TY - JOUR
T1 - Scalable and controlled creation of nanoholes in graphene by microwave-assisted chemical etching for improved electrochemical properties
AU - Wang, Dini
AU - Dai, Rui
AU - Zhang, Xing
AU - Liu, Lei
AU - Zhuang, Houlong
AU - Lu, Yongfeng
AU - Wang, Yan
AU - Liao, Yiliang
AU - Nian, Qiong
N1 - Funding Information:
This study is partially supported by Arizona State University startup funds, NSF grant CMMI-1825576. We acknowledge the use of facilities within the Eyring Materials Center at Arizona State University supported in part by NNCI-ECCS-1542160. This research also used computational resources of the Texas Advanced Computing Center under contract no. TG-DMR170070. We also appreciate the assistance of Dr. Q. H. Wang and her group members in Raman spectroscopy study.
Funding Information:
This study is partially supported by Arizona State University startup funds, NSF grant CMMI-1825576 . We acknowledge the use of facilities within the Eyring Materials Center at Arizona State University supported in part by NNCI-ECCS-1542160 . This research also used computational resources of the Texas Advanced Computing Center under contract no. TG-DMR170070. We also appreciate the assistance of Dr. Q. H. Wang and her group members in Raman spectroscopy study.
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/5
Y1 - 2020/5
N2 - Nanoholes on the basal plane of graphene can provide abundant mass transport channels and chemically active sites for enhancing the electrochemical performance. However, current thermal chemical etching processes to manufacture these nanoholes commonly suffer from insufficient process efficiency, scalability and controllability, due to the conventional bulk heating strategy lacks capability to promote the etching reactions. To address this issue, a novel process is developed using microwave irradiation to promote and control the chemical etching of graphene. In this process, the microwave can induce a selective heating of graphene in the liquid solution and then facilitate the etching reactions occurring on the graphene-etchant interface. Applying this strategy, a remarkable reduction of processing time from hour-scale to minute-scale compared to the conventional approaches have been achieved with the control of the population and area percentage of nanoholes on the graphene basal plane. Density functional theory and molecular dynamics simulations revealed that the formation of nanoholes originated from the cyclic etchant oxidation process occurring at the edge-sites atoms around pretreated vacancies on graphene basal plane. The obtained holey graphene oxide sheets exhibit excellent capacitive performance and electrochemical catalytic activity due to the improvements in the accessible surface area, ion diffusion, and heterogeneous charge transfer.
AB - Nanoholes on the basal plane of graphene can provide abundant mass transport channels and chemically active sites for enhancing the electrochemical performance. However, current thermal chemical etching processes to manufacture these nanoholes commonly suffer from insufficient process efficiency, scalability and controllability, due to the conventional bulk heating strategy lacks capability to promote the etching reactions. To address this issue, a novel process is developed using microwave irradiation to promote and control the chemical etching of graphene. In this process, the microwave can induce a selective heating of graphene in the liquid solution and then facilitate the etching reactions occurring on the graphene-etchant interface. Applying this strategy, a remarkable reduction of processing time from hour-scale to minute-scale compared to the conventional approaches have been achieved with the control of the population and area percentage of nanoholes on the graphene basal plane. Density functional theory and molecular dynamics simulations revealed that the formation of nanoholes originated from the cyclic etchant oxidation process occurring at the edge-sites atoms around pretreated vacancies on graphene basal plane. The obtained holey graphene oxide sheets exhibit excellent capacitive performance and electrochemical catalytic activity due to the improvements in the accessible surface area, ion diffusion, and heterogeneous charge transfer.
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U2 - 10.1016/j.carbon.2020.01.076
DO - 10.1016/j.carbon.2020.01.076
M3 - Article
AN - SCOPUS:85079353318
SN - 0008-6223
VL - 161
SP - 880
EP - 891
JO - Carbon
JF - Carbon
ER -