Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain
the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in
Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles
and JavaScript.
Catalysis lies at the heart of the chemical industry. It encompasses heterogeneous catalysis, homogeneous catalysis and biocatalysis. This page showcases our recent publications that report cutting edge research across the field of catalysis.
Achieving high NH3 selective catalytic reduction activity at ultra-low temperatures (below 150 °C) remains a challenge for V-based catalysts. Here the authors explore the electron scissors effect of current-assisted catalysis, which enables a monoatomic V-based catalyst to exhibit exceptional denitration performance at ultra-low temperatures.
Unveiling the regulatory mechanism of regioselectivity in hydroformylation has been a significant challenge. Here the authors successfully demonstrate how hemilabile coordination influences regioselectivity by employing various in situ techniques.
Incorporating immiscible metals in high-entropy oxides creates unique catalytic sites but results in low specific surface areas due to the high formation temperature. Here the authors report low temperature synthesis of periodically aligned high-entropy LaMnO3 oxides and polyoxometalate heterostructures for photoelectrochemical coupling of methane into acetic acid under mild conditions.
The buried interface beneath the solid-liquid junction is crucial for photoelectrochemical device efficiency and requires precise characterization for optimization. Here the authors probe the in situ transformation of a CuxO interlayer at the NiO/n-Si interface by hard X-ray photoelectron spectroscopy and improve solar-to-hydrogen efficiency to 4.56%.
A strategy of covalently grafting molecular catalysts to polymer backbones in polymer dots photocatalysts is proposed in this work, realizing a groundbreaking photocatalytic oxidation of various alcohols in neutral conditions.
Developing high-performance Pt-based catalysts with low Pt loading is crucial but challenging for CO oxidation. Here, the authors report a novel Pt/TiO2 catalyst consisting of Pt–Ti intermetallic single-atom alloy and Pt nanoparticles to efficiently catalyze CO oxidation.
Designing and enhancing the performance of metal single-atom nanozymes (SAzymes) through atom-pair engineering is important yet difficult. Here the authors develop the atom-pair engineering of Zn-SA/CNCl SAzyme by concurrently creating Zn-N4 sites as catalytic sites and Zn-N4Cl1 sites as catalytic regulators.
Fe-N-C material is promising catalyst for oxygen reduction reaction in proton exchange membrane fuel cell. Here the authors visualize the formation of Fe-N4 sites using in situ heating microscopy, providing theoretical guidance for rational catalyst design of Fe-N-C materials.
Nanosizing covalent organic frameworks using surfactants provides greatly improved water dispersibility and light-harvesting properties, leading to dramatically enhanced photocatalytic hydrogen production performance. Here the authors observe a reverse concentration-dependent photocatalytic phenomeno, whereby a higher photocatalytic activity is found at a lower catalyst concentration.
Hydrogen peroxide photosynthesis is an important reaction that suffers from poor activity due to the high energy barrier of hydrogen extraction in water. Here, we report a keto-form anthraquinone framework that shows promising performance in alkaline conditions.
Polyester waste is increasingly accumulating in the environment, and alcoholysis recycling offers a sustainable management solution. This study demonstrates the use of an oxygen vacancy-rich catalyst to transform waste blended polyester/textiles into high-value monomers.
Designing highly active and stable catalytic sites is often challenging due to complex synthesis procedures and the agglomeration of active sites during high-temperature reactions. Here the authors present a two-step method to synthesize Pt clusters in In-modified ZSM-5, resulting in superior propane dehydrogenation performance.
Photoelectrochemical oxidation of glycerol to produce dihydroxyacetone is limited by its low selectivity. Here, a bismuth vanadate photoanode enriched with a bismuth-rich surface and containing oxygen vacancies was utilized to overcome this dilemma.
Industrial methanol synthesis uses materials based on Cu and ZnO. We present high-resolution imaging of active surfaces which reveals how Zn species are transported at the active Cu interface in diffusion processes controlled by the reactant gas composition.
