CO Oxidation Promoted by NO Adsorption on RhMn2O3- Cluster Anions.

CO oxidation represents an important model reaction in the gas phase to provide a clear structure-reactivity relationship in related heterogeneous catalysis. Herein, in combination with mass spectrometry experiments and quantum-chemical calculations, we identified that the RhMn2O3- cluster cannot oxidize CO into gas-phase CO2 at room temperature, while the NO preadsorbed products RhMn2O3-[(NO)1,2] are highly reactive in CO oxidation. This discovery is helpful to get a fundamental understanding on the reaction behavior in real-world three-way catalytic conditions where different kinds of reactants coexist. Theoretical calculations were performed to rationalize the crucial roles of preadsorbed NO where the strongly attached NO on the Rh atom can greatly stabilize the products RhMn2O2-[(NO)1,2] during CO oxidation and at the same time works together with the Rh atom to store electrons that stay originally in the attached CO2- unit. The leading result is that the desorption of CO2, which is the rate-determining step of CO oxidation by RhMn2O3-, can be greatly facilitated on the reactions of RhMn2O3-[(NO)1,2] with CO.

Facile CO bond cleavage on polynuclear vanadium nitride clusters V4N5.

Identifying the structural configurations of precursors for CO dissociation is fundamentally interesting and industrially important in the fields of, e.g., Fischer-Tropsch synthesis. Herein, we demonstrated that CO could be dissociated on polynuclear vanadium nitride V4N5- clusters at room temperature, and a key intermediate, with CO in a N-assisted tilted bridge coordination where the C-O bond ruptures easily, was discovered. The reaction was characterized by mass spectrometry, photoelectron spectroscopy, and quantum-chemistry calculations, and the nature of the adsorbed CO on product V4N5CO- was further characterized by a collision-induced dissociation experiment. Theoretical analysis evidences that CO dissociation is predominantly governed by the low-coordinated V and N atoms on the (V3N4)VN- cluster and the V3N4 moiety resembles a support. This finding strongly suggests that a novel mode for facile CO dissociation was identified in a gas-phase cluster study.

Water-Gas Shift Catalyzed by Iridium-Vanadium Oxide Clusters IrVO2- with Iridium in a Rare Oxidation State of -II.

The discovery of compounds containing transition metals with an unusual and well-established oxidation state is vital to enrich our horizon on formal oxidation state. Herein, benefiting from the study of the water-gas shift reaction (CO + H2O → CO2 + H2) mediated with the iridium-vanadium oxide cluster IrVO2-, the missing -II oxidation state of iridium was identified. The reactions were performed by using our newly developed double ion trap reactors that can spatially separate the addition of reactants and are characterized by mass spectrometry and quantum-chemical calculations. This finding makes an important step that all the proposed 13 oxidation states of iridium (+IX to -III) have been known. The iridium atom in the IrVO2- cluster features the Ir═V double bond and resembles chemically the coordinated oxygen atom. A reactivity study demonstrated that the flexible role switch of iridium between an oxygen-atom like (Ir-IIVO2-) and a transition-metal-atom like behavior (Ir+IIVO3-) in different species can drive the water-gas shift reaction in the gas phase under ambient conditions. This result parallels and well rationalizes the extraordinary reactivity of oxide-supported iridium single-atom catalysts in related condensed-phase reactions.

Catalytic CO Oxidation by O2 Mediated with Single Gold Atom Doped Titanium Oxide Cluster Anions AuTi2 O4-6.

Gas-phase studies on catalytic CO oxidation by O2 mediated with gold-containing heteronuclear metal oxide clusters are vital to obtain the structure-reactivity relationship of supported gold catalysts, while it is challenging to trigger the reactivity of clusters with closed-shell electronic structure in O2 activation. Herein, we identified that CO oxidation by O2 can be catalyzed by the AuTi2 O4-6- clusters, among which AuTi2 O4- with closed-shell electronic structure can effectively activate O2 . The reactions were characterized by mass spectrometry and quantum chemical calculations. Theoretical calculations showed that in the initial stage of O2 activation, the Ti2 O4 moiety in AuTi2 O4- contributes dominantly to activate O2 into superoxide (O2- ⋅) without participation of the Au atom. In subsequent steps, the intimate charge transfer interaction between Au and the Ti2 O4 moiety drives the direct dissociation of the O2- ⋅ unit.

Noble-Metal-Free Single-Atom Catalysts CuAl4 O7-9 - for CO Oxidation by O2.

The single copper atom doped clusters CuAl4 O7-9 - can catalyze CO oxidation by O2 . The CuAl4 O7-9 - clusters are the first group of experimentally identified noble-metal free single atom catalysts for such a prototypical reaction. The reactions were characterized by mass spectrometry and density functional theory calculations. The CuAl4 O9 CO- is much more reactive than CuAl4 O9 - in the reaction with CO to generate CO2 . One adsorbed CO is crucial to stabilize Cu of CuAl4 O9 - around +I oxidation state and promote the oxidation of another CO. The widely emphasized correlation between the catalytic reactivity of CO oxidation and Cu oxidation state can be understood at the strictly molecular level. The remarkable difference between Cu catalysis and noble-metal catalysis was discussed.

