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Amorphous nano-metal catalysts often exhibit appealing catalytic properties, because the intrinsic linear scaling relationship can be broken. However, accurate control synthesis of amorphous nano-metal catalysts with desired size and morphology is a challenge. In this work, we discover that Cu(0) could be oxidized to amorphous CuxO species by supercritical CO2. The formation process of the amorphous CuxO is elucidated with the aid of machine learning. Based on this finding, a method to prepare Cu nanoparticles with an amorphous shell is proposed by supercritical CO2 treatment followed by electroreduction. The unique feature of this method is that the size of the particles with amorphous shell can be easily controlled because their size depends on that of the original crystal Cu nanoparticles. Moreover, the thickness of the amorphous shell can be easily controlled by CO2 pressure and/or treatment time. The obtained amorphous Cu shell exhibits high selectivity for C2+ products with the Faradaic efficiency of 84% and current density of 320 mA cm−2. Especially, the FE of C2+ oxygenates can reach up to 65.3 %, which is different obviously from the crystalline Cu catalysts. Amorphous metal catalysts often exhibit appealing catalytic properties, however, accurate control synthesis of amorphous nano-metal catalysts is a challenge. Here, the authors report a feasible strategy to prepare the amorphous Cu catalysts by supercritical CO2 treatment followed by electroreduction. The resulted catalyst shows high selectivity towards multi-carbon products for CO2 electroreduction. [ABSTRACT FROM AUTHOR]

Considerable attention has been drawn to tune the geometric and electronic structure of interfacial catalysts via modulating strong metal-support interactions (SMSI). Herein, we report the construction of a series of TiO2−x/Ni catalysts, where disordered TiO2−x overlayers immobilized onto the surface of Ni nanoparticles (~20 nm) are successfully engineered with SMSI effect. The optimal TiO2−x/Ni catalyst shows a CO conversion of ~19.8% in Fischer–Tropsch synthesis (FTS) process under atmospheric pressure at 220 °C. More importantly, ~64.6% of the product is C2+ paraffins, which is in sharp contrast to the result of the conventional Ni catalyst with the main product being methane. A combination study of advanced electron microscopy, multiple in-situ spectroscopic characterizations, and density functional theory calculations indicates the presence of Niδ−/TiO2−x interfacial sites, which could bind carbon atom strongly, inhibit methane formation and facilitate the C-C chain propagation, lead to the production of C2+ hydrocarbon on Ni surface. Considerable attention has been drawn to tune the geometric and electronic structure of interfacial catalysts via modulating strong metal-support interactions (SMSI). Here the authors report the remarkable catalytic performance of CO hydrogenation over an interfacial TiO2−x/Ni catalyst by means of SMSI. [ABSTRACT FROM AUTHOR]

Electrochemical alcohols oxidation offers a promising approach to produce valuable chemicals and facilitate coupled H2 production. However, the corresponding current density is very low at moderate cell potential that substantially limits the overall productivity. Here we report the electrooxidation of benzyl alcohol coupled with H2 production at high current density (540 mA cm−2 at 1.5 V vs. RHE) over a cooperative catalyst of Au nanoparticles supported on cobalt oxyhydroxide nanosheets (Au/CoOOH). The absolute current can further reach 4.8 A at 2.0 V in a more realistic two-electrode membrane-free flow electrolyzer. Experimental combined with theoretical results indicate that the benzyl alcohol can be enriched at Au/CoOOH interface and oxidized by the electrophilic oxygen species (OH*) generated on CoOOH, leading to higher activity than pure Au. Based on the finding that the catalyst can be reversibly oxidized/reduced at anodic potential/open circuit, we design an intermittent potential (IP) strategy for long-term alcohol electrooxidation that achieves high current density (>250 mA cm−2) over 24 h with promoted productivity and decreased energy consumption. Electrochemical alcohol oxidation offers a promising approach to produce valuable chemicals that can be paired with fuel-producing reactions. Here, authors utilize gold and cobalt oxyhydroxide nanomaterials to obtain industrially-relevant electrolyzer current densities for benzyl alcohol oxidation. [ABSTRACT FROM AUTHOR]

