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The non-Markovia dynamics of quantum evolution plays an important role in open quantum sytem. However, how to quantify non-Markovian behavior and what can be obtained from non- Markovianity are still open questions, especially in complex solid systems. Here we address the problem of quantifying non-Markovianity with entanglement in a genuine noisy solid state system at room temperature. We observed the non-Markovianity of quantum evolution with entanglement. By prolonging entanglement with dynamical decoupling, we can reveal the non-Markovianity usually concealed in the environment and obtain detailed environment information. This method is expected to be useful in quantum metrology and quantum information science.

Quantum adiabatic evolutions find a broad range of applications in quantum physics and quantum technologies. The traditional form of the quantum adiabatic theorem limits the speed of adiabatic evolution by the minimum energy gaps of the system Hamiltonian. Here, we experimentally show using a nitrogen-vacancy center in diamond that, even in the presence of vanishing energy gaps, quantum adiabatic evolution is possible. This verifies a recently derived necessary and sufficient quantum adiabatic theorem and offers paths to overcome the conventionally assumed constraints on adiabatic methods. By fast modulation of dynamic phases, we demonstrate near-unit-fidelity quantum adiabatic processes in finite times. These results challenge traditional views and provide deeper understanding on quantum adiabatic processes, as well as promising strategies for the control of quantum systems., Comment: With new results

Scalable quantum technologies will require an unprecedented combination of precision and complexity for designing stable structures of well-controllable quantum systems. It is a challenging task to find a suitable elementary building block, of which a quantum network can be comprised in a scalable way. Here we present the working principle of such a basic unit, engineered using molecular chemistry, whose control and readout are executed using a nitrogen vacancy (NV) center in diamond. The basic unit we investigate is a synthetic polyproline with electron spins localized on attached molecular sidegroups separated by a few nanometers. We demonstrate the readout and coherent manipulation of very few ($\leq 6 $) of these $S=1/2$ electronic spin systems and access their direct dipolar coupling tensor. Our results show, that it is feasible to use spin-labeled peptides as a resource for a molecular-qubit based network, while at the same time providing simple optical readout of single quantum states through NV-magnetometry. This work lays the foundation for building arbitrary quantum networks using well-established chemistry methods, which has many applications ranging from mapping distances in single molecules to quantum information processing., Comment: Author name typo

The adiabatic quantum computation is a universal and robust method of quantum computing. In this architecture, the problem can be solved by adiabatically evolving the quantum processor from the ground state of a simple initial Hamiltonian to that of a final one, which encodes the solution of the problem. By far, there is no experimental realization of adiabatic quantum computation on a single solid spin system under ambient conditions, which has been proved to be a compatible candidate for scalable quantum computation. In this letter, we report on the first experimental realization of an adiabatic quantum algorithm on a single solid spin system under ambient conditions. All elements of adiabatic quantum computation, including initial state preparation, adiabatic evolution, and final state readout, are realized experimentally. As an example, we factored 35 into its prime factors 5 and 7 on our adiabatic quantum processor.

Quantum control of systems plays important roles in modern science and technology. The ultimate goal of quantum control is to achieve high fidelity universal control in the time-optimal way. Although high fidelity universal control has been reported in various quantum systems, experimental implementation of time-optimal universal control remains elusive. Here we report the experimental realization of time-optimal universal control of spin qubits in diamond. By generalizing a recent method for solving quantum brachistochrone equations [X. Wang, et al., Phys. Rev. Lett. 114, 170501 (2015)], we obtained accurate minimum time protocols for multiple qubits with fixed qubits' interactions and constrained control field. Single- and two-qubit time-optimal gates are experimentally implemented with fidelities of 99% obtained via quantum process tomography. Our work provides a time-optimal route to achieve accurate quantum control, and unlocks new capabilities for emerging field of time-optimal control in general quantum systems.

Quantum computation provides great speedup over its classical counterpart for certain problems. One of the key challenges for quantum computation is to realize precise control of the quantum system in the presence of noise. Control of the spin-qubits in solids with the accuracy required by fault-tolerant quantum computation under ambient conditions remains elusive. Here, we quantitatively characterize the source of noise during quantum gate operation and demonstrate strategies to suppress the effect of these. A universal set of logic gates in a nitrogen-vacancy centre in diamond are reported with an average single-qubit gate fidelity of 0.999952 and two-qubit gate fidelity of 0.992. These high control fidelities have been achieved at room temperature in naturally abundant 13C diamond via composite pulses and an optimized control method.

We experimentally resolve several weakly coupled nuclear spins in diamond using a series of novelly designed dynamical decoupling controls. Some nuclear spin signals, hidden by decoherence under ordinary dynamical decoupling controls, are shifted forward in time domain to the coherence time range and thus rescued from the fate of being submerged by the noisy spin bath. In this way, more and remoter single nuclear spins are resolved. Additionally, the field of detection can be continuously tuned on sub-nanoscale. This method extends the capacity of nanoscale magnetometry and may be applicable in other systems for high-resolution noise spectroscopy., Comment: 5 pages, 4 figures