Extremely high negative electron affinity of diamond via magnesium adsorption
Kane M. O'Donnell, Mark T. Edmonds, Anton Tadich, Lars Thomsen,, Alastair Stacey, Alex Schenk, Chris I. Pakes, Lothar Ley

TL;DR
This study demonstrates a novel method to achieve the largest negative electron affinity on diamond surfaces through magnesium adsorption, which remains stable under various environmental conditions.
Contribution
It introduces magnesium adsorption as an effective way to induce and stabilize high negative electron affinity on diamond surfaces without high-temperature activation.
Findings
Achieved NEA of up to -2.01 eV on diamond (100) surface.
Magnesium-adsorbed diamond surfaces remain NEA after environmental exposure.
Mg adsorption differs from Li in surface chemistry and activation requirements.
Abstract
We report large negative electron affinity (NEA) on diamond (100) using magnesium adsorption on a previously oxygen-terminated surface. The measured NEA is up to eV, the largest reported negative electron affinity to date. Despite the expected close relationship between the surface chemistry of Mg and Li species on oxygen-terminated diamond, we observe differences in the adsorption properties between the two. Most importantly, a high-temperature annealing step is not required to activate the Mg-adsorbed surface to a state of negative electron affinity. Diamond surfaces prepared by this procedure continue to possess negative electron affinity after exposure to high temperatures, air and even immersion in water.
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Taxonomy
TopicsDiamond and Carbon-based Materials Research · Electronic and Structural Properties of Oxides · Electron and X-Ray Spectroscopy Techniques