Selective oxidation of ammonia to nitric oxide over platinum-group metal alloy gauzes is the crucial step for nitric acid production, a century-old yet greenhouse gas and capital intensive process. Therefore, developing alternative ammonia oxidation technologies with low environmental impacts and reduced catalyst cost are of significant importance. Herein, we propose and demonstrate a chemical looping ammonia oxidation catalyst and process to replace the costly noble metal catalysts and to reduce greenhouse gas emission. The proposed process exhibit near complete NH3 conversion and exceptional NO selectivity with negligible N2O production, using nonprecious V2O5 redox catalyst at 650 oC. Operando spectroscopy techniques and density functional theory calculations point towards a modified, temporally separated Mars-van Krevelen mechanism featuring a reversible V5+/V4+ redox cycle. The V = O sites are suggested to be the catalytically active center leading to the formation of the oxidation products. Meanwhile, both V = O and doubly coordinated oxygen participate in the hydrogen transfer process. The outstanding performance originates from the low activation energies for the successive hydrogen abstraction, facile NO formation as well as the easy regeneration of V = O species. Our results highlight a transformational process in extending the chemical looping strategy to producing base chemicals in a sustainable and cost-effective manner. This study reports a fundamentally new and commercially promising chemical looping ammonia oxidation scheme using an inexpensive transition metal oxide, and provides mechanistic insight into the oxygen species governing ammonia oxidation. [ABSTRACT FROM AUTHOR]

Atomically dispersed Pt species are advocated as a promising electrocatalyst for the oxygen reduction reaction (ORR) to boost noble metal utilization efficiency. However, when assembled on various substrates, isolated Pt single atoms are often demonstrated to proceed through the two‐electron ORR pathway due to the unfavorable O─O bond cleavage thermodynamics in the absence of catalytic ensemble sites. In addition, although their distinct local coordination environments at the exact single active sites are intensively explored, the interactions and synergy between closely neighboring single atom sites remain elusive. Herein, atomically dispersed Pt monomers strongly interacting on a Mo2C support is demonstrated as a model catalyst in the four‐electron ORR, and the beneficial interactions between two closely neighboring and yet non‐contiguous Pt single atom sites (named as quasi‐paired Pt single atoms) are shown. Compared to isolated Pt single atom sites, the quasi‐paired Pt single atoms deliver a superior mass activity of 0.224 A mg−1Pt and near‐100% selectivity toward four‐electron ORR due to the synergistic interaction from the two quasi‐paired Pt atom sites in modulating the binding mode of reaction intermediates. Our first‐principles calculations reveal a unique mechanism of such quasi‐paired configuration for promoting four‐electron ORR. [ABSTRACT FROM AUTHOR]

Natural enzymes exhibit unparalleled selectivity due to the microenvironment around the active sites, but how to design artificial catalysts to achieve similar performance is a formidable challenge for the catalysis community. Herein, we report that a less selective platinum catalyst becomes highly active and selective for industrially relevant hydrosilylation of a broad range of substrates when a porous cage ligand is used for confinement around the catalytic active site. The catalyst is more than ten times more active than Karstedt's catalyst while being recyclable. Properties such as size-selective catalysis and Michaelis-Menten kinetics support the proposed enzyme-like model. This biomimetic catalyst exhibits remarkable site-selectivity through the cage's confining effect, which amplifies small steric differences into dramatic reactivity changes for similar functional groups within a molecule. Design of artificial catalysts to mimic enzyme activity and selectivity is a challenge in the catalysis field. Here, the authors design a platinum catalyst with a porous cage ligand which shows enzyme-like properties, such as high hydrosilylation activity and substrate size selectivity, while being recyclable. [ABSTRACT FROM AUTHOR]

