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Updated: Sep 15, 2025

Dissolution Dynamic Nuclear Polarization Instrumentation for Real-time Enzymatic Reaction Rate Measurements by NMR
Published on: February 23, 2016
Simulation of pulsed dynamic nuclear polarization in the steady state
Shebha Anandhi Jegadeesan1, Yujie Zhao2, Graham M Smith2
1Department of Chemistry, University of Konstanz, Konstanz, Germany.
None:
In pulsed dynamic nuclear polarization (DNP), enhancement of bulk nuclear polarization requires the repeated application of a microwave pulse sequence. So far, analysis of a one-time transfer of electron spin polarization to a dipolar-coupled nuclear spin has guided the design of DNP pulse sequences. This has obvious shortcomings, such as the inability to predict the optimal repetition time. In an actual pulsed DNP experiment, a balance is reached between the polarization arriving from the unpaired electrons and nuclear relaxation. In this article, we explore three algorithms to compute this stroboscopic steady state: (1) explicit time evolution by propagator squaring, (2) generation of an effective propagator using the matrix logarithm, and (3) direct calculation of the steady state with the Newton-Raphson method. Algorithm (2) is numerically unstable in dissipative DNP settings. Algorithms (1) and (3) are both stable; algorithm (3) is the most efficient. We compare the steady-state simulations to existing experimental results at 0.34 and 1.2 T and to the first experimental observation of X-inverse-X (XiX) DNP at 3.4 T. The agreement is good and improves further when electron-proton distance and electron Rabi frequency distributions are accounted for. We demonstrate that the trajectory of the spin system during one-time application of a microwave pulse sequence differs from the steady orbit. This has implications for DNP pulse sequence design.
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