# Graphene oxide adsorptive power from better to more via an enhanced   route in perspective

**Authors:** Sun Ling

arXiv: 1705.00523 · 2017-05-02

## TL;DR

This paper explores how the adsorptive performance of graphene oxide can be significantly improved by orienting and manipulating its surface functional groups, offering a promising route for water decontamination.

## Contribution

It introduces a novel approach of surface functional group manipulation on graphene oxide to enhance its adsorption capabilities for water purification.

## Key findings

- Enhanced adsorption performance through functional group orientation.
- Potential for combined adsorption and in-situ surface modification.
- Insights into the relationship between functional group distribution and adsorption efficiency.

## Abstract

Adsorption is one important way applied to water decontamination, where carbon is commonly used as highly effective absorbent. Carbon of different morphologies and structures normally demonstrate distinct capabilities to adsorption-typed decontaminations. Graphene oxide is regarded as the oxidative derivative of graphene, maintaining its 2D morphology-featuring structure while location-dependently immobilized with a large amount of various oxygen-involving functional moieties on both sides. Free-standing graphene oxide tends to fully unfold in water and behave in macromolecular-like Brownian motion. Therefore, high-performance adsorption occurs during the process of interacting with large amount of sorbates, during which an unevenness of effective adsorptive site distribution turns out for targeted matter due to functional group-to-sorbate interaction mechanism differentiation as well as groups'inherent location specifications. Thus, oriented manipulation of surficial functional moieties and their site distribution is potentially a way to further enhance the adsorptive performances, and this could go even better if considering combining adsorption and an in-situ manipulation at the same time.

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Source: https://tomesphere.com/paper/1705.00523