The industrial synthesis of ammonia (NH3) using iron-based Haber-Bosch catalyst requires harsh reaction conditions. Developing advanced catalysts that perform well at mild conditions (<400 °C, <2 MPa) for industrial application is a long-term goal. Here we report a Co-N-C catalyst with high NH3 synthesis rate that simultaneously exhibits dynamic and steady-state active sites. Our studies demonstrate that the atomically dispersed cobalt weakly coordinated with pyridine N reacts with surface H2 to produce NH3 via a chemical looping pathway. Pyrrolic N serves as an anchor to stabilize the single cobalt atom in the form of Co1-N3.5 that facilitates N2 adsorption and step-by-step hydrogenation of N2 to *HNNH, *NH-NH3 and *NH2-NH4. Finally, NH3 is facilely generated via the breaking of the *NH2-NH4 bond. With the co-existence of dynamic and steady-state single atom active sites, the Co-N-C catalyst circumvents the bottleneck of N2 dissociation, making the synthesis of NH3 at mild conditions possible. The industrial synthesis of ammonia using iron-based Haber-Bosch catalyst requires harsh reaction conditions. Here the authors show co-existence of dynamic and steady-state single atom active sites over Co-N-C catalyst to facilitate nitrogen activation for ammonia synthesis under mild conditions. [ABSTRACT FROM AUTHOR]

Developing effective catalysts based on earth abundant elements is critical for CO2 electroreduction. However, simultaneously achieving a high Faradaic efficiency (FE) and high current density of CO (jCO) remains a challenge. Herein, we prepare a Mn single-atom catalyst (SAC) with a Mn-N3 site embedded in graphitic carbon nitride. The prepared catalyst exhibits a 98.8% CO FE with a jCO of 14.0 mA cm−2 at a low overpotential of 0.44 V in aqueous electrolyte, outperforming all reported Mn SACs. Moreover, a higher jCO of 29.7 mA cm−2 is obtained in an ionic liquid electrolyte at 0.62 V overpotential. In situ X-ray absorption spectra and density functional theory calculations demonstrate that the remarkable performance of the catalyst is attributed to the Mn-N3 site, which facilitates the formation of the key intermediate COOH* through a lowered free energy barrier. Developing effective catalysts based on earth abundant elements is critical for electrochemical CO2 reduction. Here, the authors prepare a manganese single atom catalyst with high CO2 reduction performance, which can be attributed to the Mn-N3 site embedded in graphitic carbon nitride. [ABSTRACT FROM AUTHOR]

The grand challenge in the development of atomically dispersed metallic catalysts is their low metal-atom loading density, uncontrollable localization and ambiguous interactions with supports, posing difficulty in maximizing their catalytic performance. Here, we achieve an interface catalyst consisting of atomic cobalt array covalently bound to distorted 1T MoS2 nanosheets (SA Co-D 1T MoS2). The phase of MoS2 transforming from 2H to D-1T, induced by strain from lattice mismatch and formation of Co-S covalent bond between Co and MoS2 during the assembly, is found to be essential to form the highly active single-atom array catalyst. SA Co-D 1T MoS2 achieves Pt-like activity toward HER and high long-term stability. Active-site blocking experiment together with density functional theory (DFT) calculations reveal that the superior catalytic behaviour is associated with an ensemble effect via the synergy of Co adatom and S of the D-1T MoS2 support by tuning hydrogen binding mode at the interface. While single-atom catalysis offers an efficient materials usage, the ambiguous interactions with supports poses a difficulty in understanding catalytic performances. Here, authors show an ensemble effect via synergy of Co adatoms and the S of MoS2 supports to boost hydrogen evolution activities. [ABSTRACT FROM AUTHOR]

A template-engaged multistep synthesis process is developed to fabricate ultrathin carbon nanosheets assembled hierarchical nanoboxes embedded with dense Mo-N 4 active sites, which exhibited excellent activity and superb stability for oxygen reduction reaction. [Display omitted] • Unique hierarchical SA-Mo-C nanoboxes were fabricated via a template-engaged multistep synthesis process. • Comprehensive characterizations including EXAFS reveal Mo-N 4 atomic sites were formed and densely dispersed in the SA-Mo-C nanoboxes. • SA-Mo-C nanoboxes exhibited better ORR performance compared to commercial Pt/C catalysts. Construction of single-atom catalysts (SACs) with maximally exposed active sites remains a challenging task mainly because of the lack of suitable host matrices. In this study, hierarchical N -doped carbon nanoboxes composed of ultrathin nanosheets with dispersed atomic Mo (denoted as hierarchical SA-Mo-C nanoboxes) were fabricated via a template-engaged multistep synthesis process. Comprehensive characterizations, including X-ray absorption fine structure analysis, reveal the formation of Mo-N 4 atomic sites uniformly anchored on the hierarchical carbon nanoboxes. The prepared catalysts offer structural and morphological advantages, including ultrathin nanosheet units, unique hollow structures and abundant active Mo-N 4 species, that result in excellent activity with a half-wave potential of 0.86 V vs. RHE and superb stability for the oxygen reduction reaction in 0.1 M KOH; thus, the catalysts are promising air–cathode catalysts for Zn-air batteries with a high peak power density of 157.6 mW cm−2. [ABSTRACT FROM AUTHOR]

