...
首页> 外文期刊>Surface Science >In situ XPS study of Pd(111) oxidation. Part 1: 2D oxide formation in 10~(-3) mbar O_2
【24h】

In situ XPS study of Pd(111) oxidation. Part 1: 2D oxide formation in 10~(-3) mbar O_2

机译:Pd(111)氧化的原位XPS研究。第1部分:在10〜(-3)mbar O_2中形成二维氧化物

获取原文
获取原文并翻译 | 示例
           

摘要

The oxidation of the Pd(111) surface was studied by in situ XPS during heating and cooling in 3 x 10~(-3) mbar O_2. A number of adsorbed/dissolved oxygen species were identified by in situ XPS, such as the two dimensional surface oxide (Pd_5O_4), the supersaturated Oads layer, dissolved oxygen and the ((67~(1/2)) x (67~(1/2)))R 12.2° surface structure. Exposure of the Pd(111) single crystal to 3 x 10~(-3) mbar O_2 at 425 K led to formation of the 2D oxide phase, which was in equilibrium with a supersaturated O_(ads) layer. The supersaturated O_(ads) layer was characterized by the O 1s core level peak at 530.37 eV. The 2D oxide, Pd_5O_4, was characterized by two O 1s components at 528.92 eV and 529.52 eV and by two oxygen-induced Pd 3d_(5/2) components at 335.5 eV and 336.24 eV. During heating in 3 x 10~(-3) mbar O_2 the supersaturated O_(ads) layer disappeared whereas the fraction of the surface covered with the 2D oxide grew. The surface was completely covered with the 2D oxide between 600 K and 655 K. Depth profiling by photon energy variation confirmed the surface nature of the 2D oxide. The 2D oxide decomposed completely above 717 K. Diffusion of oxygen in the palladium bulk occurred at these temperatures. A substantial oxygen signal assigned to the dissolved species was detected even at 923 K. The dissolved oxygen was characterised by the O 1s core level peak at 528.98 eV. The "bulk" nature of the dissolved oxygen species was verified by depth profiling. During cooling in 3 x 10~(-3) mbar O_2, the oxidised Pd~(2+) species appeared at 788 K whereas the 2D oxide decomposed at 717 K during heating. The surface oxidised states exhibited an inverse hysteresis. The oxidised palladium state observed during cooling was assigned to a new oxide phase, probably the ((67~(1/2)) x (67~(1/2)))R12.2° structure.
机译:在3 x 10〜(-3)mbar O_2中加热和冷却时,通过原位XPS研究了Pd(111)表面的氧化。通过原位XPS识别了许多吸附/溶解氧物种,例如二维表面氧化物(Pd_5O_4),过饱和Oads层,溶解氧和((67〜(1/2))x(67〜( 1/2)))R 12.2°表面结构。 Pd(111)单晶在425 K下暴露于3 x 10〜(-3)mbar O_2导致形成2D氧化物相,该相与过饱和O_(ads)层处于平衡状态。过饱和的O_(ads)层的特征是O 1s核心能级峰值为530.37 eV。 2D氧化物Pd_5O_4的特征是在528.92 eV和529.52 eV处有两个O 1s组分,在335.5 eV和336.24 eV处有两个氧诱导的Pd 3d_(5/2)组分。在3 x 10〜(-3)mbar O_2中加热时,过饱和的O_(ads)层消失了,而被2D氧化物覆盖的表面部分却增加了。表面被600 K和655 K之间的2D氧化物完全覆盖。通过光子能量变化进行的深度分析证实了2D氧化物的表面性质。 2D氧化物在717 K以上完全分解。在这些温度下,钯主体中的氧扩散。甚至在923 K时也检测到分配给溶解物质的大量氧气信号。溶解氧的特征是在528.98 eV处的O 1s核心能级峰值。溶解氧种类的“本体”性质通过深度剖析来验证。在3 x 10〜(-3)mbar O_2中冷却期间,氧化的Pd〜(2+)物种在788 K处出现,而二维氧化物在加热期间在717 K处分解。表面氧化态表现出逆磁滞。在冷却过程中观察到的氧化钯态被分配给一个新的氧化物相,可能是((67〜(1/2))x(67〜(1/2)))R12.2°结构。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号