Orienting polar molecules without hexapoles: Optical state selection with adiabatic orientation

被引:15
作者
Schaefer, Tim [1 ]
Bartels, Nils [1 ]
Hocke, Nils [1 ]
Yang, Xueming [2 ]
Wodtke, Alec M. [1 ,3 ,4 ]
机构
[1] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
[2] Dalian Inst Chem Phys, Dalian, Peoples R China
[3] Max Planck Inst Biophys Chem, Dept Dynam Surfaces, D-37077 Gottingen, Germany
[4] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会;
关键词
BORN-OPPENHEIMER APPROXIMATION; ASYMMETRIC-TOP MOLECULES; ENERGY-TRANSFER; METAL-SURFACES; DIPOLE-MOMENT; NO; SPECTROSCOPY; EXCITATION; DYNAMICS; STICKING;
D O I
10.1016/j.cplett.2012.03.056
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A pedagogic review of technology used to orient polar molecules is presented to place in context the report of a new approach to this problem. Laboratory frame orientation of polar molecules is achieved by state-specific optical pumping in a region free of electric fields followed by adiabatic transport into a static electric field. This approach overcomes some of the limitations of the more common hexapole focusing method. In particular the method is nearly insensitive to the kinetic energy of the sample. We demonstrate production of oriented samples of NO (mu(el) = 0.15 D) with translational energies above 1 eV in both high-and low-field seeking states. The method can be extended to many other classes of molecules, including near symmetric tops and ions. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:1 / 11
页数:11
相关论文
共 61 条
[1]   Energy transfer at metal surfaces: the need to go beyond the electronic friction picture [J].
Bartels, Christof ;
Cooper, Russell ;
Auerbach, Daniel J. ;
Wodtke, Alec M. .
CHEMICAL SCIENCE, 2011, 2 (09) :1647-1655
[2]   FOKUSSIERUNG POLARER MOLEKULE [J].
BENNEWITZ, HG ;
PAUL, W ;
SCHLIER, C .
ZEITSCHRIFT FUR PHYSIK, 1955, 141 (1-2) :6-15
[3]   MESSUNG DER ANISOTROPIE DES VAN DER WAALS-POTENTIALS DURCH STREUUNG VON MOLEKULEN IN DEFINIERTEM QUANTENZUSTAND [J].
BENNEWITZ, HG ;
KRAMER, KH ;
TOENNIES, JP ;
PAUL, W .
ZEITSCHRIFT FUR PHYSIK, 1964, 177 (01) :84-&
[4]   The role of molecular state and orientation in harpooning reactions:: N2O on Cs/Pt(111) [J].
Brandt, M ;
Greber, T ;
Bowering, N ;
Heinzmann, U .
PHYSICAL REVIEW LETTERS, 1998, 81 (11) :2376-2379
[5]   HEXAPOLE STATE SELECTION AND FOCUSING VS BRUTE FORCE ORIENTATION OF BEAM MOLECULES [J].
BULTHUIS, J ;
VANLEUKEN, JJ ;
STOLTE, S .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1995, 91 (02) :205-214
[6]   Rotational effects in dissociation of H2 on Pd(111):: Quantum and classical study [J].
Busnengo, HF ;
Pijper, E ;
Kroes, GJ ;
Salin, A .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (23) :12553-12562
[7]   Electrostatic Hexapole State-Selection of the Asymmetric-Top Molecule Propylene Oxide [J].
Che, Dock-Chil ;
Palazzetti, Federico ;
Okuno, Yasuhiro ;
Aquilanti, Vincenzo ;
Kasai, Toshio .
JOURNAL OF PHYSICAL CHEMISTRY A, 2010, 114 (09) :3280-3286
[8]   Hexapole transport and focusing of vibrationally excited NO molecules prepared by optical pumping [J].
Chen, J ;
Matsiev, D ;
White, JD ;
Murphy, M ;
Wodtke, AM .
CHEMICAL PHYSICS, 2004, 301 (2-3) :161-172
[9]   LASER STARK SPECTROSCOPY OF FORMALDEHYDE-D2 - CORIOLIS COUPLED V4 AND V6 FUNDAMENTALS [J].
COFFEY, D ;
YAMADA, C ;
HIROTA, E .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1977, 64 (01) :98-108
[10]   Reinvestigation of the emission gamma band system (A(2)Sigma(+)-X(2)Pi) of the NO molecule [J].
Danielak, J ;
Domin, U ;
Kepa, R ;
Rytel, M ;
Zachwieja, M .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1997, 181 (02) :394-402