• 文献标题:   Self-Assembled NbOPO4 Nanosheet/Reduced Graphene Oxide Heterostructure for Capacitive Desalination
  • 文献类型:   Article
  • 作  者:   SAFAEI J, MASHKANI SMH, TIAN H, YE CC, XIONG P, WANG GX
  • 作者关键词:   2d material, interface coupling, heterostructure, capacitive deionization, water desalination
  • 出版物名称:   ACS APPLIED NANO MATERIALS
  • ISSN:  
  • 通讯作者地址:  
  • 被引频次:   6
  • DOI:   10.1021/acsanm.1c03180
  • 出版年:   2021

▎ 摘  要

Capacitive deionization (CDI) is a promising and energy-efficient technology for desalination. The development of high-performance capacitive electrodes is essential for enhancing the CDI properties for practical applications. Here, a 2D heterostructure was rationally designed and synthesized by face-to-face restacking of NbOPO4 nanosheets and reduced graphene oxide (rGO) via an electrostatic self-assembly process. The as-prepared 2D NbOPO4/rGO heterostructure achieved an excellent ion storage capacity, electronic conductivity, and unimpeded ion kinetics. When applied as electrodes for CDI, the 2D NbOPO4/rGO heterostructure delivered a high specific capacitance of 258.3 F g(-1) and an electrosorption capacity of 73 mg g(-1) for NaCl solution of 10 000 mg L-1 at an applied voltage of 1.2 V, which is more than five times larger than that of activated carbon. The heterostructure electrode also showed high desalination stability for up to 50 adsorption/desorption cycles. The high CDI performance is attributed to the strong 2D/2D coupling between NbOPO4 nanosheets and rGO. The strong 2D/2D coupling reduced the charge transfer resistance, affirmed via the electrochemical impedance spectroscopy technique, attesting to the enhanced charge transportation across the heterointer-face. The robust 2D/2D coupling was affirmed via the uniform and identical Raman shifts at various random regions, and larger XPS binding energy shifts for the self-assembled NbOPO4/rGO heterostructure. This work demonstrated the potential of self-assembled nanoheterostructures for water desalination via capacitive deionization.