Coherence of nitrogen-vacancy electronic spin ensembles in diamond

被引:257
作者
Stanwix, P. L. [1 ,2 ]
Pham, L. M. [3 ]
Maze, J. R. [4 ,5 ]
Le Sage, D. [1 ]
Yeung, T. K. [3 ]
Cappellaro, P. [6 ]
Hemmer, P. R. [7 ]
Yacoby, A. [4 ]
Lukin, M. D. [4 ]
Walsworth, R. L. [1 ,4 ]
机构
[1] Harvard Smithsonian Ctr Astrophys, Cambridge, MA 02138 USA
[2] Univ Western Australia, Sch Phys, Crawley, WA 6009, Australia
[3] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[4] Harvard Univ, Dept Phys, Cambridge, MA 02138 USA
[5] Pontificia Univ Catolica Chile, Fac Fis, Santiago 22, Chile
[6] MIT, Dept Nucl Sci & Engn, Cambridge, MA 02139 USA
[7] Texas A&M Univ, Dept Elect & Comp Engn, College Stn, TX 77843 USA
来源
PHYSICAL REVIEW B | 2010年 / 82卷 / 20期
基金
美国国家科学基金会;
关键词
SINGLE SPINS; DYNAMICS; QUBITS; STATE;
D O I
10.1103/PhysRevB.82.201201
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We present an experimental and theoretical study of electronic spin decoherence in ensembles of nitrogen-vacancy (NV) color centers in bulk high-purity diamond at room temperature. Under appropriate conditions, we find ensemble NV spin coherence times (T(2)) comparable to that of single NV with T(2) > 600 mu s for a sample with natural abundance of (13)C and paramagnetic impurity density similar to 10(15) cm(-3). We also observe a sharp decrease in the coherence time with misalignment of the static magnetic field relative to the NV electronic spin axis, consistent with theoretical modeling of NV coupling to a (13)C nuclear-spin bath. The long coherence times and increased signal-to-noise provided by room-temperature NV ensembles will aid many applications of NV centers in precision magnetometry and quantum information.
引用
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页数:4
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