This study unravels the efficient photocatalytic route for synthesizing dimethoxymethane by coupling CO2 reduction integrated with CH3OH oxidation by using a silver and tungsten comodified blue titanium dioxide catalyst under mild conditions.
Hydrogen spillover is typically associated with reducible metal oxides and considered relevant for various hydrogen-related technologies. Here, the authors demonstrate that a non-reducible MgO doped with heteroatom Al enables hydrogen spillover similarly to reducible metal oxides.
The impact of facets on Fischer-Tropsch synthesis has primarily been explored through theoretical studies or on single-crystal surfaces, lacking experimental data on practical catalysts. Here, the authors provide experimental evidence of the facet sensitivity of iron carbides during syngas conversion by creating {202} and {112} χ-Fe5C2 facets.
Solvents play a crucial role in catalysis, affecting both activity and selectivity. Here the authors demonstrate how solvent affinity to the catalyst surface influences the reaction pathways of 4-propylguaiacol.
Achieving stable and high-activity nitrate electroreduction to ammonia in low concentrations nitrate is critical but challenging. Here, the authors present a Co-based electrocatalyst with gradient-doped Ru atoms, showing a continuous ammonia production at −1000 mA/cm2 in 2000 ppm nitrate electrolyte.
Efficient electroreduction of CO2 to multi-carbon products under strong acidic condition is highly challenging. Here, the authors demonstrate that combining microenvironment modulation and La doping effect could promote multicarbon products generation in acidic electrolyte.
Despite significant progress in CO2 conversion field, there remains a significant gap between fundamental research and the industrial demands. This Comment discusses key performance parameters for industrial applications and outlines current limitations in the field.
Dry reforming of methane (DRM) is a highly endothermic process, often limited by the severe thermocatalytic conditions it demands. Here the authors introduce a novel DRM method that employs a 16 W pulsed laser along with a cost-effective Mo2C catalyst, allowing DRM to proceed under milder conditions.
The catalytic conversion of polyolefins into gasoline-range alkanes requires a comprehensive understanding of the catalytically active species and their corresponding performance. Here the authors tackle this need by examining the nuclearity of the chloroaluminate ions and their interactions with reaction intermediates.
Developing efficient catalysts for syngas-based higher alcohol synthesis (HAS) remains challenging. Here the authors successfully demonstrate an active learning strategy by integrating Bayesian optimization into experimental workflows to accelerate the design of highly active and stable FeCoCuZr catalysts for HAS.
Palladium-based catalysts are highly effective for the complete oxidation of methane. Here, the authors employ operando transmission electron microscopy, near-ambient pressure X-ray photoelectron spectroscopy, and density functional theory calculations to investigate the active state and catalytic function of Pd nanoparticles in methane oxidation.
Tungsten trioxide (WO3) is considered the most promising photocatalyst for the highly selective oxidation of methane to formaldehyde, though the origins of its catalytic activity and reaction mechanism are still debated. Here, the authors use WO3 with {001} and {110} facets as model photocatalysts, demonstrating that the photocatalytic oxidation of methane to formaldehyde in WO3 depends on the surface structure, leading to different formaldehyde selectivity.
The knowledge of semiconductor photocatalysis in C − H bond activation remains limited. Here, the authors report comprehensive mechanistic studies to unveil the semiconductor-rare concerted proton-coupled electron transfer mechanism for C − H bond activation over Zn-In-S.
Creating highly active materials that effectively harness solar spectra is essential for photocatalysis, though challenging. Here the authors introduce a novel donor-acceptor covalent organic framework with a broad absorption range of 200 nm to 900 nm, achieving efficient artificial photocatalytic amine coupling.
Copper nanoclusters have so far been limited in the types of organic transformations they can catalyze. Here the authors introduce a new NIR-II emissive anionic copper nanocluster with intrinsic photoredox activity, enabling efficient photocatalytic three-component radical couplings.
