arXiv subjects

Peter C. Maurer

Publications and source records attributed to Peter C. Maurer.

16 recordsLinked to original sources

arXiv2026

A Surface-Scaffolded Molecular Qubit

Fluorescent spin qubits are central building blocks of quantum technologies. Placing these qubits at surfaces maximizes coupling to nearby spins and fields, enabling nanoscale sensing and facilitating integration with photonic and superconducting devices. However, reducing the dimensions or size of established qubit systems without sacrificing the qubit performance or degrading the coherence lifetime remains challenging. Here, we introduce a surface molecular qubit formed by pentacene molecules scaffolded on a two-dimensional (2D) material, hexagonal boron nitride (hBN). The qubit exhibits stable fluorescence and optically detected magnetic resonance (ODMR) from cryogenic to ambient conditions. With fully deuterated pentacene, the Hahn-echo coherence reaches 22 $μ$s and further extends to 214 $μ$s under dynamical decoupling, outperforming state-of-the-art shallow NV centers in diamond, despite being positioned directly on the surface. We map the local spin environment, resolving couplings to nearby nuclear and electron spins that can serve as auxiliary quantum resources. This platform combines true surface integration, long qubit coherence, and scalable fabrication, opening routes to quantum sensing, quantum simulation, and hybrid quantum devices. It also paves the way for a broader family of 2D material-supported molecular qubits.

quant-ph↗

arXiv2025

Engineering diamond interfaces free of dark spins

Nitrogen-vacancy (NV) centers in diamond are extensively utilized as quantum sensors for imaging fields at the nanoscale. The ultra-high sensitivity of NV magnetometers has enabled the detection and spectroscopy of individual electron spins, with potentially far-reaching applications in condensed matter physics, spintronics, and molecular biology. However, the surfaces of these diamond sensors naturally contain electron spins, which create a background signal that can be hard to differentiate from the signal of the target spins. In this study, we develop a surface modification approach that eliminates the unwanted signal of these so-called dark electron spins. Our surface passivation technique, based on coating diamond surfaces with a thin titanium oxide (TiO$_2$) layer, reduces the dark spin density. The observed reduction in dark spin density aligns with our findings on the electronic structure of the diamond-TiO$_2$ interface. The reduction, from a typical value of $2,000$~$μ$m$^{-2}$ to a value below that set by the detection limit of our NV sensors ($200$~$μ$m$^{-2}$), results in a two-fold increase in Hahn-echo coherence time of near surface NV centers. Furthermore, we derive a comprehensive spin model that connects dark spin relaxation with NV coherence, providing additional insights into the mechanisms behind the observed spin dynamics. Our findings are directly transferable to other quantum platforms, including nanoscale solid state qubits and superconducting qubits.

quant-ph↗

arXiv2025

Quantum biosensing on a multiplexed functionalized diamond microarray

Quantum sensing with nitrogen-vacancy (NV) centers in diamond promises to revolutionize biological research and medical diagnostics. Thanks to their high sensitivity, NV sensors could, in principle, detect specific binding events with metabolites and proteins in a massively parallel and label-free way, avoiding the complexity of mass spectrometry. Realizing this vision has been hindered by the lack of quantum sensor arrays that unite high-density spatial multiplexing with uncompromising biochemical specificity. Here, we introduce a scalable quantum biosensing platform that overcomes these barriers by integrating the first multiplexed DNA microarray directly onto a subnanometer antifouling diamond surface. The 7x7 DNA array, patterned onto a diamond chip, enables simultaneous detection of 49 distinct biomolecular features with high spatial resolution and reproducibility, as verified by fluorescence microscopy. Molecular recognition is converted into a quantum signal via a target-induced displacement mechanism in which hybridization removes a Gd$^{3+}$-tagged DNA strand, restoring NV center spin relaxation times (T$_1$) and producing a binary quantum readout. This platform establishes a new paradigm for high-throughput, multiplexed quantum biosensing and opens the door to advanced molecular diagnostics and large-scale quantum sensor networks operable in complex biological environments.

