We report the synthesis and characterization of a solid solution series of cationic metal−organic materials with full compositional range from pure Co(II) to Zn(II) endmembers. The materials consist of [Zn x Co 1−x (H 2 O) 4 (4,4′bipy) 2 ] 2+ metal−organic clusters that π−π stack into 2-D positively charged layers, with the metal ratio tunable by molar ratio under hydrothermal conditions. The interlamellar α,ωalkanedisulfonate serves as an anionic template and noncovalently interacts with the cationic layers. The weak interaction allows anion exchange for toxic oxometal anions, such as chromate, CrO 4 2− . The highest chromate adsorption capacity was 68.5 mg/g (0.43 mol/mol) for the as-synthesized 50 mol % Co(II)-incorporated material. Our cationic material can also selectively trap these toxic oxo-anions when nontoxic anions (e.g., nitrate, sulfate) were present in an over 50-fold excess concentration.

We report the results of a systematic study of the catalytic activity of mass-selected vanadium oxide clusters deposited on rutile TiO2 surfaces under ultrahigh vacuum (UHV) conditions. Our results show that supported V, VO, and VO2 clusters are not catalytically active for the oxidative dehydrogenation of methanol to formaldehyde but can be made catalytically active by postoxidation. In addition, we found that the postoxidized VO/TiO2 produces the most formaldehyde. Scanning tunneling microscopy (STM) imaging of the postoxidized VO/TiO2 reveals isolated clusters with height and width indicative of VO3 bound to the TiO2 surface. Our results are consistent with previous density functional theory (DFT) calculations that predict that VO3 will be produced by postoxidation of VO and that VO3/TiO2 is an active catalyst.

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We probe the adsorption of molecular H 2 O on a TiO 2 (110)-(1 × 1) surface decorated with isolated VO clusters using ultrahigh-vacuum scanning tunneling microscopy (UHV-STM) and temperature-programmed desorption (TPD). Our STM images show that preadsorbed VO clusters on the TiO 2 (110)-(1 × 1) surface induce the adsorption of H 2 O molecules at room temperature (RT). The adsorbed H 2 O molecules form strings of beads of H 2 O dimers bound to the 5-fold coordinated Ti atom (5c-Ti) rows and are anchored by VO. This RT adsorption is completely reversible and is unique to the VOdecorated TiO 2 surface. TPD spectra reveal two new desorption states for VO stabilized H 2 O at 395 and 445 K, which is in sharp contrast to the desorption of water due to recombination of hydroxyl groups at 490 K from clean TiO 2 (110)-(1 × 1) surfaces. Density functional theory (DFT) calculations show that the binding energy of molecular H 2 O to the VO clusters on the TiO 2 (110)-(1 × 1) surface is higher than binding to the bare surface by 0.42 eV, and the resulting H 2 O−VO−TiO 2 (110) complex provides the anchor point for adsorption of the string of beads of H 2 O dimers.