超原子
X射线光电子能谱
电子亲和性(数据页)
化学
二十面体对称
离子
兴奋剂
分析化学(期刊)
光电发射光谱学
质谱
原子物理学
结晶学
电子结构
材料科学
核磁共振
分子
计算化学
物理
光电子学
色谱法
有机化学
作者
Shun Ito,Yuriko Tasaka,Katsunosuke Nakamura,Yuki Fujiwara,Keisuke Hirata,Kiichirou Koyasu,Tatsuya Tsukuda
标识
DOI:10.1021/acs.jpclett.2c01284
摘要
The electron binding energies of the ligand-protected gold/silver-based cluster anions, [Au25(SR)18]-, [XAg24(SR')18]2- (X = Ag+, Au+, Pd0, or Pt0), and [PdAu24(C≡CR″)18]2- having icosahedral M13 superatomic cores, were reexamined by gas-phase photoelectron spectroscopy (PES) on a significantly intensified mass-selected ion beam. Laser fluence-dependent PE spectra and pump-probe PES revealed that the previous PE spectra were contaminated by PE signals due to the two-photon electron detachment via long-lived photoexcited states. Although the adiabatic electron affinities (AEAs) of the corresponding oxidized forms were found to be 1-2 eV larger than those previously reported, the effects of doping and ligation were not qualitatively affected. (1) The AEA of the Ag13 superatom (∼4 eV) was not appreciably affected by doping a Au atom at the center but was reduced by ∼2 eV by doping Pd or Pt, and (2) the AEA of PdAu12 protected by Au2(C≡CR″)3 units was much larger than that of PdAg12 protected by Ag2(SR')3 units.
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