Mechanisms of Auger-induced chemistry derived from wave packet dynamics

被引:28
作者
Su, Julius T. [1 ]
Goddard, William A., III [1 ]
机构
[1] CALTECH, Mat & Proc Simulat Ctr, Pasadena, CA 91125 USA
关键词
electron force field; fermionic molecular dynamics; floating Gaussian orbitals; PHOTON-STIMULATED DESORPTION; DIAMOND SURFACES; HYDROGEN;
D O I
10.1073/pnas.0812087106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To understand how core ionization and subsequent Auger decay lead to bond breaking in large systems, we simulate the wave packet dynamics of electrons in the hydrogenated diamond nanoparticle C197H112. We find that surface core ionizations cause emission of carbon fragments and protons through a direct Auger mechanism, whereas deeper core ionizations cause hydrides to be emitted from the surface via remote heating, consistent with results from photon-stimulated desorption experiments [ Hoffman A, Laikhtman A, ( 2006) J Phys Condens Mater 18: S1517-S1546]. This demonstrates that it is feasible to study the chemistry of highly excited large-scale systems using simulation and analysis tools comparable in simplicity to those used for classical molecular dynamics.
引用
收藏
页码:1001 / 1005
页数:5
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