[Display omitted] • M single atom (M = Fe, Co, Ni) anchored on Ru nanoclusters were prepared to form M 1 Ru SAA. • Co 1 Ru SAA shows the highest NH 3 synthesis rate and TOF Ru value. • Compared with Co-Ru nanoparticle alloy, Co 1 Ru SAA exhibits lower work function and up-shift d band center. • SAA structure effectively tune N 2 activation pathway. The desire of green ammonia (NH 3) production requires efficient catalysts that could operate at mild conditions. However, the activity of catalysts is restricted by scaling relation that low activation energy of N 2 is in conjunction with the over-strong affinity of intermediates, which blocks adsorption sites of catalyst and hinders NH 3 production. Single atom alloy (SAA) is an efficient approach to circumvent this relation. In the present work, we offer a feasible strategy of preparing M 1 Ru (M = Fe, Co, Ni) SAA. Our studies show that Co 1 Ru SAA has the highest NH 3 synthesis rate and the largest TOF Ru value among M 1 Ru SAA. Compared with CoRu nanoparticle alloy (NPA), Co 1 Ru SAA has stronger electronic interaction between Co and Ru, which induces lower work function and up-shift d band center toward Fermi level for Co 1 Ru SAA, thus promoting N 2 activation. Meanwhile, the unique SAA structure could effectively tune N 2 activation pathway. Those findings make a contribution to the development of advanced catalysts for efficient NH 3 synthesis at mild conditions. [ABSTRACT FROM AUTHOR]

[Display omitted] • Unique pompon-like RuCo catalysts were fabricated. • Atomically dispersed Ru-Co sites facilitated the adsorption/activation of reactants. • Excellent catalytic performance was achieved in the guaiacol hydrodeoxygenation. • Ru-Co synergy, as well as favorable hcp structure, contributed to high catalytic efficiency. Currently, the highly efficient conversion of biomass resources into highly valuable chemicals and biofuels is one of the most prospective approaches to reduce greenhouse gases emission and environmental pollution caused by excess consumption of fossil fuels. Herein, three-dimensional pompon-like well-defined RuCo particles with tunable crystallographic structures and surface atomically dispersed Ru atoms were constructed and intensively investigated as support-free metal catalysts in the hydrodeoxygenation (HDO) of lignin-derived guaiacol. It was demonstrated that the 300 °C-reduced RuCo sample possessed the hexagonal close-packed (hcp) crystallographic structure with surface abundant atomically dispersed Ru atoms, whereas 600 °C-reduced RuCo sample presented the face-centered cubic phase with lower surface Ru concentration. The as-fabricated RuCo-300 sample showed excellent catalytic HDO activity with a high cyclohexane yield of 85.3%. Comprehensive structural characterizations unveiled that the introduction of atomically dispersed Ru atoms into the RuCo-300 favored the formation of abundant surface Ru-Co sites, as well as electron-rich Ru0, and such-constructed Ru-Co sites were highly beneficial to the hydrogen dissociation on single Ru0 atoms and the further hydrogen spillover to adjacent Co0 atoms to promote the HDO process. Moreover, density functional theory (DFT) calculations revealed that the hcp structure of RuCo catalysts benefited the adsorption of guaiacol. The unique pompon-like microstructure of RuCo catalysts was conducive to the exposure of active sites and provided more open channels for the easy diffusion of reactants and products. Over the RuCo-300 catalyst, the guaiacol HDO could proceed rapidly via an initial demethoxylation reaction. The present Ru-Co synergetic catalysis in the structure of RuCo catalysts would provide a new strategy for constructing robust heterogeneous bimetal catalysts applied in practical HDO processes of a variety of lignin-derived phenolic compounds. [ABSTRACT FROM AUTHOR]