physics.ins-det↗

arXiv2025

Enhancing Noisy Quantum Sensing by GHZ State Partitioning

Presence of harmful noise is inevitable in entanglement-enhanced sensing systems, requiring careful allocation of resources to optimize sensing performance in practical scenarios. We advocate a simple but effective strategy to improve sensing performance in the presence of noise. Given a fixed number of quantum sensors, we partition the preparation of GHZ states by preparing smaller, independent sub-ensembles of GHZ states instead of a GHZ state across all sensors. We perform extensive analytical studies of the phase estimation performance when using partitioned GHZ states under realistic noise -- including state preparation error, particle loss during parameter encoding, and sensor dephasing during parameter encoding. We derive simple, closed-form expressions that quantify the optimal number of sub-ensembles for partitioned GHZ states. We also examine the explicit noisy quantum sensing dynamics under dephasing and loss, where we demonstrate the advantage from partitioning for maximal QFI, short-time QFI increase, and the sensing performance in the sequential scheme. The results offer quantitative insights into the sensing performance impact of different noise sources and reinforce the importance of resource allocation optimization in realistic quantum applications.

quant-ph↗

arXiv2025

Probing cellular activity via charge-sensitive quantum nanoprobes

Nitrogen-vacancy (NV) based quantum sensors hold great potential for real-time single-cell sensing with far-reaching applications in fundamental biology and medical diagnostics. Although highly sensitive, the mapping of quantum measurements onto cellular physiological states has remained an exceptional challenge. Here we introduce a novel quantum sensing modality capable of detecting changes in cellular activity. Our approach is based on the detection of environment-induced charge depletion within an individual particle that, owing to a previously unaccounted transverse dipole term, induces systematic shifts in the zero-field splitting (ZFS). Importantly, these charge-induced shifts serve as a reliable indicator for lipopolysaccharide (LPS)-mediated inflammatory response in macrophages. Furthermore, we demonstrate that surface modification of our diamond nanoprobes effectively suppresses these environment-induced ZFS shifts, providing an important tool for differentiating electrostatic shifts caused by the environment from other unrelated effects, such as temperature variations. Notably, this surface modification also leads to significant reductions in particle-induced toxicity and inflammation. Our findings shed light on systematic drifts and sensitivity limits of NV spectroscopy in a biological environment with ramification on the critical discussion surrounding single-cell thermogenesis. Notably, this work establishes the foundation for a novel sensing modality capable of probing complex cellular processes through straightforward physical measurements.

physics.app-ph↗

arXiv2025

A fluorescent-protein spin qubit

Optically-addressable spin qubits form the foundation of a new generation of emerging nanoscale sensors. The engineering of these sensors has mainly focused on solid-state systems such as the nitrogen-vacancy (NV) center in diamond. However, NVs are restricted in their ability to interface with biomolecules due to their bulky diamond host. Meanwhile, fluorescent proteins have become the gold standard in bioimaging, as they are genetically encodable and easily integrated with biomolecules. While fluorescent proteins have been suggested to possess a metastable triplet state, they have not been investigated as qubit sensors. Here, we realize an optically-addressable spin qubit in the Enhanced Yellow Fluorescent Protein (EYFP) enabled by a novel spin-readout technique. A near-infrared laser pulse allows for triggered readout of the triplet state with up to 44% spin contrast. Using coherent microwave control of the EYFP spin at liquid-nitrogen temperatures, we measure a spin-lattice relaxation time of $(141 \pm 5)\, \mathrm{μs}$, a $(16 \pm 2)\, \mathrm{μs}$ coherence time under Carr-Purcell-Meiboom-Gill (CPMG) decoupling, and a predicted oscillating (AC) magnetic field sensitivity with an upper bound of $183 \, \mathrm{fT}\, \mathrm{mol}^{1/2}\, \mathrm{Hz}^{-1/2}$. We express the qubit in mammalian cells, maintaining contrast and coherent control despite the complex intracellular environment. Finally, we demonstrate optically-detected magnetic resonance at room temperature in aqueous solution with contrast up to 3%, and measure a static (DC) field sensitivity with an upper bound of $93 \, \mathrm{pT}\, \mathrm{mol}^{1/2}\, \mathrm{Hz}^{-1/2}$. Our results establish fluorescent proteins as a powerful new qubit sensor platform and pave the way for applications in the life sciences that are out of reach for solid-state technologies.

quant-ph↗

arXiv2024

Direct-bonded diamond membranes for heterogeneous quantum and electronic technologies

