Bimetallic Ni–Pt nanoparticles immobilized on mesoporous N-doped carbon as a highly efficient catalyst for complete hydrogen evolution from hydrazine borane. Issue 27 (2nd July 2020)

• Record Type: Journal Article
• Authors: Wang, Wei; Hong, Xiaoling; Yao, Qilu; Lu, Zhang-Hui
• Is Part Of: Journal of materials chemistry. Volume 8:Issue 27(2020)
• Page Start: 13694
• Page End: 13701
• Publication Date: 2020-07-02
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d0ta05322h
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : NiPt NPs immobilized on mesoporous N-doped carbon have been facilely synthesized for efficient and complete hydrogen generation from N2 H4 BH3 solution at room temperature. Abstract : In this work, mesoporous N-doped carbon (MNC) materials have been successfully prepared by a nanocasting route using SBA-15 as the template and ethylenediamine (EDA) and carbon tetrachloride (CTC) as carbon nitride precursors. The specific surface area and pore size of the MNC, as well as the C/N content are strongly dependent on the pyrolysis temperature. The as-obtained MNC-supported NiPt nanoparticles (NPs) were used as efficient catalysts toward complete dehydrogenation of hydrazine borane (HB) in alkaline solution at room temperature. Among all the catalysts investigated, the Ni60 Pt40 /MNC-800 nanocomposites (NCs) show the highest catalytic activity and 100% hydrogen selectivity. The total turnover frequency (TOF) of Ni60 Pt40 /MNC-800 NCs reached 1111 h −1 at room temperature, the highest activity among all catalysts reported to date. The superior catalytic properties were possibly a result of the electronic interaction between Ni and Pt, the synergistic effects of the NiPt NPs and MNC support, the ordered pore structure for free mass transfer and the small-sized metal NPs.