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In a typical synthesis, aqueous solutions of K2PtCl4 (Alfa Aesar, 99.9%) and C14TABr (Aldrich, 99%) were mixed in a 20-mL vial at room temperature. The mixture was heated at 50 8C for about 5 min until the solution became clear. The vial was capped with a rubber septum immediately after adding ice-cold NaBH4 (Strem Chemicals, 98%) and the H2 gas pressure inside the vial was released through a needle in the septum for 10 min. The needle was then removed and the solution was kept at 50 8C for 6 h. When l-ascorbic acid (Aldrich, 99 + %) was used as the reducing agent the solution was kept at 70 8C. The total volume of the solution was maintained at 10 mL. When necessary, H2 gas was passed through the solution slowly for 5 min and then pressurized for 1 min without an exit needle. The product was centrifuged at 3000 rpm for 30 min. The supernatant solution was separated and centrifuged again at 12000 rpm for 10 min. The precipitate was collected and re-dispersed in 5 mL of deionized water by sonication. UV/Vis absorption spectra were recorded with an Agilent 8453 UV/Vis system. TEM and HRTEM images were obtained with a Jeol 200CX microscope and a Philips CM200 microscope, respec-tively, operating at 200 kV, at the National Center for Electron Microscopy at the Lawrence Berkeley National Laboratory. The surface area was measured with a Quantachrome Autosorb-1 analyzer at 77 K using nitrogen as the adsorption gas. Before the measurement, degassing was conducted at 150 8C for 48 h to remove possible moisture. The pH value was measured with a Mettler Toledo MP220 pH meter. [ Last edited by ÈÕÔÂÏàÖª on 2012-4-11 at 21:28 ] |
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