Diamond has superlative material properties for a broad range of quantum and electronic technologies. However, heteroepitaxial growth of single crystal diamond remains limited, impeding integration and evolution of diamond-based technologies. Here, we directly bond single-crystal diamond membranes to a wide variety of materials including silicon, fused silica, sapphire, thermal oxide, and lithium niobate. Our bonding process combines customized membrane synthesis, transfer, and dry surface functionalization, allowing for minimal contamination while providing pathways for near unity yield and scalability. We generate bonded crystalline membranes with thickness as low as 10 nm, sub-nm interfacial regions, and nanometer-scale thickness variability over 200 by 200 $μm^2$ areas. We measure spin coherence times $T_2$ for nitrogen-vacancy centers in bonded membranes of up to 623(21) $μ$s, suitable for advanced quantum applications. We demonstrate multiple methods for integrating high quality factor nanophotonic cavities with the diamond heterostructures, highlighting the platform versatility in quantum photonic applications. Furthermore, we show that our ultra-thin diamond membranes are compatible with total internal reflection fluorescence (TIRF) microscopy, which enables interfacing coherent diamond quantum sensors with living cells while rejecting unwanted background luminescence. The processes demonstrated herein provide a full toolkit to synthesize heterogeneous diamond-based hybrid systems for quantum and electronic technologies.

physics.app-ph↗

arXiv2023

Engineering Spin Coherence in Core-Shell Diamond Nanocrystals

Diamond nanocrystals can harbor spin qubit sensors capable of probing the physical properties of biological systems with nanoscale spatial resolution. These diamond nanosensors can readily be delivered into intact cells and even living organisms. However, applications beyond current proof-of-principle experiments require a substantial increase in sensitivity, which is generally limited by surface-noise-induced spin dephasing and relaxation. In this work, we significantly reduce magnetic surface noise by engineering core-shell structures, which in combination with dynamical decoupling result in qubit coherence times (T2) ranging from 52us to 87us - a drastic improvement over the 1.1us to 35us seen in bare particles. This improvement in spin coherence, combined with an overall increase in particle fluorescence, corresponds to a two-order-of-magnitude reduction in integration time. Probing qubit dynamics at a single particle level, furthermore, reveals that the noise characteristics fundamentally change from a bath with spins that rearrange their spatial configuration during the course of an experiment to a more dilute static bath. The observed results shed light on the underlying mechanisms governing spin dephasing in diamond nanocrystals and offer an effective noise mitigation strategy based on engineered core-shell structures.

quant-ph↗

arXiv2022

Preparation of Metrological States in Dipolar-Interacting Spin Systems

Spin systems are an attractive candidate for quantum-enhanced metrology. Here we develop a variational method to generate metrological states in small dipolar-interacting ensembles with limited qubit controls and unknown spin locations. The generated states enable sensing beyond the standard quantum limit (SQL) and approaching the Heisenberg limit (HL). Depending on the circuit depth and the level of readout noise, the resulting states resemble Greenberger-Horne-Zeilinger (GHZ) states or Spin Squeezed States (SSS). Sensing beyond the SQL holds in the presence of finite spin polarization and a non-Markovian noise environment.

quant-ph↗

arXiv2021

Biocompatible surface functionalization architecture for a diamond quantum sensor

Quantum metrology enables some of the most precise measurements. In the life sciences, diamond-based quantum sensing has enabled a new class of biophysical sensors and diagnostic devices that are being investigated as a platform for cancer screening and ultra-sensitive immunoassays. However, a broader application in the life sciences based on nanoscale nuclear magnetic resonance spectroscopy has been hampered by the need to interface highly sensitive quantum bit (qubit) sensors with their biological targets. Here, we demonstrate a new approach that combines quantum engineering with single-molecule biophysics to immobilize individual proteins and DNA molecules on the surface of a bulk diamond crystal that hosts coherent nitrogen vacancy qubit sensors. Our thin (sub-5 nm) functionalization architecture provides precise control over protein adsorption density and results in near-surface qubit coherence approaching 100 μs. The developed architecture remains chemically stable under physiological conditions for over five days, making our technique compatible with most biophysical and biomedical applications.

quant-ph↗

arXiv2021

Materials challenges for quantum technologies based on color centers in diamond

Emerging quantum technologies require precise control over quantum systems of increasing complexity. Defects in diamond, particularly the negatively charged nitrogen-vacancy (NV) center, are a promising platform with the potential to enable technologies ranging from ultra-sensitive nanoscale quantum sensors, to quantum repeaters for long distance quantum networks, to simulators of complex dynamical processes in many-body quantum systems, to scalable quantum computers. While these advances are due in large part to the distinct material properties of diamond, the uniqueness of this material also presents difficulties, and there is a growing need for novel materials science techniques for characterization, growth, defect control, and fabrication dedicated to realizing quantum applications with diamond. In this review we identify and discuss the major materials science challenges and opportunities associated with diamond quantum technologies.