The catalytic partial oxidation of methane (POM) is a promising technology for synthesizing syngas but suffers from severe over-oxidation on the catalyst surface. Here the authors demonstrate that regulating O* occupation in an atomically dispersed MoNi alloy can achieve high catalytic performance for POM.
Crystal facets are known to be important in traditional heterogeneous catalysis, yet this effect has not been studied in plasmon-assisted catalysis. Here, the authors investigate the impact facets have on CO2 reduction using plasmonic Au NPs.
Dry reforming of methane is an attractive route to convert greenhouse gases into valuable syngas. Here, the authors demonstrate design strategy to prepare efficient catalysts towards activation of both C–H and C = O bonds and provide atomic-level insights into interfacial synergistic catalysis.
The exploration of heterogeneous interfaces between metal oxides has received limited attention. Here the authors demonstrated the creation of MnO2-MnxCo3-xO4 interfaces through controlled chemical reduction processes, effectively altering electron distribution and yielding a superior catalyst for ethane oxidation.
The relationship between the structural configurations of M-N-C electrocatalysts and their performances in neutral environments has been insufficiently investigated. Here the authors demonstrate that an ultralow metal-loaded Co-N-C electrocatalyst, featuring the asymmetric Co-C/N/O configuration, exhibit exceptional efficiency in electrochemically producing hydrogen peroxide under neutral conditions.
A robust and efficient dye-sensitized NiO bio-hybrid photocathode based on a redox polymer and [FeFe]- hydrogenase has been developed to couple with a BiVO4 photoanode for water splitting without applied bias.
Proton exchange membrane electrolyzers hold promise for ethylamine synthesis from acetonitrile, yet local acidity fosters proton reduction. Here, authors systematically screen metal catalysts, verifying their effectiveness in such electrolyzers.
An inverse CeAlOx/Ni/Ni-foam structured catalyst with high thermal stability and water resistance is shown to be effective at CO2 methanation across a wide temperature range because of efficient heat/mass transport.
The principle of Le Chatelier is a fundamental concept in textbooks, serving as a guiding principle for controlling chemical and catalytic systems. In this study, the authors present an oxygen electroreduction system based on a single zinc vacancy catalyst, which operates in a manner that extends “beyond” Le Chatelier’s principle.
Physicochemical heterogeneity poses a significant constraint in photocatalyst advancement. Here the authors introduce a multimodal optical microscopy platform to assess activity and defects concurrently in photoelectrocatalysts, revealing that disorder can unexpectedly enhance local photoelectrocatalytic performance in certain instances.
Achieving supported nanoclusters with unique geometric and electronic structures continues to pose a challenge. Here, the authors introduce a plasma-assisted treatment approach for generating supported metal oxide nanoclusters, facilitated by the rapid transformation of monomeric dispersed metal oxides.
Catalyst activation commonly occurs during reactions. This study demonstrates that the surface’s active structure in nitride catalysts during the reverse water gas-shift reaction varies with the partial pressure of reaction products, resulting in enhanced catalytic activity through positive feedback between catalytic activity and the evolution of MoNx’s active structure.
Manganese complexes have long been utilized by nature to catalyze the oxygen evolution reaction (OER) but mirroring their efficiency in artificial electrochemical systems has proven difficult. This study centers on alpha-manganese dioxide (α-MnO2), which closely mimics natural MnIV-O-MnIII-HxO motifs, presenting a novel method for manipulating proton coupling within the OER process using an external electric field.
The transformation of CO2 with renewable hydrogen into high-value products presents a sustainable route for net-zero chemical manufacture. Here the authors introduce a LaFeO3 perovskite-mediated tandem conversion of CO2, achieving remarkable performance by separating the CO2 hydrogenation and C-C coupling domains in the catalyst system.
The ideal metal selection and atomic-level arrangement for catalysts in CO2 hydrogenation are still uncertain. Here, copper is identified as the most effective promoter for enhancing ZnZrOx catalysts when precisely structured into CuZn ensembles, offering new insights for designing superior catalysts for CO2-based methanol synthesis.