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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.
Kim and co-workers introduce a new ‘kinetic site deconvolution’ method to identify active sites on heterogeneous catalysts by linking reaction rates to specific adsorption environments.
The authors report an in situ investigation of interfacial hydrogen spillover in Pd/ZIF-8 structures with X-ray and Raman techniques. A mechanistic picture of how Pd/ZIF-8 catalyst mediate alkyne semihydrogenation to alkynes is described.
This study demonstrates the effectiveness and generality of utilizing ultrathin Cu-based hydrotalcite-like hydroxy salts as catalysts for infrared light-driven CO2 reduction based on their d-d orbital transition mechanism.
Redispersion of sintered metal species requires high temperatures in reactive atmospheres. Here, the authors report room temperature redispersion of supported Cu particles via formation of mobile hydroxylated Cu species induced by gaseous H2O and anchoring of the Cu species by surface OH groups.
High-pressure infrared spectroscopy shows concentrated cations suppress CO adsorption. Here the authors report two electrochemical interfaces forming distinct double layer structures and reaction rates at elevating pressure and various potentials.
The increasing production of lithium-ion batteries and plastics presents significant challenges to resource sustainability and ecosystem integrity. This study highlights the utilization of spent lithium cobalt oxide cathodes as photothermal catalysts to transform various waste polyesters into valuable monomers.
Principal interest lies in diatomic catalysts (DACs) for efficient CO2 to C2H4 photoconversion yet optimizing catalytic performance and exploring reaction mechanisms are impeded by heteronuclear atom random distribution. Here, a novel up-bottom ion-cutting architecture is proposed for fabricating well-defined DACs.
Dissolution of Co atoms in acidic media impedes the application of cobalt oxides in proton exchange membrane water electrolyzers. Here, the authors reveal a stabilizing effect induced by Ir single atoms on cobalt oxides that suppress Co dissolution.
Here, authors report an inter-site structural heterogeneity induced effect of hierarchical single atom Fe catalysts for robust oxygen reduction. Dynamic evolutions and insights into structure-activity relationship are presented.
Temperature has demonstrated the potential to regulate the photocatalytic oxygen evolution reaction (OER). This study confirms that the temperature-induced bubble-water/catalyst triphase interface microenvironment significantly enhances OER by optimizing the formation and deprotonation of semi-hydrophobic OH radicals.
The semi-hydrogenation of alkynes faces the trade-off between activity and selectivity due to undesirable over-hydrogenation. Here the authors report an efficient additive-free WO3-based single-atom Pd catalytic system with a vertical size effect of hydrogen spillover to mediate the trade-off between activity and selectivity.
Elucidating structure-function relationships is crucial for developing efficient catalysts. Here, the authors elucidate Pt single atom coordination environments on anatase TiO2 and correlate active site structure with CO oxidation activity.
Isolated Rh3+ sites are stabilized inside the MFI zeolite channels with phosphorous which is added during zeolite synthesis in the form of a phosphonium zeolite template. This Rh3+ shows high activity in the low-temperature ethylene hydroformylation.
In this work, the authors design a Mo2N/MoO2-x nonmetallic plasmonic catalyst by regulating synergy between two specific active sites. Highly efficient, selective, and durable CO2 hydrogenation under relatively mild reaction conditions is achieved
Savateev et al. investigate proton-coupled electron transfer from persistent graphitic carbon nitride radical to oxygen and imines. The results of their study find application in cascade photocatalysis – selective tetramerization of benzylic amines.
The selective oxidative dehydrogenation of ethane is attracting increasing attention as a method for ethylene production. Here, PdZn supported on ZnO affords record-breaking photocatalytic ethane-to-ethylene conversion rate, emphasizing the pivotal role of the interface between PdZn and ZnO in the process.
Designing catalysts with atomically synergistic sites shows great promise as a pathway for advanced catalyst development. Here the authors report Zn-Cr catalyst with atomically binuclear active sites for iso-stoichiometric co-conversion of ethane and CO2 through proximal atomic synergy.
Efforts to produce aromatic monomers through catalytic lignin depolymerization were focused on aryl–ether bond cleavage, while the carbon–carbon bonds of a large fraction of aromatic monomers in lignin are difficult to cleave. Here, the authors report a catalytic autoxidation method using manganese and zirconium salts as catalysts to cleave the C–C bonds in lignin-derived dimers and oligomers from pine and poplar.
Zhu et al. report a quantitative and time-resolved analysis of hydrogen activation on Ga2O3, specifically shedding light on the long-standing puzzle of homolytic dissociation as opposed to the heterolytic pathway on oxides.
Yin et al. reveal a protonation pathway in CO2 photoreduction on TiO2, challenging electron activation theories and diversifying photocatalyst design, distinct from Fischer-Tropsch and Sabatier processes.
An air-stable plasmonic catalyst using Pt-Ru on black gold achieves 90% selectivity in acetylene semi-hydrogenation using plasmonic photochemistry. Mechanistic experiments highlight the role of non-thermal and thermal effects for this reaction.
Lithium carbonate-promoted mixed rare earth oxides can be used as redox catalysts for OCM at 700 °C and achieve a single-pass C2+ yield up to 30.6%. The high activity is assigned to the peroxide and OH radicals induced by Pr4+ in the redox catalyst.
