Active Thermochemical Tables: The Adiabatic Ionization Energy of Hydrogen Peroxide

被引:35
作者
Changala, P. Bryan [1 ,2 ]
Nguyen, T. Lam [3 ,4 ]
Baraban, Joshua H. [5 ]
Ellison, G. Barney [5 ]
Stanton, John F. [3 ,4 ]
Bross, David H. [6 ]
Ruscic, Branko [6 ,7 ]
机构
[1] NIST, JILA, Boulder, CO 80309 USA
[2] Univ Colorado Boulder, Boulder, CO 80309 USA
[3] Univ Florida, Dept Chem, Quantum Theory Project, Gainesville, FL 32611 USA
[4] Univ Florida, Dept Phys, Quantum Theory Project, Gainesville, FL 32611 USA
[5] Univ Colorado, Dept Chem, Boulder, CO 80302 USA
[6] Argonne Natl Lab, Chem Sci & Engn Div, 9700 S Cass Ave, Argonne, IL 60439 USA
[7] Univ Chicago, Computat Inst, Chicago, IL 60637 USA
基金
美国国家科学基金会;
关键词
MOLECULAR ELECTRONIC-STRUCTURE; COUPLED-CLUSTER THEORY; FULL CCSDT MODEL; CARBON-MONOXIDE; PHOTOELECTRON-SPECTROSCOPY; NITROUS-OXIDE; BASIS-SETS; HEATS; METHANE; IMPLEMENTATION;
D O I
10.1021/acs.jpca.7b06221
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 adiabatic ionization energy of hydrogen peroxide (HOOH) is investigated, both by means of theoretical calculations and theoretically assisted reanalysis of previous experimental data. Values obtained by three different approaches: 10.638 +/- 0.012 eV (purely theoretical determination), 10.649 +/- 0.005 eV (reanalysis of photoelectron spectrum), and 10.645 +/- 0.010 eV (reanalysis of photoionization spectrum) are in excellent mutual agreement. Further refinement of the latter two values to account for asymmetry of the rotational profile of the photoionization origin band leads to a reduction of 0.007 +/- 0.006 eV, which tends to bring them into even closer alignment with the purely theoretical value. Detailed analysis of this fundamental quantity by the Active Thermochemical Tables approach, using the present results and extant literature, gives a final estimate of 10.641 +/- 0.006 eV.
引用
收藏
页码:8799 / 8806
页数:8
相关论文
共 51 条
[1]   GENERAL CONTRACTION OF GAUSSIAN-BASIS SETS .1. ATOMIC NATURAL ORBITALS FOR 1ST-ROW AND 2ND-ROW ATOMS [J].
ALMLOF, J ;
TAYLOR, PR .
JOURNAL OF CHEMICAL PHYSICS, 1987, 86 (07) :4070-4077
[2]  
[Anonymous], 1972, MOL SPECTROSCOPY MOD
[3]   STUDY OF SOME MEDIUM SIZE ALCOHOLS AND HYDROPEROXIDES BY PHOTOELECTRON-SPECTROSCOPY [J].
ASHMORE, FS ;
BURGESS, AR .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1977, 73 :1247-1261
[4]   The heats of combustion of carbon monoxide in oxygen and of nitrous oxide in carbon monoxide at constant pressure [J].
Awbery, JH ;
Gritfiths, E .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-CONTAINING PAPERS OF A MATHEMATICAL AND PHYSICAL CHARACTER, 1933, 141 (843) :1-16
[5]   High-accuracy extrapolated ab initio thermochemistry.: II.: Minor improvements to the protocol and a vital simplification [J].
Bomble, Yannick J. ;
Vazquez, Juana ;
Kallay, Mihaly ;
Michauk, Christine ;
Szalay, Peter G. ;
Csaszar, Attila G. ;
Gauss, Juergen ;
Stanton, John F. .
JOURNAL OF CHEMICAL PHYSICS, 2006, 125 (06)
[6]   Coupled-cluster methods including noniterative corrections for quadruple excitations -: art. no. 054101 [J].
Bomble, YJ ;
Stanton, JF ;
Kállay, M ;
Gauss, J .
JOURNAL OF CHEMICAL PHYSICS, 2005, 123 (05)
[7]   THE VAPOR PRESSURE AND HEAT OF SUBLIMATION OF GRAPHITE [J].
BREWER, L ;
GILLES, PW ;
JENKINS, FA .
JOURNAL OF CHEMICAL PHYSICS, 1948, 16 (08) :797-807
[8]   DETERMINATION OF STANDARD GIBBS ENERGY CHANGE FOR CO + 1/2O2 = CO2 USING AN ELECTROCHEMICAL PUMP AND GAUGE [J].
CANEIRO, A ;
FOULETIER, J ;
KLEITZ, M .
JOURNAL OF CHEMICAL THERMODYNAMICS, 1981, 13 (09) :823-832
[9]   A vacuum ultraviolet laser pulsed field ionization-photoion study of methane (CH4): determination of the appearance energy of methylium from methane with unprecedented precision and the resulting impact on the bond dissociation energies of CH4 and CH4+ [J].
Chang, Yih-Chung ;
Xiong, Bo ;
Bross, David H. ;
Ruscic, Branko ;
Ng, C. Y. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2017, 19 (14) :9592-9605
[10]  
Cox J.D., 1989, CODATA Key Values for Thermodynamics