Urea is of great importance for the survival and development of mankind because of its advantages in effectively increasing crop yields. A novel carbon-supported indium-doped bismuth nanoparticles (Bi: 10 %In/C NPs) was prepared for the synthesis of urea via the co-activated reduction of nitrate and CO 2 with an average Faraday efficiency (FE) of 20.31 % and urea yield (R urea) of 606.38 μg mg−1 h−1. Interestingly, the In doped here not only serves as the active site, but also acts as an activator to stimulate the activity of Bi through electronic interaction, thus making Bi also the active site for the electrocatalytic C-N coupling reaction. Simultaneously, the key intermediates of the reaction are revealed to be *NH 2 and *CO. This work provides further insight into the role of indium in the electrocatalytic C-N coupling for the synthesis of urea, which gives a direction for thinking about the design and construction of subsequent highly efficient electrocatalysts. A novel catalyst based on carbon-supported In-doped Bi nanoparticles (Bi:10 % In/C NPs) was prepared for the co-activated reduction of nitrate and CO 2 for the synthesis of urea with average FE and urea yield of 20.31 % and 606.38 μg mg−1 h−1 at − 0.45 V vs. RHE. The key intermediates of the reaction are revealed to be *NH 2 and *CO. Interestingly, experimental results show that the doped In acts not only as the active site but also as an "activator", stimulating the activity of Bi through electronic interactions, thus making Bi also the active site for electrocatalytic C-N coupling reactions. [Display omitted] ● A bismuth-based catalyst well suited for the electrochemical synthesis of urea (FE: 20.31 %, R urea : 606.38 μg mg−1 h−1) was prepared by a simple room temperature reduction method based on the property of bismuth to inhibit competitive hydrogen evolution reactions. ● A strategy for the preparation of electrocatalysts for highly efficient urea synthesis using direct activation of bismuth by indium is proposed for the first time. ● Theindium in the prepared Bi:In/C not only directly participates in the synthesis of urea as the active site, but also acts as an activator to activate the inert bismuth, so that bismuth also becomes the active site of the C-N coupling reaction, thus greatly improving the efficiency and stability for the synthesis of urea. [ABSTRACT FROM AUTHOR]

• ε-MnO 2 with abundant structure defects was applied in CO oxidation. • Acid washing highly improved catalytic activity of ε-MnO 2. • Enriched surface hydroxyl is the intrinsic reason for the catalytic improvement. • Bicarbonate intermediate desorbs CO 2 faster than carbonate intermediate. Herein, we synthesize the hydroxyl-enriched ε-MnO 2 catalyst (MnO 2 -AT) by simple acid washing. Acid washing destroys the sphere structure into fragments with abundant structure defects and maintains the crystal and pore structure of ε-MnO 2. MnO 2 -AT exhibits the high activity and selectivity for preferential oxidation of CO in the H 2 -rich stream, as well as the high activity for CO total oxidation. It can completely converts CO in preferential and total oxidation of CO at 170 °C and 90 °C, respectively, with a good stability. The acid washing treatment highly increases the surface hydroxyl groups on MnO 2 -AT. Our results demonstrate that with the aid of surface hydroxyl groups CO can easily form bicarbonate intermediates, which are more thermally unstable than carbonate intermediates. The faster CO 2 desorption from bicarbonates than carbonates promotes the CO oxidation process. [ABSTRACT FROM AUTHOR]

