کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5377112 | 1389380 | 2006 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Spin solitons in organic charge-transfer salts
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی تئوریک و عملی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Organic charge-transfer (CT) salts that crystallize in face-to-face stacks of Ï-electron donors (D) and acceptors (A) are one-dimensional electronic systems with strong coupling to lattice and molecular vibrations. Peierls-Hubbard models of CT salts resemble Ï-electron theory of conjugated polymers, although transfer integrals t along mixed DA stacks are considerably smaller. Strong D and A yield Peierls systems with dimerized ground states of ion radicals, D+ and Aâ. Topological spin solitons separate regions of opposite dimerization, similarly to solitons in trans-polyacetylene, but are thermally accessible in ionic CT salts due to small t. Salts with still smaller t have Peierls transitions at TPÂ <Â 300Â K to undimerized stacks. A Peierls-Hubbard model, HCT, describes both types of salts and estimates of t are consistent with TPÂ <Â 300Â K in some salts and spin solitons in others with higher TP. Electron paramagnetic resonance (epr) spectra of single crystals provide direct evidence for spin solitons and one-dimensional electronic states. Spin solitons and HCT resolve longstanding conflicts between vibrational and magnetic data that indicate dimerized stacks in several prototypical CT salts, while structural data point to undimerized stacks with large thermal ellipsoids. The low energy scale, availability of single crystals and diversity of CT salts offer opportunities for detailed modeling.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Physics - Volume 325, Issue 1, 9 June 2006, Pages 60-70
Journal: Chemical Physics - Volume 325, Issue 1, 9 June 2006, Pages 60-70
نویسندگان
Sharon A. Bewick, Zoltán G. Soos,