Oxidation of SO2 to SO3 by Cerium Oxide Cluster Cations Ce2O4(+) and Ce3O6(.).

Cerium oxide cationic clusters (CeO2)1-3(+) were generated through laser ablation and then reacted with sulfur dioxide (SO2) at ambient conditions in an ion trap reactor and those reactions were studied and characterized by combining the art of time-of-flight mass spectrometry (TOF-MS) with density functional theory (DFT) calculations. Molecule association and oxygen atom transfer (OAT) were observed for the CeO2(+) and (CeO2)2,3(+) reaction systems, respectively. The mechanistic analysis indicates that the weak Ce-O bond strength associated with the oxygen release capacity of cerium oxide clusters is considered as the key factor to achieve the oxidation of SO2. To our best knowledge, this research should be the first example to identify the OAT reactivity of metal oxide cluster ions toward sulfur dioxide under thermal collision conditions, and a fundamental understanding of the elementary oxidation of SO2 to SO3 is provided.

Thermal conversion of methane to formaldehyde promoted by gold in AuNbO3(+) cluster cations.

In addition to generation of a methyl radical, formation of a formaldehyde molecule was observed in the thermal reaction of methane with AuNbO3(+) heteronuclear oxide cluster cations. The clusters were prepared by laser ablation and mass-selected to react with CH4 in an ion-trap reactor under thermal collision conditions. The reaction was studied by mass spectrometry and DFT calculations. The latter indicated that the gold atom promotes formaldehyde formation through transformation of an Au-O bond into an Au-Nb bond during the reaction.

CO Oxidation Promoted by the Gold Dimer in Au2 VO3 (-) and Au2 VO4 (-) Clusters.

Investigations on the reactivity of atomic clusters have led to the identification of the elementary steps involved in catalytic CO oxidation, a prototypical reaction in heterogeneous catalysis. The atomic oxygen species O(.-) and O(2-) bonded to early-transition-metal oxide clusters have been shown to oxidize CO. This study reports that when an Au2 dimer is incorporated within the cluster, the molecular oxygen species O2 (2-) bonded to vanadium can be activated to oxidize CO under thermal collision conditions. The gold dimer was doped into Au2 VO4 (-) cluster ions which then reacted with CO in an ion-trap reactor to produce Au2 VO3 (-) and then Au2 VO2 (-) . The dynamic nature of gold in terms of electron storage and release promotes CO oxidation and O-O bond reduction. The oxidation of CO by atomic clusters in this study parallels similar behavior reported for the oxidation of CO by supported gold catalysts.

Reactivity of oxygen radical anions bound to scandia nanoparticles in the gas phase: C-H bond activation.

The activation of C-H bonds in alkanes is currently a hot research topic in chemistry. The atomic oxygen radical anion (O(-·)) is an important species in C-H activation. The mechanistic details of C-H activation by O(-·) radicals can be well understood by studying the reactions between O(-·) containing transition metal oxide clusters and alkanes. Here the reactivity of scandium oxide cluster anions toward n-butane was studied by using a high-resolution time-of-flight mass spectrometer coupled with a fast flow reactor. Hydrogen atom abstraction (HAA) from n-butane by (Sc2O3)(N)O(-) (N=1-18) clusters was observed. The reactivity of (Sc2O3)(N)O(-) (N=1-18) clusters is significantly sizedependent and the highest reactivity was observed for N=4 (Sc8O13(-)) and 12 (Sc24O37(-)). Larger (Sc2O3)(N)O(-) clusters generally have higher reactivity than the smaller ones. Density functional theory calculations were performed to interpret the reactivity of (Sc2O3)(N)O(-) (N=1-5) clusters, which were found to contain the O(-·) radicals as the active sites. The local charge environment around the O(-·) radicals was demonstrated to control the experimentally observed size-dependent reactivity. This work is among the first to report HAA reactivity of cluster anions with dimensions up to nanosize toward alkane molecules. The anionic O(-·) containing scandium oxide clusters are found to be more reactive than the corresponding cationic ones in the C-H bond activation.

Catalytic NO Reduction by Noble-Metal-Free Vanadium-Aluminum Oxide Cluster Anions.

