The oxygen reduction reaction (ORR) is an important electrode reaction for energy storage and conversion devices based on oxygen electrocatalysis. This paper introduces the thermodynamics, reaction kinetics, reaction mechanisms, and reaction pathways of ORR in aqueous alkaline media. Recent advances of the catalysts for ORR were extensively reviewed, including precious metals, nonmetal-doped carbon, carbon–transition metal hybrids, transition metal oxides with spinel and perovskite structures, and so forth. The applications of those ORR catalysts to zinc–air batteries and alkaline fuel cells were briefly introduced. A concluding remark summarizes the current status of the reaction pathways, advanced catalysts, and the future challenges of the research and development of ORR.

The first use of non-centrosymmetric Janus Au-TiO(2) photocatalysts in efficient, plasmon-enhanced visible-light hydrogen generation is demonstrated. The intense localization of plasmonic near-fields close to the Au-TiO(2) interface, coupled with optical transitions involving localized electronic states in amorphous TiO(2) brings about enhanced optical absorption and the generation of electron-hole pairs for photocatalysis.

A composite made from the assembly of graphene oxide (GO) and copper‐centered metal organic framework (MOF) shows good performance as a tri‐functional catalyst in three important electrocatalysis reactions, namely: the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR). One of the challenges in the area of electrocatalysis is to find an effective catalyst that will reduce, as well as generate, oxygen at moderate temperatures. The enhanced electrocatalytic properties and stability in acid of the GO‐MOF composite is due to the unqiue porous scaffold structure, improved charge transport and synergistic interactions between the GO and MOF. In polymer electrolyte membrane fuel cell testing, the GO‐incorporated Cu‐MOF composite delivers a power density that is 76% that of the commercial Pt catalyst.

Nanosized Pt and PtRu colloids were prepared by a microwave-assisted polyol process and transferred to a toluene solution of decanthiol. Vulcan XC-72 was then added to the toluene solution to adsorb the thiolated Pt and PtRu colloids. TEM examinations showed nearly spherical particles and narrow size distributions for both supported and unsupported metals. The carbon-supported Pt and PtRu nanoparticles were activated by thermal treatment to remove the thiol stabilizing shell. All Pt and PtRu catalysts (except Pt 23 Ru 77 ) showed the X-ray diffraction pattern of a face-centered cubic (fcc) crystal structure, whereas the Pt 23 Ru 77 alloy was more typical of the hexagonal close-packed (hcp) structure. The electro-oxidation of liquid methanol on these catalysts was investigated at room temperature by cyclic voltammetry and chronoamperometry. The results showed that the alloy catalyst was catalytically more active than pure platinum. The heat-treated catalyst was also expectedly more active than the non-heat-treated ones, because of the successful removal of the organic shell, which might interfere with reactant adsorption in the methanol oxidation reaction. Pt 52 Ru 48 /C had the best electrocatalytic performance among all carbon-supported Pt and PtRu catalysts.

A higher yield of functionalized carbon nanotubes (CNTs) was obtained by treatment of CNTs in HNO3 or H2SO4-K2Cr2O7. The deposition of platinum nanoparticles and nanoclusters on these functionalized multiwalled carbon nanotubes by electroless plating was facilitated by a two-step sensitization-activation pretreatment. The deposition was sensitive to the aging time of the sensitizing solution and the pH of the plating solution. The resulting electrocatalysts were characterized by transmission electron microscopy, X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry. XPS analysis showed that the Pt/CNT electrocatalysts contained 67.3% of Pt(0) and 32.7% of Pt(IV). Test runs on a single stack polymer electrolyte membrane fuel cell showed that these electrocatalysts are very promising for fuel cell applications.

Highly active and durable air cathodes to catalyze both the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are urgently required for rechargeable metal-air batteries. In this work, an efficient bifunctional oxygen catalyst comprising hollow Co O nanospheres embedded in nitrogen-doped carbon nanowall arrays on flexible carbon cloth (NC-Co O /CC) is reported. The hierarchical structure is facilely derived from a metal-organic framework precursor. A carbon onion coating constrains the Kirkendall effect to promote the conversion of the Co nanoparticles into irregular hollow oxide nanospheres with a fine scale nanograin structure, which enables promising catalytic properties toward both OER and ORR. The integrated NC-Co O /CC can be used as an additive-free air cathode for flexible all-solid-state zinc-air batteries, which present high open circuit potential (1.44 V), high capacity (387.2 mAh g , based on the total mass of Zn and catalysts), excellent cycling stability and mechanical flexibility, significantly outperforming Pt- and Ir-based zinc-air batteries.

In this work, a networked MoS2/CNT nanocomposite has been synthesized by a facile solvothermal method. The as-prepared sample exhibits high catalytic activity for electrocatalytic hydrogen evolution.

Well-defined ultrathin MoS2 nanoplates are developed by a facile solvent-dependent control route from single-source precursor for the first time. The obtained ultrathin nanoplate with a thickness of ~ 5 nm features high density of basal edges and abundant unsaturated active S atoms. The multistage growth process is investigated and the formation mechanism is proposed. Ultrathin MoS2 nanoplates exhibit an excellent activity for hydrogen evolution reaction (HER) with a small onset potential of 0.09 V, a low Tafel slope of 53 mV dec(-1), and remarkable stability. This work successfully demonstrates that the introduction of unsaturated active S atoms into ultrathin MoS2 nanoplates for enhanced electrocatalytic properties is feasible through a facial one-step solvent control method, and that this may open up a potential way for designing more efficient MoS2-based catalysts for HER.