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Peer-Review Record

Fabrication of PCDTBT Conductive Network via Phase Separation

Materials 2021, 14(17), 5071; https://doi.org/10.3390/ma14175071
by Jianwei Xu *, Zhiming Liu, Lei Jing and Jingbo Chen *
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Materials 2021, 14(17), 5071; https://doi.org/10.3390/ma14175071
Submission received: 4 August 2021 / Revised: 27 August 2021 / Accepted: 30 August 2021 / Published: 4 September 2021

Round 1

Reviewer 1 Report

Materials-1349030

Comments to the Editor

 Manuscript number Materials-1349030

 Fabrication of PCDTBT Conductive Network via  Phase Separation” presents the fabrication of a Poly[N-9''-hepta-decanyl-2,7-carbazole-alt-5-5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (PCDTBT) network consisting of aggregates and nanofibers in thin films, by phase separation of mixed PCDTBT and polyethylene glycol (PEG). The effect of blending conditions and processing conditions on the resulting phase separation morphologies of the blend films after a selectively washing procedure was studied.The phase separation structure transition from island to continuous structure occurred with the weight ratio of PCDTBT/PEG changed from 2:8 to 7:3. By increasing the solution concentration from 0.1 to 3.0 wt %, both PCDTBT height of aggregate and width of nanofiber increased. The film exhibited larger PCDTBT aggregate size, with the  increase of the molecular weight of PEG. The electrical characteristic of PCDTBT network was measured by conductive AFM.

If the manuscript would have some minor revision before publishing (editing mistakes, the names-legend of the figures are a little too loaded, maybe it’s better to explain its in the text), it will be interesting for the readers of the Materials.

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Reviewer 2 Report

Poly[N-9''-hepta-decanyl-2,7-carbazole-alt-5-5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)

CORRECT Poly[N-9′-heptadecanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)]

Abstract: (PCDTBT) is a stable semiconducting polymer with high rigidity of molecular chains, which makes it difficult to organize into ordered structure, affecting the device performance.

Page 2 Abstract: the electrical characteristic of PCDTBT CORRECT: the electrical characteristics of PCDTBT

Page 3: the orientation of micro- and nano-scale ordered structures also play an important role CORRECT the orientation of micro- and nano-scale ordered structures also plays an important role

Page 3: to control the ordered structures of conjugated polymers as well as its properties CORRECT: o control the ordered structures of conjugated polymers as well as their properties

Page 3: reduced combinatorial entropy of mixed two types of polymer chains CORRECT reduced combinatorial entropy of mixing two types of polymer chains

Page 4: PCDTBT were blend with a well-studied model polymers PEG CORRECT: In this work PCDTBT was blended with a well-studied model polymer PEG

Page 4: The phase separation morphologies conductivity of PCDTBT will be investigated by using conductive atomic force microscopy (CAFM). CORRECT: Conductivity of the phase separated morphologies of PCDTBT was investigated by using conductive atomic force microscopy (CAFM).

Page 9: AFM height images the films CORRECT: AFM height images of the films

Page 9: a network consisting PCDTBT aggregates and nanofibers is revealed, while no nanofiber (especially nanofiber) is observed in Figure 2f1. CORRECT: a network consisting of PCDTBT aggregates and nanofibers is revealed, while no fibers (especially nanofibers) are observed in Figure 2f1.

Page 9: the similar morphology as compare with Figure CORRECT: the similar morphology as compared with Figure

Page 9: indicating no PCDTBT nanofiber exists CORRECT: indicating that no PCDTBT nanofibers exist

Page 9: crystalline polymer with relative high flexibility than PCDTBT – CORRECT: rystalline polymer with relative higher flexibility than PCDTBT

Page 9: Figure 2g-k perform the AFM height images CORRECT: Figure 2g-k shows the AFM height images

Page 10: It is imperative to point out that, the length of nanofiber decreased CORRECT: It is imperative to point out that the length of nanofiber decreased

Page 10: reducing the diffusion distance REMARK: How do you define here the diffusion distance?

Page 11: PEG with different molecular weights is blended PCDTBT (Mn = 16.2 kg/mol) due to mobility and compatibility is sensitive to the molecular weight of polymer34. REMARK: Logically and grammatically incorrect sentence, please rewrite.

Page 11: Figure 3a-e show CORRECT: Figure 3a-e shows

Page 11: are exhibit PCDTBT network CORRECT:  exhibit PCDTBT networks

Page 12: With the increase of PEG molecular weight, the compatibility of two blend components decreases REMARK: is there any compatibility for low molecular weight PEG? The experimental work is based on phase separation driven by the  incompatibility of PCDTBT and PEG.

Page 12: phase separation morphology CORRECT: phase separated morphology

Page 12: Figure 3g and 3h show CORRECT: Figures 3g and 3h show

Page 12: The molecular weight dependent of the density and width of PCDTBT nanofiber CORRECT: The molecular weight dependencies of the density and width of PCDTBT nanofiber

Page 13: thermodynamically state CORRECT: thermodynamic state

Page 13: the phase separation structure transition from continuous structure to island was observed CORRECT the transition from continuous to island structure was observed

Page 13: The evaporation rate of the solvent decides the time-span available COREECT: The evaporation rate of the solvent decides about the time-span available

 

Page 14: few nanofibers are observed in the chloroform sample CORRECT: few nanofibers are observed in the sample obtained from chloroform solution

Page 14: during the stage of spin-coating shorten time for phase separation, hindering PCDTBT molecules self-assembling into nanofibers. CORRECT during the stage of spin-coating with shorter time available for phase separation, thus hindering PCDTBT molecules self-assembling into nanofibers.

Line 14: After removal of PEG by washing the samples in acetone CORRECT After removal of PEG from the films by washing it out with acetone

Page 15: and subsequently formed nanofibers and aggregates CORRECT: and subsequently nanofibers and aggregates are formed.

Page 15: after selectively remove CORRECT: after selective removal

Page 15: sea-island phase separation structure CORRECT: sea-island phase separated structure

Page 16: no nanofiber was observed CORRECT no nanofibers were observed

Page 16: the conductivity of blend film was proved by conductive AFM- CORRECT: the conductivity of PCDTBT structures obtained from the blend films was proved by conductive

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

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