• A dynamic N- and H-involved cyclic reaction pathway proposed for NH 3 production. • A dual-path mechanism including chemical looping and thermal catalysis illustrated. • Bottleneck of direct N N dissociation bypassed. The synthesis of ammonia via the Haber-Bosch process using Fe-derived catalysts requires harsh reaction conditions. It is hence meaningful to develop catalysts for low-temperature synthesis of ammonia for industrial application. Herein for the first time, we report that with the synergy between LaN and Ru/ZrH 2 , NH 3 can be synthesized via a dual-path mechanism. The LaN-promoted Ru/ZrH 2 catalyst shows exceptionally high NH 3 synthesis rate (up to 305 mmol NH3 g Ru −1 h−1) at 350 °C under 1 MPa and remarkable durability (tested for 200 h). The outcomes of isothermal surface reaction and a suite of 15N 2 and D 2 isotopic labeling experiments reveal that the N3− of LaN reacts with H− ions to produce NH 3 , leaving behind N and H vacancies. The initial state of Ru/xLaN/ZrH 2 can be restored by having the N and H entities replenished under the atmosphere adopted for NH 3 synthesis. Moreover, based on the results of N 2 reaction order, nitrogen K-edge NEXAFS, in situ XPS as well as in situ DRIFTS analyses under a 25%N 2 -75%D 2 atmosphere, it is reckoned that the direct dissociation of N 2 does not occur on the LaN-promoted Ru/ZrH 2 catalyst while N 2 hydrogenation takes place via an associative pathway under mild conditions. For the hydrogenation of N 2 , an appropriate amount of LaN would induce a synergic effect on the Ru active sites, leading to facile activation and hydrogenation of N 2 to *N 2 H 2. Nonetheless, an excess amount of LaN would result in blocking of Ru sites, consequently hindering the formation of *N 2 H 2 and decreasing the catalytic activity. Following the associative and chemical looping pathways, the LaN-promoted Ru/ZrH 2 catalyst bypasses the bottleneck of N 2 direct dissociation, making the synthesis of NH 3 at mild conditions possible. [ABSTRACT FROM AUTHOR]

• Hierarchically meso-macroporous nanostructured monolithic catalysts are constructed. • Addition of cobalt to CeO 2 nanosheets enhances the redox ability of catalysts. • Co 3 O 4 /CeO 2 monolithic catalysts exhibit high catalytic activity and stability. • Co-Ce interaction generates active surface adsorbed oxygen for soot combustion. Herein, we facilely synthesized the Co 3 O 4 /CeO 2 nanosheets on monolithic Ni foam (Co/Ce-NS) via the tandem hydrothermal and impregnation methods. The constructed hierarchically meso-macroporous nano-structures increase the soot-catalysts contact chances, and promote mass transfer of gaseous reactants and products in catalytic soot combustion. The deposition of Co 3 O 4 nanoparticles onto CeO 2 nanosheets enhances the redox properties of the catalysts, because the Co-Ce interaction generates active surface adsorbed oxygen species for soot combustion. Our results reveal that the adsorbed oxygen species on the Co-Ce interfaces are more active than these on surface CeO 2 or Co 3 O 4. The 0.6Co/Ce-NS catalyst with the optimal cobalt loading has more superficial Co2+-□-Ce3+ couples than other catalysts, consequently generating more active surface adsorbed oxygen species for catalytic soot oxidation. The 0.6Co/Ce-NS catalyst exhibits comparable catalytic activity with the 1%Pt/Al 2 O 3 catalyst under the loose contact condition. Moreover, the 0.6Co/Ce-NS catalyst has the excellent thermal stability and water resistance. Therefore, the hierarchically meso-macroporous Co 3 O 4 /CeO 2 nanosheet monolithic catalysts have potential industrial application in catalytic soot elimination and other related heterogeneous catalytic systems. [ABSTRACT FROM AUTHOR]

