4.8 Article

Direct observation of electron emission from grain boundaries in CVD diamond by PeakForce-controlled tunnelling atomic force microscopy

Journal

CARBON
Volume 94, Issue -, Pages 386-395

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2015.06.082

Keywords

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Funding

  1. EPSRC [EP/H043292/1]
  2. Research Foundation - Flanders (FWO) [G.0456.12]
  3. EPSRC [EP/H043292/1, EP/K035746/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/K035746/1, 1229263, EP/H043292/1] Funding Source: researchfish

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A detailed investigation of electron emission from a set of chemical vapour deposited (CVD) diamond films is reported using high-resolution PeakForce-controlled tunnelling atomic force microscopy (PF-TUNA). Electron field emission originates preferentially from the grain boundaries in low-conductivity polycrystalline diamond samples, and not from the top of features or sharp edges. Samples with smaller grains and more grain boundaries, such as nanocrystalline diamond, produce a higher emission current over a more uniform area than diamond samples with larger grain size. Light doping with N, B or P increases the grain conductivity, with the result that the emitting grain-boundary sites become broader as the emission begins to creep up the grain sidewalls. For heavy B doping, where the grains are now more conducting than the grain boundaries, emission comes from both the grain boundaries and the grains almost equally. Lightly P-doped diamond samples show emission from step-edges on the (111) surfaces. Emission intensity was time dependent, with the measured current dropping to similar to 10% of its initial value similar to 30 h after removal from the CVD chamber. This decrease is ascribed to the build-up of adsorbates on the surface along with an increase in the surface conductivity due to surface transfer doping. (C) 2015 The Authors. Published by Elsevier Ltd.

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