quant-ph↗

arXiv2019

Nanodiamond integration with photonic devices

We discuss the progress in integration of nanodiamonds with photonic devices for quantum optics applications. Experimental results in GaP, SiO2 and SiC-nanodiamond platforms show that various regimes of light and matter interaction can be achieved by engineering color center systems through hybrid approaches. We present our recent results on the growth of color center-rich nanodiamond on prefabricated 3C-SiC microdisk resonators. These hybrid devices achieve up to five-fold enhancement of diamond color center light emission and can be employed for integrated quantum photonics.

cond-mat.mes-hall↗

arXiv2018

Bright sub-20 nm cathodoluminescent nanoprobes for multicolor electron microscopy

Electron microscopy (EM) has been instrumental in our understanding of biological systems ranging from subcellular structures to complex organisms. Although EM reveals cellular morphology with nanoscale resolution, it does not provide information on the location of proteins within a cellular context. An EM-based bioimaging technology capable of localizing individual proteins and resolving protein-protein interactions with respect to cellular ultrastructure would provide important insights into the molecular biology of a cell. Here, we report on the development of luminescent nanoprobes potentially suitable for labeling biomolecules in a multicolor EM modality. In this approach, the labels are based on lanthanide-doped nanoparticles that emit light under electron excitation in a process known as cathodoluminescence (CL). Our results suggest that the optimization of nanoparticle composition, synthesis protocols and electron imaging conditions could enable high signal-to-noise localization of biomolecules with a sub-20-nm resolution, limited only by the nanoparticle size. In ensemble measurements, these luminescent labels exhibit narrow spectra of nine distinct colors that are characteristic of the corresponding rare-earth dopant type.

cond-mat.mtrl-sci↗

arXiv2017

Critical thermalization of a disordered dipolar spin system in diamond

Statistical mechanics underlies our understanding of macroscopic quantum systems. It is based on the assumption that out-of-equilibrium systems rapidly approach their equilibrium states, forgetting any information about their microscopic initial conditions. This fundamental paradigm is challenged by disordered systems, in which a slowdown or even absence of thermalization is expected. We report the observation of critical thermalization in a three dimensional ensemble of $\sim 10^6$ electronic spins coupled via dipolar interactions. By controlling the spin states of nitrogen vacancy color centers in diamond, we observe slow, sub-exponential relaxation dynamics and identify a regime of power-law decay with disorder-dependent exponents; this behavior is modified at late times owing to many-body interactions. These observations are quantitatively explained by a resonance counting theory that incorporates the effects of both disorder and interactions.

cond-mat.mes-hall↗

arXiv2016

Depolarization dynamics in a strongly interacting solid-state spin ensemble

We study the depolarization dynamics of a dense ensemble of dipolar interacting spins, associated with nitrogen-vacancy centers in diamond. We observe anomalously fast, density-dependent, and non-exponential spin relaxation. To explain these observations, we propose a microscopic model where an interplay of long-range interactions, disorder, and dissipation leads to predictions that are in quantitative agreement with both current and prior experimental results. Our results pave the way for controlled many-body experiments with long-lived and strongly interacting ensembles of solid-state spins.

quant-ph↗

arXiv2010

Scalable Architecture for a Room Temperature Solid-State Quantum Information Processor

The realization of a scalable quantum information processor has emerged over the past decade as one of the central challenges at the interface of fundamental science and engineering. Much progress has been made towards this goal. Indeed, quantum operations have been demonstrated on several trapped ion qubits, and other solid-state systems are approaching similar levels of control. Extending these techniques to achieve fault-tolerant operations in larger systems with more qubits remains an extremely challenging goal, in part, due to the substantial technical complexity of current implementations. Here, we propose and analyze an architecture for a scalable, solid-state quantum information processor capable of operating at or near room temperature. The architecture is applicable to realistic conditions, which include disorder and relevant decoherence mechanisms, and includes a hierarchy of control at successive length scales. Our approach is based upon recent experimental advances involving Nitrogen-Vacancy color centers in diamond and will provide fundamental insights into the physics of non-equilibrium many-body quantum systems. Additionally, the proposed architecture may greatly alleviate the stringent constraints, currently limiting the realization of scalable quantum processors.

quant-ph↗