• Pt/MnOx and Pt/MnO electrocatalysts were prepared for the oxygen reduction reaction. • Pt-based electrocatalysts showed high utilization efficiency of Pt. • Both Pt-based catalysts exhibited good ORR stability. Electrocatalyst for oxygen-reduction reaction (ORR) is crucial for metal-air batteries, in which Pt-based materials are the benchmark catalysts for ORR. However, the high cost and limited supplies of Pt limit its broad use in commercial applications. Designing highly efficient Pt electrocatalysts can reduce material cost and enable commercial success for a wide variety of electrochemical technologies. Herein, we prepared Pt/MnO x and Pt/MnO electrocatalysts via deposition–precipitation and H 2 –reduction approaches. The Pt mass activities towards the ORR at 0.7 V for the Pt/MnO x , and Pt/MnO catalysts were 4.0 and 3.7 A mg Pt −1, respectively, which were 20, and 18.5 times as commercial 20% Pt/C catalyst. The transferred electron numbers (n) were 3.6 and 4.0 for Pt/MnO x and Pt/MnO, respectively. Moreover, Pt/MnO catalyst exhibited a good ORR stability after 500 cycles compared to Pt/MnO x catalyst in 0.1 M KOH. [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • Dual-bed SCR-LNT system promotes the total lean NOx removal efficiency. • Dual-bed SCR-LNT system is preferable for high-concentration NOx reduction. • Noble metal-free catalyst Cu/Al 2 O 3 and La 0.7 Sr 0.3 CoO 3 are employed. • Dual-bed SCR-LNT system shows a N 2 O selectivity of ∼4%. Abstract A dual-bed fixed-bed reactor consisting of a selective catalytic reduction (SCR) catalyst and a lean NOx trap (LNT) catalyst is designed and employed for high-concentration NOx removal under lean-burn condition. The lean NOx could be partially reduced over the upstream SCR catalyst (Cu/Al 2 O 3) by C 3 H 6 in the stream, greatly increasing the efficiencies of both NOx storage and NOx reduction over the downstream LNT catalyst (La 0.7 Sr 0.3 CoO 3). The activity tests for individual catalyst show that the Cu/Al 2 O 3 containing 5 wt.% Cu is the optimal SCR catalyst, which exhibits similar temperature window of activity (300–350 °C) as the LNT catalyst La 0.7 Sr 0.3 CoO 3. The relative ratio of CuO nanoparticles to surface CuAl 2 O 4 spinel on Cu/Al 2 O 3 is rather important for NO-SCR due to the requirements of appropriate oxidation ability of SCR catalysts. As compared with the single SCR or LNT catalyst, the dual-bed SCR-LNT coupled system shows much lower NOx leak in both lean- and rich-burn periods, especially under the condition of high NOx concentration and high space velocity. Additionally, the NOx to N 2 O selectivity over this coupled system is as low as ∼4%, showing obvious advantage over conventional noble metals-based SCR and LNT catalysts. [ABSTRACT FROM AUTHOR]

[Display omitted] • Ru clusters are immobilized on hierachical Ni 3 N arrays. • The interfacial Ru atoms enable long-range Ni atoms as active sites via electron delocalization. • The H 2 O and H* adsorption energies are strengthened and weakened, respectively. • An outperforming Pt/C benchmark activity is achieved at ≥ 125 mA cm−2. Hydrogen (H 2) production from alkaline water electrocatalysis is economically appealing yet significantly hindered by the sluggish H 2 O adsorption and H* binding kinetics on active sites during hydrogen evolution reaction (HER). Herein, we interfacially immobilize Ru clusters on the hierarchical nickel nitride (Ru-Ni 3 N) nanosheet arrays via the filling of Ru3+ species into the metal vacancies of nickel hydroxide precursors and the subsequent controllable nitridation. The optimized Ru-Ni 3 N shows the outstanding HER performance, affording a 30-fold rise in the intrinsic activity of Ni sites, a outperforming-Pt/C overpotential at ≥ 125 mA cm−2 while remaining a robust stability. We further establish by a combined study of density functional theory (DFT) calculations with experimental analyses that long-range Ni sites around Ru sites act as active sites via the electron delocalization, remarkably weakening the H 2 O adsorption and H* binding barriers for enhancing the alkaline HER kinetics. Moreover, it also demonstrates an excellent pH-universal HER and overall water splitting performance. [ABSTRACT FROM AUTHOR]

