Wang J, Cotoros I, Dani K M, Liu X, Furdyna J K, Chemla D S
Materials Sciences Division, Lawrence Berkeley National Laboratory and Department of Physics, University of California at Berkeley, Berkeley, California 94720, USA.
Phys Rev Lett. 2007 May 25;98(21):217401. doi: 10.1103/PhysRevLett.98.217401. Epub 2007 May 22.
We report on the observation of ultrafast photoenhanced ferromagnetism in GaMnAs. It is manifested as a transient magnetization increase on a 100 ps time scale, after an initial subpicosecond demagnetization. The dynamic magnetization enhancement exhibits a maximum below the Curie temperature T(c) and dominates the demagnetization component when approaching T(c). We attribute the observed ultrafast collective ordering to the p-d exchange interaction between photoexcited holes and Mn spins, leading to a correlation-induced peak around 20 K and a transient increase in T(c).
我们报道了在砷化镓锰(GaMnAs)中观察到的超快光增强铁磁性。它表现为在初始亚皮秒退磁之后,在100皮秒时间尺度上的瞬态磁化强度增加。动态磁化增强在居里温度T(c)以下呈现最大值,并且在接近T(c)时主导退磁分量。我们将观察到的超快集体有序归因于光激发空穴与锰自旋之间的p-d交换相互作用,这导致了在20 K左右出现一个关联诱导峰以及T(c)的瞬态增加。