A 2D porous Fe2O3/graphitic-C3N4/graphene ternary nanocomposite with multifunctions of catalytic hydrogenation, chromium(vi) adsorption and detoxification is reported.

Due to the extraordinary catalytic activity in redox reactions, the noble metal, rhodium, has substantial industrial and laboratory applications in the production of value-added chemicals, synthesis of biomedicine, removal of automotive exhaust gas, and so on. The main drawback of rhodium catalysts is its high-cost, so it is of great importance to maximize the atomic efficiency of the precious metal by recognizing the structure–activity relationship of catalytically active sites and clarifying the root cause of the exceptional performance. This Perspective concerns the significant progress on the fundamental understanding of rhodium chemistry at a strictly molecular level by the joint experimental and computational study of the reactivity of isolated Rh-based gas phase clusters that can serve as ideal models for the active sites of condensed-phase catalysts. The substrates cover the important organic and inorganic molecules including CH4, CO, NO, N2, and H2. The electronic origin for the reactivity evolution of bare Rhxq clusters as a function of size is revealed. The doping effect and support effect as well as the synergistic effect among heteroatoms on the reactivity and product selectivity of Rh-containing species are discussed. The ingenious employment of diverse experimental techniques to assist the Rh1- and Rh2-doped clusters in catalyzing the challenging endothermic reactions is also emphasized. It turns out that the chemical behavior of Rh identified from the gas phase cluster study parallels the performance of condensed-phase rhodium catalysts. The mechanistic aspects derived from Rh-based cluster systems may provide new clues for the design of better performing rhodium catalysts including the single Rh atom catalysts.