Dual-Atomic-Site Catalysts for Molecular Oxygen Activation in Heterogeneous Thermo-/Electro-catalysis.

Efficient molecular oxygen activation (MOA) is the key to environmentally friendly catalytic oxidation reactions. In the last decade, single-atomic-site catalysts (SASCs) with nearly 100 % atomic utilization and unique electronic structure have been widely investigated for MOA. However, the single active site makes the activation effect unsatisfactory and difficult to deal with complex catalytic reactions. Recently, dual-atomic-site catalysts (DASCs) have provided a new idea for the effective activation of molecular oxygen (O2 ) due to more diverse active sites and synergetic interactions among adjacent atoms. In this review, we systematically summarized the recent research progress of DASCs for MOA in heterogeneous thermo- and electrocatalysis. Finally, we look forward to the challenges and application prospects in the construction of DASCs for MOA.

Atomic-Layered Cu5 Nanoclusters on FeS2 with Dual Catalytic Sites for Efficient and Selective H2 O2 Activation.

Regulating the distribution of reactive oxygen species generated from H2 O2 activation is the prerequisite to ensuring the efficient and safe use of H2 O2 in the chemistry and life science fields. Herein, we demonstrate that constructing a dual Cu-Fe site through the self-assembly of single-atomic-layered Cu5 nanoclusters onto a FeS2 surface achieves selective H2 O2 activation with high efficiency. Unlike its unitary Cu or Fe counterpart, the dual Cu-Fe sites residing at the perimeter zone of the Cu5 /FeS2 interface facilitate H2 O2 adsorption and barrierless decomposition into ⋅OH via forming a bridging Cu-O-O-Fe complex. The robust in situ formation of ⋅OH governed by this atomic-layered catalyst enables the effective oxidation of several refractory toxic pollutants across a broad pH range, including alachlor, sulfadimidine, p-nitrobenzoic acid, p-chlorophenol, p-chloronitrobenzene. This work highlights the concept of building a dual catalytic site in manipulating selective H2 O2 activation on the surface molecular level towards efficient environmental control and beyond.

Single Mn atom modulated molecular oxygen activation over TiO2 for photocatalytic formaldehyde oxidation.

In single-atom catalysts, the atomically dispersed metal sites are pivotal for oxygen molecule activation. We hypothesize that dispersing single Mn atoms on TiO2 nanosheets may improve the photocatalytic oxidation of formaldehyde (HCHO) in the gas phase under ambient conditions. Density function theory (DFT) and experimental experiments were carried out to single Mn atoms not only improved the transfer of localized electrons and photogenerated electrons but also enhanced the activation/dissociation of O2 to generate monoatomic oxygen ions (O-) as the final reactive oxygen species (ROS). In photocatalytic experiments, Mn/TiO2 photocatalyst removed 100 % of HCHO at a low concentration of 7.6 ppm, and reaching excellent mineralization efficiency of over 99.6 %. According to the proposed reaction mechanism, O2 spontaneously adsorbs onto the Mn/TiO2 surface, forming two adsorbed O- after electron donation into the π2p* antibonding orbitals of O2. The adsorbed O- then reacts with gaseous HCHO to produce the key intermediate dioxymethylene (DOM), finally fulfilling a more favorable oxidation process on the Mn/TiO2 surface. This research illustrates the key role of O- in HCHO oxidation and paves the way for practical HCHO removal using TiO2-based photocatalysts.

Surface oxygen vacancy-dependent molecular oxygen activation for propane combustion over α-MnO2.

Oxygen vacancies (OV), as the sites of molecular oxygen adsorption and activation, play an important role in the catalytic combustion process of volatile organic compounds (VOCs). Revealing the relationship between OV concentration and molecular oxygen activation behavior is of significance to construct the efficient catalysts. Herein, α-MnO2 with different OV concentrations was prepared to investigate the molecular oxygen activation for C3H8 combustion. It is disclosed that the enhanced OV concentration in α-MnO2 induced the reconfiguration of surface metal atoms, resulting in the transformation of oxygen activation configuration from end-on mode to side-on mode. Oxygen molecules in side-on mode possessed more localized electron density and weaker coordination bond strength with surrounding Mn atoms, which were more favorable to adsorb C3H8 molecules and activate C-H bond for the improved combustion performance. This work provides a new understanding to reveal that the increased OV concentration contributes to more efficient VOCs combustion.

A controllable reduction-oxidation coupling process for chloronitrobenzenes remediation: From lab to field trial.

Chloronitrobenzenes (CNBs) are typical refractory aromatic pollutants. The reduction products of CNBs often possess higher toxicity, and the electron-withdrawing substituent groups are detrimental to the ring-opening during the oxidation treatment, leading to ineffective removal of CNBs by either reduction or oxidation technology. Herein we demonstrate a controllable reduction-oxidation coupling (ROC) process composed of zero-valent iron (ZVI) and H2O2 for the effective removal of CNBs from both water and soil. In water, ZVI first reduced p-CNB into 4-chloronitrosobenzene and 4-chloroaniline intermediates, which were then suffered from the subsequent oxidative ring-opening by ·OH generated from the reaction between Fe(II) and H2O2. By controlling the addition time of H2O2, the final mineralization rate of p-CNB reached 6.6 × 10-1 h-1, about 74 times that of oxidation alone (9.0 × 10-3 h-1). More importantly, this controllable ROC process was also applicable for the site remediation of CNBs contaminated soil by either ex-situ treatment or in-situ injection, and, respectively decreased the concentrations of p-CNB, m-CNB, and o-CNB from 1105, 980, and 94 mg/kg to 3, 1, and < 1mg/kg, meeting the remediation goals (p-CNB: < 32.35 mg/kg, o-CNB and m-CNB: < 1.98 mg/kg). These laboratory and field trial results reveal that this controllable ROC strategy is very promising for the treatment of electron-withdrawing groups substituted aromatic contaminates.

Adjacent single-atom irons boosting molecular oxygen activation on MnO2.

Efficient molecular oxygen activation is crucial for catalytic oxidation reaction, but highly depends on the construction of active sites. In this study, we demonstrate that dual adjacent Fe atoms anchored on MnO2 can assemble into a diatomic site, also called as MnO2-hosted Fe dimer, which activates molecular oxygen to form an active intermediate species Fe(O = O)Fe for highly efficient CO oxidation. These adjacent single-atom Fe sites exhibit a stronger O2 activation performance than the conventional surface oxygen vacancy activation sites. This work sheds light on molecular oxygen activation mechanisms of transition metal oxides and provides an efficient pathway to activate molecular oxygen by constructing new active sites through single atom technology.