Bifunctional networked Ag/AgPd core/shell nanowires for the highly efficient dehydrogenation of formic acid and subsequent reduction of nitrate and nitrite in water. Issue 11 (27th February 2018)

• Record Type: Journal Article
• Authors: Liu, Hu; Liu, Xinyang; Yu, Yongsheng; Yang, Weiwei; Li, Ji; Feng, Ming; Li, Haibo
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 11(2018)
• Page Start: 4611
• Page End: 4616
• Publication Date: 2018-02-27
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8ta00600h
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Herein, we report the one-pot synthesis of networked Ag/AgPd core/shell nanowires (CS-NWs) via seed-mediated growth in polyol solution. Abstract : Nitrate (NO3 − ) and nitrite (NO2 − ) pollution in water has increasingly become a serious environmental concern. The catalytic reduction of NO3 − and NO2 − to harmless N2 by a reducing agent is considered to be one of the most promising methods to remove NO3 − and NO2 − from water. Herein, we report the one-pot synthesis of networked Ag/AgPd core/shell nanowires (CS-NWs) via seed-mediated growth in polyol solution. The shell thickness of the networked Ag/AgPd CS-NWs can be readily controlled by tuning the amount of precursors. The networked Ag/AgPd CS-NWs with a 0.9 nm shell thickness exhibited the highest activity towards the dehydrogenation catalysis of FA with an initial TOF of 1400 h −1 at 50 °C, and the highest selectivity for the catalysis of NO3 − and NO2 − to N2 in water and at room temperature. Their enhanced bifunctional catalytic performance could be attributed to more efficient electron transfer from PVPI and Ag to Pd. This work demonstrates a new way to prepare bifunctional nanocatalysts for the removal of NO3 − and NO2 − from water using FA as the in situ hydrogen source.