Department of Applied Chemistry, Faculty of Science and Engineering, Kinki University, Kowakae, Higashiosaka, Osaka 577-8502, Japan.
J Am Chem Soc. 2012 Sep 5;134(35):14526-33. doi: 10.1021/ja305225s. Epub 2012 Aug 22.
Au/CeO(2) samples with various Au contents were prepared by the multistep (MS) photodeposition method. Their properties including Au particle size, particle dispersion, and photoabsorption were investigated and compared with properties of samples prepared by using the single-step (SS) photodeposition method. The MS- and SS-Au/CeO(2) samples were used for selective oxidation of benzyl alcohols to corresponding benzaldehydes in aqueous suspensions under irradiation by visible light from a green LED, and the correlations between reaction rates and physical properties of the MS- and SS-Au/CeO(2) samples were investigated. Difference in the two photodeposition methods was reflected in the average size and number of Au nanoparticles, for example, 92 nm and 1.3 × 10(12) (g-Au/CeO(2))(-1) for MS photodeposition and 59 nm and 4.8 × 10(12) (g-Au/CeO(2))(-1) for SS photodeposition in the case of 1.0 wt % Au samples. Fixation of larger Au particles resulted in strong photoabsorption of the MS-Au/CeO(2) samples at around 550 nm due to the surface plasmon resonance, and the Kubelka-Munk function of the photoabsorption linearly increased with increase in Au content up to 2.0 wt %, in contrast to the photoabsorption of SS-Au/CeO(2) samples, which was weak and was saturated even at around 0.5 wt %. Due to the strong photoabsorption, the MS-Au/CeO(2) samples exhibited reaction rates approximately twice larger than those of SS-Au/CeO(2) samples with the same Au contents, and apparent quantum efficiency of MS-Au/CeO(2) reached 4.9% at 0.4 mW cm(-2). Linear correlations were observed between reaction rates (r) and surface area of Au nanoparticles (S) in both MS- and SS-Au/CeO(2) samples, though the two slopes of r versus S plots were different, suggesting that oxidation of benzyl alcohol occurred on the Au surface and that S was one of the important factors controlling the reaction rate. Photocatalytic oxidation of benzyl alcohol having an amino group revealed that the Au/CeO(2) photocatalyst exhibited high chemoselectivity toward the hydroxyl group of alcohol, i.e, the Au/CeO(2) photocatalyst almost quantitatively converted aminobenzyl alcohol to aminobenzaldehyde with 99% yield.
采用多步(MS)光沉积法制备了具有不同金含量的 Au/CeO(2) 样品。研究了它们的性质,包括金颗粒尺寸、颗粒分散性和光吸收,并与采用单步(SS)光沉积法制备的样品的性质进行了比较。MS-和 SS-Au/CeO(2) 样品在绿光 LED 可见光照射下,用于在水悬浮液中选择性氧化苄醇生成相应的苯甲醛,研究了 MS-和 SS-Au/CeO(2) 样品的反应速率与物理性质之间的相关性。两种光沉积方法的差异反映在金纳米粒子的平均尺寸和数量上,例如,对于 1.0wt%Au 样品,MS 光沉积为 92nm 和 1.3×10(12)(g-Au/CeO(2))(-1),而 SS 光沉积为 59nm 和 4.8×10(12)(g-Au/CeO(2))(-1)。较大金颗粒的固定导致 MS-Au/CeO(2) 样品在约 550nm 处由于表面等离子体共振而具有强烈的光吸收,并且光吸收的 Kubelka-Munk 函数随 Au 含量的增加线性增加,直至 2.0wt%,而 SS-Au/CeO(2) 样品的光吸收较弱,甚至在约 0.5wt%时就达到饱和。由于强烈的光吸收,MS-Au/CeO(2) 样品的反应速率大约是具有相同 Au 含量的 SS-Au/CeO(2) 样品的两倍,并且 MS-Au/CeO(2) 的表观量子效率在 0.4mW cm(-2)时达到 4.9%。在 MS-和 SS-Au/CeO(2) 样品中,观察到反应速率(r)与 Au 纳米颗粒表面积(S)之间存在线性相关性,尽管 r 与 S 关系图的两个斜率不同,这表明苄醇的氧化发生在 Au 表面上,并且 S 是控制反应速率的重要因素之一。具有氨基的苄醇的光催化氧化表明,Au/CeO(2) 光催化剂对醇的羟基具有高化学选择性,即 Au/CeO(2) 光催化剂几乎定量地将氨基苄醇转化为氨基苯甲醛,产率为 99%。