Extrinsic cation selectivity of 2D membranes

From a systematic study of the concentration driven diffusion of positive and negative ions across porous 2D membranes of graphene and hexagonal boron nitride (h-BN), we prove their cation selectivity. Using the current–voltage characteristics of graphene and h-BN monolayers separating reservoirs of...

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Main Authors: Walker, MI, Ubych, K, Saraswat, V, Chalklen, EA, Braeuninger-Weimer, P, Caneva, S, Weatherup, RS, Hofmann, S, Keyser, UF
Format: Journal article
Language:English
Published: American Chemical Society 2017
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author Walker, MI
Ubych, K
Saraswat, V
Chalklen, EA
Braeuninger-Weimer, P
Caneva, S
Weatherup, RS
Hofmann, S
Keyser, UF
author_facet Walker, MI
Ubych, K
Saraswat, V
Chalklen, EA
Braeuninger-Weimer, P
Caneva, S
Weatherup, RS
Hofmann, S
Keyser, UF
author_sort Walker, MI
collection OXFORD
description From a systematic study of the concentration driven diffusion of positive and negative ions across porous 2D membranes of graphene and hexagonal boron nitride (h-BN), we prove their cation selectivity. Using the current–voltage characteristics of graphene and h-BN monolayers separating reservoirs of different salt concentrations, we calculate the reversal potential as a measure of selectivity. We tune the Debye screening length by exchanging the salt concentrations and demonstrate that negative surface charge gives rise to cation selectivity. Surprisingly, h-BN and graphene membranes show similar characteristics, strongly suggesting a common origin of selectivity in aqueous solvents. For the first time, we demonstrate that the cation flux can be increased by using ozone to create additional pores in graphene while maintaining excellent selectivity. We discuss opportunities to exploit our scalable method to use 2D membranes for applications including osmotic power conversion.
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spelling oxford-uuid:7f47c788-cd72-4425-8f33-46353fe8bdb72022-03-26T21:16:07ZExtrinsic cation selectivity of 2D membranesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7f47c788-cd72-4425-8f33-46353fe8bdb7EnglishSymplectic ElementsAmerican Chemical Society2017Walker, MIUbych, KSaraswat, VChalklen, EABraeuninger-Weimer, PCaneva, SWeatherup, RSHofmann, SKeyser, UFFrom a systematic study of the concentration driven diffusion of positive and negative ions across porous 2D membranes of graphene and hexagonal boron nitride (h-BN), we prove their cation selectivity. Using the current–voltage characteristics of graphene and h-BN monolayers separating reservoirs of different salt concentrations, we calculate the reversal potential as a measure of selectivity. We tune the Debye screening length by exchanging the salt concentrations and demonstrate that negative surface charge gives rise to cation selectivity. Surprisingly, h-BN and graphene membranes show similar characteristics, strongly suggesting a common origin of selectivity in aqueous solvents. For the first time, we demonstrate that the cation flux can be increased by using ozone to create additional pores in graphene while maintaining excellent selectivity. We discuss opportunities to exploit our scalable method to use 2D membranes for applications including osmotic power conversion.
spellingShingle Walker, MI
Ubych, K
Saraswat, V
Chalklen, EA
Braeuninger-Weimer, P
Caneva, S
Weatherup, RS
Hofmann, S
Keyser, UF
Extrinsic cation selectivity of 2D membranes
title Extrinsic cation selectivity of 2D membranes
title_full Extrinsic cation selectivity of 2D membranes
title_fullStr Extrinsic cation selectivity of 2D membranes
title_full_unstemmed Extrinsic cation selectivity of 2D membranes
title_short Extrinsic cation selectivity of 2D membranes
title_sort extrinsic cation selectivity of 2d membranes
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