Boundary of quantum evolution under decoherence

被引:88
作者
Khaneja, N [1 ]
Luy, B
Glaser, SJ
机构
[1] Harvard Univ, Div Appl Sci, Cambridge, MA 02138 USA
[2] Tech Univ Munich, Inst Organ Chem & Biochem, D-85747 Garching, Germany
关键词
D O I
10.1073/pnas.2134111100
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
Relaxation effects impose fundamental limitations on our ability to coherently control quantum mechanical phenomena. In this article, we use principles of optimal control theory to establish physical limits on how closely a quantum mechanical system can be steered to a desired target state in the presence of relaxation. In particular, we explicitly compute the maximum amplitude of coherence or polarization that can be transferred between coupled hetero-nuclear spins in large molecules at high magnetic fields in the presence of relaxation. Very general decoherence mechanisms that include cross-correlated relaxation have been included in our analysis. We give analytical characterization for the pulse sequences (control laws) that achieve these physical limits and provide supporting experimental evidence. Exploitation of cross-correlation effects has recently led to the development of powerful methods in NMR spectroscopy to study very large biomolecules in solution. For two heteronuclear spins, we demonstrate with experiments that cross-correlated relaxation optimized pulse (CROP) sequences provide significant gains over the state-of-the-art methods. It is shown that despite large relaxation rates, coherence can be transferred between coupled spins without any loss in special cases where cross-correlated relaxation rates can be tuned to autocorrelated relaxation rates.
引用
收藏
页码:13162 / 13166
页数:5
相关论文
共 29 条
[1]  
Alicki R., 2007, Volume 717 of Lecture Notes in Physics, V717
[2]  
[Anonymous], 2018, Mathematical Theory of Optimal Processes
[3]  
[Anonymous], 1824, REFLECTIONS PUISSANC
[4]   2-DIMENSIONAL SPECTROSCOPY - APPLICATION TO NUCLEAR MAGNETIC-RESONANCE [J].
AUE, WP ;
BARTHOLDI, E ;
ERNST, RR .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (05) :2229-2246
[5]  
Ayscough P.B., 1967, Electron Spin Resonance in Chemistry
[6]   Stabilization of quantum computations by symmetrization [J].
Barenco, A ;
Berthiaume, A ;
Deutsch, D ;
Ekert, A ;
Jozsa, R ;
Macchiavello, C .
SIAM JOURNAL ON COMPUTING, 1997, 26 (05) :1541-1557
[7]  
BODENHAUSEN G, 1981, PROG NMR SPECTROSC, V14, P137
[8]  
BRUSCHWEILER R, 1992, J CHEM PHYS, V96, P1758, DOI 10.1063/1.462131
[9]  
Bryson A. E., 1975, APPL OPTIMAL CONTROL
[10]   NET POLARIZATION TRANSFER VIA A J-ORDERED STATE FOR SIGNAL ENHANCEMENT OF LOW-SENSITIVITY NUCLEI [J].
BURUM, DP ;
ERNST, RR .
JOURNAL OF MAGNETIC RESONANCE, 1980, 39 (01) :163-168