Inexpensive iron catalysts often exhibit low activity in ammonia decomposition due to a strong iron-nitrogen binding energy. Here the authors demonstrate that combining iron with cobalt to form a Fe-Co bimetallic catalyst overcomes this limitation, presenting a promising solution for enhancing ammonia decomposition efficiency.
Efficiently producing multicarbon chemicals through electrochemical CO2 reduction is essential for achieving economically feasible carbon neutrality. Here, the authors present molecularly enhanced CO2-to-*CO conversion and *CO dimerization for high-rate ethylene production by nanoconfinement of ascorbic acid.
Understanding the structure-stability relationship of catalysts is imperative for the development of high performance electrocatalytic devices. Here the authors use operando attenuated total reflectance surface-enhanced infrared absorption spectroscopy to quantitatively monitor the evolution of Cu single-atom catalysts in electrochemical CO2 reduction.
Research into the dynamics of chemical reactions at the single-molecule level is a pivotal undertaking. Here, the authors present a direct investigation of the chemiluminescent reaction dynamics of single molecules in solution, providing spatiotemporally resolved insights into chemical reactions.
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.
Deconvoluting and quantitating ligand effect from the typical strain-ligand effects in a real catalytic structure remains challenging. Here, the authors report a core/shell catalyst model to quantitate how much ligand effect solely contributes to electrocatalytic performance through experimental design.
Electrocatalytic nitrate reduction to ammonia has emerged as an alternative strategy for effluent treatment and ammonia production. Here, the authors report a pulsed potential approach to overcome the sluggish reaction kinetics caused by the limited distribution of negatively charged nitrate near the working electrode and the competing side reactions.
Investigation of the reaction process at the single-bond interface is key to understanding the catalytic reaction mechanism. Here, the authors develop a STM-BJ method to monitor the catalytic process from the perspective of single-bond energy.
Chlor-alkali process plays an important role in the chemical industry. However, large overpotential and low selectivity of currently used catalysts lead to high energy consumption. Here the authors report Ru-O4 single site catalysts for chlorination evolution with 1000 h stability at 1000 mA cm−2 in a seawater-like environment.
Tandem concepts for electroreduction of CO2 offer a valuable toolkit to tackle sluggish reaction kinetics and raise the production of e-chemicals. Here, the authors report a cascade system with two coupled electrolyzers using Ni-N-C and Cu-based catalysts for enhanced CO2 to multi-carbon conversion
Achieving stable and selective chlorine production is of high interest yet challenging. Here the authors report an amorphous CoOxCly catalyst prepared by in situ electrodeposition in acidic saline electrolyte which shows ~100% chlorine evolution selectivity with low overpotential and high stability over 500 h.
Electrooxidation of biomass provides a sustainable route to produce valuable chemicals, but suffers from non-Faradaic degradation in alkaline electrolysis at high reactant concentration. Here, the authors develop a single-pass continuous flow reactor to tackle this challenge, achieving kilogram-scale and continuous electrooxidation of glucose to formate and 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid with high selectivity and high concentration.
Chalcogen-bridged naphthalene diimide coordination polymers are designed and synthesised as potent excited state reductants for the activation of inert bonds in a series of aryl halides.
This work develops defective MnO2 catalysts with Frustrated Lewis Pairs through a coordination number reduction strategy to enhance the aerobic oxidation of various polyols/sugars to formic acid.
Deciphering the reaction mechanisms of CO/CO2 electroreduction to methanol remains challenging. Here the authors report the higher electron density of single-Co-atom center, along with a different adsorption configuration of *CO, is crucial for promoting the CO electroreduction to methanol.
The mechanism of how interfacial wettability impacts the CO2 electcgq Herein, the authors describe the design and realization of controllable equilibrium of kinetic controlled *CO and *H to reveal its contribution to ethylene and ethanol pathways.
Direct solar-driven methane (CH4) reforming is highly desirable but challenging. Here, the synergy of atomic Cu species and partially reduced tungsten (Wδ+), stabilized over an oxygen-vacancy-rich WO3, enables exceptional CH4 conversion to formaldehyde (HCHO) under visible light.
The donor-acceptor (D-A) interaction and exciton binding energy have been investigated for a series of D-A pairs by DFT calculations. Here, the authors synthesize the corresponding D-A COFs, and demonstrate that their photocatalytic hydrogen production activities match well with the calculation results.
Efficient ethylene removal below room temperatures is of great importance to food transportation and storage. Here the authors have developed an efficient gold-platinum nanoalloy catalyst for trace ethylene removal at 0 °C for 15 days.
Cu-based catalysts for the conversion of C2H2 to C2H4 are plagued by side reactions. Here, Cu nanodots for C2H2 semihydrogenation are reported to reach current densities >400 mA cm−2 and selectively produce polymer-grade ethylene over 130 h.
Polymer dielectrics face huge challenges in the harsh environments of emergent applications. Now, increased energy storage of polymer dielectrics at temperatures up to 250 °C by designing tailored combinations of structural units is reported.
Potassium oxide is used as a promotor in industrial ammonia synthesis, although metallic potassium is better in theory. Here, the authors demonstrate metallic potassium, an unstable metal that easily volatilizes at high temperature, can be used as a promotor for ammonia synthesis.
Non-oxidative dehydrogenation technologies suffer from the thermodynamic equilibrium limitations and severe coking. Here, the authors report the intensified propane dehydrogenation to propylene by the chemical looping engineering on nanoscale core-shell redox catalysts.