Controlled synthesis of MnO2@TiO2 hybrid nanotube arrays with enhanced oxygen evolution reaction performance. (2nd August 2018)

• Record Type: Journal Article
• Authors: Li, Xia; Zhang, Manru; Zhang, Yong; Yu, Cuiping; Qi, Wentao; Cui, Jiewu; Wang, Yan; Qin, Yongqiang; Liu, Jiaqin; Shu, Xia; Chen, Ying; Xie, Ting; Wu, Yucheng
• Is Part Of: International journal of hydrogen energy. Volume 43:Number 31(2018)
• Page Start: 14369
• Page End: 14378
• Publication Date: 2018-08-02
• Subjects: Hybrid nanotubes -- TiO2 -- MnO2 -- Oxygen evolution reaction -- Chemical bath deposition; Hydrogen as fuel -- Periodicals; Hydrogène (Combustible) -- Périodiques; Hydrogen as fuel; Periodicals; 665.81
• DOI: 10.1016/j.ijhydene.2018.06.027
• Languages: English
• ISSNs: 0360-3199

Abstract

Abstract: A novel tube-in-tube nanostructure of MnO2 @ TiO2 hybrid arrays has been obtained by a facile and controllable chemical bath deposition method. Scrutiny on the hybrid arrays indicates that the chemical bath deposition method favors the growth of the MnO2 nanotubes with different diameter which can modulate the oxygen evolution reaction (OER) activity as well as bandgap width of the hybrid. In terms of OER activity, onset potential ( E s ) shifts negatively from 0.698 V (vs.Ag/AgCl) of pristine titania nanotube arrays (TNAs) to 0.501 V of the hybrid loaded with 26.6%wt MnO2, and the current density on the hybrid electrode can be significantly enhanced up to 20.87 mA/cm 2, almost 97 times higher than that on TNAs electrode (0.214 mA/cm 2 ). Optical absorption measurement suggests that the bandgap width ( E g ) can be tuned by loading MnO2 onto the TNAs implying interaction between the MnO2 and TNAs. The MnO2 @TiO2 hybrid nanotube arrays may find promising potential in electrochemical water splitting, photocatalysis, thermocatalysis and other sustainable energy applications. Graphical abstract: Image 1 Highlights: MnO2 @TiO2 hybrid nanotubes have been obtained by chemical bath deposition. Oxygen evolution reaction activity of the hybrid is enhanced by loading MnO2 . The j 1v of the hybrids reaches 97 times higher than that of the TiO2 electrode. Bandgap width of the hybrid can be modulated by adjusting MnO2 loadings.