journal article·2016-04-07

Photoelectrochemical Behavior of n-Type GaAs(100) Electrodes Coated by a Single Layer of Graphene

Fan Yang, Adam C. Nielander, Ronald L. Grimm, Nathan S. Lewis

The Journal of Physical Chemistry C· Volume 120· Issue 13
Publisher page

Abstract

The photoelectrochemical behavior of n-type GaAs(100) electrodes coated with a single layer of graphene was compared with the behavior of bare, freshly etched n-type GaAs(100) electrodes, both for electrodes in contact with an aqueous solution containing K 3 [Fe(CN) 6 ]/K 4 [Fe(CN) 6 ] and for electrodes in contact with nonaqueous solutions containing a series of one-electron redox couples selected such that the Nernstian solution potentials spanned a range greater than 1 V. Under simulated 1 Sun illumination, the graphene-coated electrodes produced a short-circuit photocurrent density of 20 mA cm –2 for up to 8 h of continuous operation in nonaqueous electrolytes (H 2 O concentration 0.1%, v/v), while, under the same conditions, the unprotected n-GaAs electrodes showed a rapid decay of the photocurrent density within ∼400 s. Although the graphene monolayers enhanced the stability of n-GaAs photoanodes in nonaqueous electrolytes, the graphene did not fully protect photoanodes operated in contact with Fe(CN) 6 3–/4– (aq) from corrosion. The dependence of the open-circuit voltage measured for graphene-coated n-GaAs photoanodes on the Nernstian potential of the solution was effectively identical to that of freshly etched n-GaAs photoanodes, indicating that addition of the graphene layer did not introduce significant pinning of the Fermi level of GaAs beyond the Fermi-level pinning attributable to mid-gap and solution-derived charge-carrier trap states previously observed at GaAs/liquid junctions.
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Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Nanowire Synthesis and Applications · Graphene research and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States

Funding

Division of Chemistry · Gordon and Betty Moore Foundation · National Science Foundation

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