By simply adjusting the molar ratio of resorcinol (R) to formaldehyde (F) and optimizing the aging time of the gel, highly ordered mesoporous carbons (OMCs) have been synthesized under strong acidic conditions through aqueous self-assembly of R/F with triblock copolymer F127, without addition of any promoters. It was found that both the excess amount of R (R/F g 1/2) and the long aging time (96 h) were favorable to the formation of the OMC. This facile route was further extended to the synthesis of highly ordered iridium-containing mesoporous carbons (Ir-OMC) by adding H 2 IrCl 6 to the reaction mixture. The resultant Ir-OMCs were characterized by nitrogen sorption, X-ray diffraction (XRD), and transmission electron microscopy (TEM). The results showed that iridium particles, with sizes of ∼2 nm, were highly dispersed in the carbon matrix, while the ordered mesostructure of carbons remained well. Comparing with the Ir/OMC sample prepared by postimpregnation, such one-pot synthesized Ir-OMC samples had smaller Ir particles sizes and therefore exhibited higher activities and stabilities toward the catalytic decomposition of N 2 H 4 .

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The sorption isotherms of CO 2 in wet ordered mesoporous silica KIT-6 with different amounts of pre-adsorbed water were firstly collected experimentally using a volumetric method in the temperature range of 275-281 K. The isotherms show an inflection point indicating CO 2 hydrates form in the pore spaces which is proofed by the enthalpy change calculated at the inflection pressure, and the quantity of water content shows considerable effect on the sorption capacity of CO 2 . The highest enhancement of sorption capacity in the presence of water is observed in wet KIT-6 sample with water loadings of 2.48, which is about 12.80 mmol/g and 1.86 times than that on dry sample. However, the saturation capacity is still far less than that what can be stored merely in the form of hydrates due to the low ratio of water utilization because of the large pore and the polar surface of KIT-6.