pollution. To minimize and prevent such mask-led microplastic pollution, chemical pyrolysis of mask waste is one of the most feasible and promising strategies. Via the direct and selective pyrolysis of disposable masks, it can effectively convert the mask waste into high-value fuel-range chemicals, e.g., liquid hydrocarbon blends, aromatics, C1–5 gas alkanes/alkenes, hydrogen, etc. In this way, it can not only tackle environmental challenges from plastic waste but also afford sustainable fuels with low carbon emission and circular economy.

We report a comprehensive theoretical investigation of the catalytic reaction mechanisms of propene epoxidation on gold nanoclusters using density functional theory （DFT）. We have shown that water acts as a catalytic promoter for propene epoxidation on gold catalysts. Even without reducible supports, hydroperoxyl （OOH） and hydroxyl （OH） radicals are readily formed on small-size gold clusters from co-adsorbed H20 and 02, with energy barriers as low as 4-6 kcal/mol （1 cal = 4.186 J）. Propene epoxidation occurs easily through reactions between C3H6 and the weakened O-O bond of the OOH radicals on the surfaces of gold clusters.

Activation of molecular O2 is the most critical step in gold-catalyzed oxidation reactions; however, the underlying mechanisms of this process remain under debate. In this study, we propose an alternative O2 activation pathway with the assistance of hydrogen-containing substrates using density functional theory. It is demonstrated that the co-adsorbed H-containing substrates （R-H） not only enhance the adsorption of O2, but also transfer a hydrogen atom to the adjacent O2, leading to O2 activation by its transformation to a hydroperoxyl （OOH） radical species. The activation barriers of the H-transfer from 16 selected R-H compounds （H2O, CH3OH, NH2CHCOOH, CH3CH=CH2, （CH3）2SiH2, etc.） to the co-adsorbed O2 are lower than 0.50 eV in most cases, indicating the feasibility of the activation of O2 via OOH under mild conditions. The formed OOH oxidant, with an increased O-O bond length of -1.45 A, either participates directly in oxidation reactions through the end-on oxygen atom, or dissociates into atomic oxygen and hydroxyl （OH） by crossing a fairly low energy barrier of 0.24 eV. Using CO oxidation as a probe, we have found that OOH has superior activity than activated O2 and atomic oxygen. This study reveals a new pathway for the activation of O2, and may provide insight into the oxidation catalysis of nanosized gold.

Methane-to-syngas conversion plays an important role in industrial gas-to-liquid technologies, which is commercially fulfilled by energy-intensive reforming methods. Here we present a highly selective and durable iron-based La 0.6 Sr 0.4 Fe 0.8 Al 0.2 O 3-δ oxygen carrier for syngas production via a solar-driven thermochemical process. It is found that a dynamic structural transformation between the perovskite phase and a Fe 0 @oxides core–shell composite occurs during redox cycling. The oxide shell, acting like a micro-membrane, avoids direct contact between methane and fresh iron(0), and prevents coke deposition. This core–shell intermediate is regenerated to the original perovskite structure either in oxygen or more importantly in H 2 O–CO 2 oxidant with simultaneous generation of another source of syngas. Doping with aluminium cations reduces the surface oxygen species, avoiding overoxidation of methane by decreasing oxygen vacancies in perovskite matrix. As a result, this material exhibits high stability with carbon monoxide selectivity above 95% and yielding an ideal syngas of H 2 /CO ratio of 2/1. Iron-based oxides are promising oxygen carriers for thermochemical syngas production, but can be prone to deactivation during the reaction. Here an iron-based catalyst is shown to transform reversibly between perovskite and core–shell structures during methane-to-syngas conversion, accounting for its high stability toward coke deposition.