Three different pentacoordinate iron phthalocyanine (FePc) electrocatalysts with an axial ligand (pyridyl group, Py) anchored to multi-walled carbon nanotubes (MWCNTs) are prepared by a microwave method as high performance composite electrocatalysts (FePc–Py/MWCNTs) for the oxygen reduction reaction (ORR). For comparison, tetracoordinate FePc electrocatalysts without an axial ligand anchored to MWCNTs (FePc/MWCNTs) are assembled in the same way. Ultraviolet–visible spectrophotometry (UV–Vis), Raman spectroscopy (RS), and high-resolution transmission electron microscopy (HRTEM) are used to characterize the obtained electrocatalysts. The electrocatalytic activity of the samples is measured by linear sweep voltammetry (LSV), and the onset potential of all of the FePc–Py/MWCNTs electrocatalysts is found to be more positive than that of their FePc/MWCNTs counterparts. X-ray photoelectron spectroscopy (XPS) and X-ray absorption fine structure (XAFS) spectroscopy are employed to elucidate the relationship between molecular structure and electrocatalytic activity. XPS indicates that higher concentrations of Fe 3+ and pyridine-type nitrogen play critical roles in determining the electrocatalytic ORR activity of the samples. XAFS spectroscopy reveals that the FePc–Py/MWCNTs electrocatalysts have a coordination geometry around Fe that is closer to the square pyramidal structure, a higher concentration of Fe 3+ , and a smaller phthalocyanine ring radius compared with those of FePc/MWCNTs. [ABSTRACT FROM AUTHOR]

In this study, phosphate FeCo(H 3 O)(PO 4) 2 nanosheet arrays (NAs) were synthesized using an electrochemical strategy. FeCo(H 3 O)(PO 4) 2 NAs as precatalyst could undergo significant self-reconstruction, including leaching of phosphate anions and electro-oxidation of Co2+ during anodizing at the potential range of oxygen evolution reaction (OER) in 1 M KOH solution, eventually resulting in the formation of Fe 0.5 Co 0.5 OOH NAs with low crystallinity. The high content of Fe in Fe 0.5 Co 0.5 OOH NAs promoted the formation of active Fe3+–O–Fe3+ motifs that increased OER occurrence. Additionally, Fe incorporation increased the ratio of the reaction rate constants of oxygen evolution to Co3+/Co4+ (k OER /k M,ox) and enhanced the reaction order on the hydroxyl ion. These factors significantly contributed to the outstanding OER catalytic performances of Fe 0.5 Co 0.5 OOH NAs. [Display omitted] Fe 0.5 Co 0.5 OOH nanosheet arrays (NAs) were fabricated via electrochemical self-reconstruction of CoFe(H 3 O)(PO 4) 2 NAs. Benefiting from the formation of active Fe3+–O–Fe3+ motifs, Fe incorporation increased the ratio of the reaction rate constants of oxygen evolution to Co3+/Co4+ (k OER /k M,ox) and enhanced the reaction order on the hydroxyl ion, Fe 0.5 Co 0.5 OOH NAs exhibited outstanding catalytic performances of oxygen evolution reaction. • Fe 0.5 Co 0.5 OOH was synthesized via self-reconstruction of CoFe(H 3 O)(PO 4) 2. • High content of Fe promoted the formation of [di-μ-O(OH)] Fe3+–O–Fe3+ in Fe 0.5 Co 0.5 OOH. • [di-μ-O(OH)] Fe3+–O–Fe3+ motifs in oxyhdroxide acted as OER active sites. • Fe incorporation varied the electrokinetic parameters of oxyhydroxide. • [di-μ-O(OH)] Fe3+–O–Fe3+ motifs further increased the reaction order on the OH-. [ABSTRACT FROM AUTHOR]

Highlights: [•] CeO2–TiO2 nanorods and nanoparticles are synthesized by different methods. [•] CeO2–TiO2 nanorods are dominated by (110) and (100) facets, while nanoparticles by (111) planes. [•] The catalytic activity of Au/CeO2–TiO2 is strongly related to the morphology of CeO2–TiO2. [•] CeO2–TiO2 nanorods as support endue Au/CeO2–TiO2 with higher activity in CO oxidation. [•] Au dispersion, O2 migration, and redox ability are enhanced in Au/CeO2–TiO2 nanorods. [ABSTRACT FROM AUTHOR]

Highlights: [•] CuO/Co3O4–CeO2 [Ce/(Co+Ce)=1/10] is more efficient for CO PROX than CuO/CeO2. [•] Full CO conversion and 100% selectivity of O2 to CO2 are achieved on it at 98°C. [•] A very wide temperature-window (98–173°C) for full CO conversion is observed. [•] CO is mainly activated and oxidized on Cu+ site by forming carbonyl intermediates. [•] Formation of Cu0 can enhance H2 oxidation, decreasing the O2 to CO2 selectivity. [ABSTRACT FROM AUTHOR]