By using state-of-the-art mass spectrometry and guided by the newly discovered single-electron mechanism (SEM; e.g., Ti3+ + 2NO → Ti4+-O•- + N2O), we determined experimentally that the vanadium-aluminum oxide clusters V4-xAlxO10-x- (x = 1-3) can catalyze the reduction of NO by CO and substantiated theoretically that the SEM still prevails in driving the catalysis. This finding marks an important step in cluster science in which a noble metal had been demonstrated to be indispensable in NO activation mediated by heteronuclear metal clusters. The results provide new insights into the SEM in which active V-Al cooperative communication favors the transfer of an unpaired electron from the V atom to NO attached to the Al atom on which the reduction reaction actually takes place. This study provides a clear picture for improving our understanding of related heterogeneous catalysis, and the electron hopping behavior induced by NO adsorption could be a fundamental chemistry for driving NO reduction.

Structures and reactivity of oxygen-rich scandium cluster anions ScO(3-5)-.

Oxygen-rich scandium cluster anions ScO(3-5)(-) are prepared by laser ablation and allowed to react with n-butane in a fast-flow reactor. A time-of-flight mass spectrometer is used to detect the cluster distribution before and after the reactions. The ScO(3)(-) and ScO(4)(-) clusters can react with n-butane to produce ScO(3)H(-), ScO(3)H(2)(-), and ScO(4)H(-), while the more oxygen-rich cluster ScO(5)(-) is inert. The experiment suggests that unreactive cluster isomers of ScO(3)(-) and ScO(4)(-) are also present in the cluster source. Density functional theory and ab initio methods are used to calculate the structures and reaction mechanisms of the clusters. The theoretical results indicate that the unreactive and reactive cluster isomers of ScO(3,4)(-) contain peroxides (O(2)(2-)) and oxygen-centered radicals (O(.-)), respectively. The mechanisms and energetics for conversion of unreactive O(2)(2-) to reactive O(.-) species are also theoretically studied.

An IrVO4+ Cluster Catalytically Oxidizes Four CO Molecules: Importance of Ir-V Multiple Bonding.

The generation and characterization of multiple metal-metal (M-M) bonds between early and late transition metals is vital to correlate the nature of multiple M-M bonds with the related reactivity in catalysis, while the examples with multiple M-M bonds have been rarely reported. Herein, we identified that the quadruple bonding interactions were formed in a gas-phase ion IrV+ with a dramatically short Ir-V bond. Oxidation of four CO molecules by IrVO4+ is a highly exothermic process driven by the generation of stable products IrV+ and CO2, and then IrV+ can be oxidized by N2O to regenerate IrVO4+. This finding overturns the general impression that vanadium oxide clusters are unwilling to oxidize multiple CO molecules because of the strong V-O bond and that at most two oxygen atoms can be supplied from a single V-containing cluster in CO oxidation. This study emphasizes the potential importance of heterobimetallic multiple M-M bonds in related heterogeneous catalysis.

An Eight-Atom Iridium-Aluminum Oxide Cluster IrAlO6+ Catalytically Oxidizes Six CO Molecules.

Fundamental understanding regarding oxygen storage capacity involving how and why an active site can buffer a large number of oxygen atoms in redox processes is vital to the design of advanced oxygen storage materials, while it is challenging because of the complexity of heterogeneous catalysis. Herein, we identified that an eight-atom iridium-aluminum oxide cluster IrAlO6+ can transfer all the oxygen atoms to catalytically oxidize six CO molecules. This finding represents a breakthrough in cluster catalysis where at most three oxygen atoms from a heteronuclear metal oxide cluster can be catalytically involved in CO oxidation. We found that oxygen prefers to be stored on aluminum to form an O3-• radical in the energetically unfavorable IrAlO6+ isomer and generate the low-coordinated iridium that is pivotal to capturing CO and triggering the catalysis. The powerful electron cycling capability of iridium and the cooperative iridium-aluminum interplay are emphasized to drive the oxygen atom-transfer behavior.

C-H bond activation by aluminum oxide cluster anions, an experimental and theoretical study.

Aluminum oxide cluster anions are produced by laser ablation and reacted with n-butane in a fast flow reactor. A reflectron time-of-flight mass spectrometer is used to detect the cluster distribution before and after the reactions. Aluminum oxide clusters Al2O4,6⁻ and Al3O7⁻ can react with n-C4H10 to produce Al2O4,6H⁻ and Al3O7⁻, respectively, while cluster Al3O6⁻ reacts with n-C4H10 to produce both the Al3O6H⁻ and Al3O6H2⁻. The theoretical calculations are performed to study the structures and bonding properties of clusters Al2O4,6⁻ and Al3O6,7⁻ as well as the reaction mechanism of Al2O4⁻ + n-C4H10. The calculated results show that the mononuclear oxygen-centred radicals (O⁻˙) on Al2O4,6⁻ and Al3O7⁻, and oxygen-centred biradical on Al3O6⁻ are the active sites responsible for the observed hydrogen atom abstraction reactivity. Furthermore, mechanism investigation of the O⁻˙ generation in Al3O7⁻ upon O2 molecule adsorption on un-reactive Al3O5⁻ is performed by theoretical calculations.