Chien-Te Hsieh* and
Jen-Hao Hsueh
Department of Chemical Engineering and Materials Science, Yuan Ze University, Taoyuan 32003, Taiwan. E-mail: cthsieh@saturn.yzu.edu.tw; Fax: +886-3-4559373; Tel: +886-3-4638800 ext. 2577
First published on 7th October 2016
Correction for ‘Electrochemical exfoliation of graphene sheets from a natural graphite flask in the presence of sulfate ions at different temperatures’ by Chien-Te Hsieh et al., RSC Adv., 2016, 6, 64826–64831.
Several references were omitted from the reference section, and several citations in the Introduction section of the manuscript referred to the wrong references. The missing references have been added below; the reference numbers 1–4 refer to the new references given below, while the numbers 16, 17 and 34 refer to the references given in the original manuscript. The relevant sentences from the introduction are given below with the correct referencing:
The EE of graphite into GN with one or a few stacks of graphene-like sheets could be achieved using different types of electrolytes such as LiCl in propylene carbonate (PC),16 (NH4)2SO4 aqueous solution,17 LiOH molten salt,1 LiClO4 in PC,2 LiCl in dimethyl sulfoxide,3 and H2SO4 aqueous solution.34,4
This is because SO42− ions tend to intercalate defective sites at edges or grain boundaries of graphite, originated from the electrolysis of water.34 This superior efficiency can be attributed to a lower reduction potential of SO42− ions (+0.20 V) to enable release of SO2 gas and anion depolarization,17,4 causing the widening of interlayer distance of graphite.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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