PHOTODISSOCIATION OF NO2 ADSORBED ON LIF(001)

被引:28
作者
DIXONWARREN, SJ [1 ]
JACKSON, RC [1 ]
POLANYI, JC [1 ]
RIELEY, H [1 ]
SHAPTER, JG [1 ]
WEISS, H [1 ]
机构
[1] UNIV TORONTO, DEPT CHEM, 80 ST GEORGE ST, TORONTO M5S 1A1, ONTARIO, CANADA
关键词
D O I
10.1021/j100205a070
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
The photochemistry of NO2 physisorbed on single-crystal LiF(001) at 100 K has been studied at lambda1 = 248 nm. The adsorbate was examined by polarized FTIR in both the presence and absence of lambda1 radiation. In the absence of UV irradiation the adlayer is composed of dimeric (NO2)2. In the presence of UV, FTIR shows that some N2O3 is formed. Photodissociations (PDIS) giving both NO(g) and molecular NO2(g) were the predominant mechanisms as determined by time-of-flight mass spectrometry (TOF-MS) and resonantly enhanced multiphoton ionization (REMPI). The main objective of this work was the characterization of the photoproduct, NO, internal state distribution by 1 + 1 REMPI. Vibrational levels from v'' = 0 to 9 were probed with rotational resolution using a tunable laser, lambda2. The rotational distributions for each vibrational level could be described by one Boltzmann temperature. The spin-orbit states of NO(g) were equally populated in all vibrational levels. The lambda doublet states, PI(A') and PI(A''), were equally populated. The principal observation was that the vibrational distribution in NO(g) was inverted and bimodal with a peak in v'' = 0 and a second substantial peak in v'' = 3-4, qualitatively resembling but quantitatively different from that for photolysis of NO2(g). Time delays between the two lasers were used to probe the translational energy of the NO(g) photofragment in specified states of internal excitation. The translational energy distributions were invariant over all vibrational levels, except v'' = 0 for which much slower fragments were observed. This complete determination of the energy distribution in the degrees of freedom of the NO(g) from photodissociation of adsorbate has implications for the identity of the photolyzing species and the dynamics of photodissociation. Two mechanisms for photoformation of NO2(g) were found: one at low coverages and one at higher coverages, the former giving peak translational energies approximately 1.2 kcal/mol and the latter 0.4 kcal/mol.
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页码:10983 / 10994
页数:12
相关论文
共 124 条
[1]   A NOMENCLATURE FOR LAMBDA-DOUBLET LEVELS IN ROTATING LINEAR-MOLECULES [J].
ALEXANDER, MH ;
ANDRESEN, P ;
BACIS, R ;
BERSOHN, R ;
COMES, FJ ;
DAGDIGIAN, PJ ;
DIXON, RN ;
FIELD, RW ;
FLYNN, GW ;
GERICKE, KH ;
GRANT, ER ;
HOWARD, BJ ;
HUBER, JR ;
KING, DS ;
KINSEY, JL ;
KLEINERMANNS, K ;
KUCHITSU, K ;
LUNTZ, AC ;
MCCAFFERY, AJ ;
POUILLY, B ;
REISLER, H ;
ROSENWAKS, S ;
ROTHE, EW ;
SHAPIRO, M ;
SIMONS, JP ;
VASUDEV, R ;
WIESENFELD, JR ;
WITTIG, C ;
ZARE, RN .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (04) :1749-1753
[2]  
ANDERSEN P, 1984, J CHEM PHYS, V80, P2548
[3]  
ANDERSSON LO, 1968, J CHEM SOC CHEM COMM, P99
[4]   VIBRATIONAL AND ROTATIONAL ENERGY-DISTRIBUTION OF NO SCATTERED FROM THE PT(111) CRYSTAL-SURFACE - DETECTION BY 2-PHOTON IONIZATION [J].
ASSCHER, M ;
GUTHRIE, WL ;
LIN, TH ;
SOMORJAI, GA .
PHYSICAL REVIEW LETTERS, 1982, 49 (01) :76-79
[5]   ENERGY REDISTRIBUTION AMONG INTERNAL STATES OF NITRIC-OXIDE MOLECULES UPON SCATTERING FROM PT(111) CRYSTAL-SURFACE [J].
ASSCHER, M ;
GUTHRIE, WL ;
LIN, TH ;
SOMORJAI, GA .
JOURNAL OF CHEMICAL PHYSICS, 1983, 78 (11) :6992-7004
[6]  
BACH W, 1974, DISCUSS FARADAY SOC, V58, P237
[7]   THE ELECTRONIC-SPECTRUM OF NOCL - PHOTOFRAGMENT SPECTROSCOPY, VECTOR CORRELATIONS, AND ABINITIO CALCULATIONS [J].
BAI, YY ;
OGAI, A ;
QIAN, CXW ;
IWATA, L ;
SEGAL, GA ;
REISLER, H .
JOURNAL OF CHEMICAL PHYSICS, 1989, 90 (08) :3903-3914
[8]   ABSOLUTE 2-PHOTON ABSORPTION AND 3-PHOTON IONIZATION CROSS-SECTIONS FOR ATOMIC OXYGEN [J].
BAMFORD, DJ ;
JUSINSKI, LE ;
BISCHEL, WK .
PHYSICAL REVIEW A, 1986, 34 (01) :185-198
[9]   SINGLE-FREQUENCY LASER MEASUREMENTS OF 2-PHOTON CROSS-SECTIONS AND DOPPLER-FREE SPECTRA FOR ATOMIC OXYGEN [J].
BAMFORD, DJ ;
DYER, MJ ;
BISCHEL, WK .
PHYSICAL REVIEW A, 1987, 36 (07) :3497-3500
[10]   PHOTOLYSIS OF ASYM-N2O4 (ONONO2) ISOLATED IN AN ARGON MATRIX AT 11 K [J].
BANDOW, H ;
AKIMOTO, H ;
AKIYAMA, S ;
TEZUKA, T .
CHEMICAL PHYSICS LETTERS, 1984, 111 (4-5) :496-500