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Quantum Diamonds at the Beach: Chemical Insights into Silica Growth on Nanoscale Diamond using Multimodal Characterization and Simulation.
Sandoval, Perla J; Lopez, Karen; Arreola, Andres; Len, Anida; Basravi, Nedah; Yamaguchi, Pomaikaimaikalani; Kawamura, Rina; Stokes, Camron X; Melendrez, Cynthia; Simpson, Davida; Lee, Sang-Jun; Titus, Charles James; Altoe, Virginia; Sainio, Sami; Nordlund, Dennis; Irwin, Kent; Wolcott, Abraham.
Afiliação
  • Sandoval PJ; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Lopez K; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Arreola A; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Len A; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Basravi N; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Yamaguchi P; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Kawamura R; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Stokes CX; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Melendrez C; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Simpson D; Department of Chemistry, San José State University, 1 Washington Square, San José, California 95192, United States.
  • Lee SJ; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sandhill Road, Menlo Park, California 94025, United States.
  • Titus CJ; Department of Physics, Stanford University, 382 Via Pueblo Mall, Palo Alto, California 94025, United States.
  • Altoe V; The Molecular Foundry, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, California 94720, United States.
  • Sainio S; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sandhill Road, Menlo Park, California 94025, United States.
  • Nordlund D; Microelectronics Research Unit, University of Oulu, Pentti Kaiteran katu 1, Linnanmaa, P.O. Box 4500, Oulu 90014, Finland.
  • Irwin K; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sandhill Road, Menlo Park, California 94025, United States.
  • Wolcott A; Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, 2575 Sandhill Road, Menlo Park, California 94025, United States.
ACS Nanosci Au ; 3(6): 462-474, 2023 Dec 20.
Article em En | MEDLINE | ID: mdl-38144705
ABSTRACT
Surface chemistry of materials that host quantum bits such as diamond is an important avenue of exploration as quantum computation and quantum sensing platforms mature. Interfacing diamond in general and nanoscale diamond (ND) in particular with silica is a potential route to integrate room temperature quantum bits into photonic devices, fiber optics, cells, or tissues with flexible functionalization chemistry. While silica growth on ND cores has been used successfully for quantum sensing and biolabeling, the surface mechanism to initiate growth was unknown. This report describes the surface chemistry responsible for silica bond formation on diamond and uses X-ray absorption spectroscopy (XAS) to probe the diamond surface chemistry and its electronic structure with increasing silica thickness. A modified Stöber (Cigler) method was used to synthesize 2-35 nm thick shells of SiO2 onto carboxylic acid-rich ND cores. The diamond morphology, surface, and electronic structure were characterized by overlapping techniques including electron microscopy. Importantly, we discovered that SiO2 growth on carboxylated NDs eliminates the presence of carboxylic acids and that basic ethanolic solutions convert the ND surface to an alcohol-rich surface prior to silica growth. The data supports a mechanism that alcohols on the ND surface generate silyl-ether (ND-O-Si-(OH)3) bonds due to rehydroxylation by ammonium hydroxide in ethanol. The suppression of the diamond electronic structure as a function of SiO2 thickness was observed for the first time, and a maximum probing depth of ∼14 nm was calculated. XAS spectra based on the Auger electron escape depth was modeled using the NIST database for the Simulation of Electron Spectra for Surface Analysis (SESSA) to support our experimental results. Additionally, resonant inelastic X-ray scattering (RIXS) maps produced by the transition edge sensor reinforces the chemical analysis provided by XAS. Researchers using diamond or high-pressure high temperature (HPHT) NDs and other exotic materials (e.g., silicon carbide or cubic-boron nitride) for quantum sensing applications may exploit these results to design new layered or core-shell quantum sensors by forming covalent bonds via surface alcohol groups.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Nanosci Au Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Nanosci Au Ano de publicação: 2023 Tipo de documento: Article