Journal Reference
Advanced Functional Materials, Volume 25, Issue 25, pages 3899–3906, 2015.
Sheng Han1, Yunlong Feng1, Fan Zhang2,*, Chongqing Yang2, Zhaoquan Yao2,Wuxue Zhao2, Feng Qiu1,2, Lingyun Yang3, Yefeng Yao3, Xiaodong Zhuang2,*, Xinliang Feng2,4
[expand title=”Show Affiliations”]- School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai, P. R. China
- School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, P. R. China
- Physics Department & Shanghai Key Laboratory of Magnetic Resonance, East China Normal University, Shanghai, P. R. China
- Technische Universität Dresden, Dresden, Germany
Abstract
One novel phosphorus-containing porous polymer (HC-TVP), was high efficiently prepared from tris(4-vinylphenyl)phosphane by radical polymerization, which can be easily ionized to form ionic porous polymer under the treatment of hydrogen iodide. Upon ionic exchange, transition metal-containing anions, such as tetrathiomolybdate (MoS42-), and hexacyanoferrate (Fe(CN)63-), were successfuly loaded into the framework of the porous polymer to replace the original iodide anions and form metal-coordinated anions contained polymer frameworks (HT-Mets, Met=Mo, Fe). After pyrolysis under hydrogen atmosphere, HT-Mets were efficiently converted to metal phosphide-embedded porous carbons (MetP@PCs, Met=Mo, Fe) on a large scale. This approach provides a convenient pathway to the controlled preparation of metal phosphide-loaded porous carbon composites. The as-made MetP@PCs exhibits superior electrocatalytic activity for hydrogen evolution reaction (HER) under acidic condition. Of these, MoP@PC with a low loading of 0.24 mgcm−2 (on glass carbon electrode) afforded an iR-corrected current density of up to 10 mA cm−2 at 51 mV vs. RHE and a very low Tafel slope of 45 mVdec−1, in rotating disk measurements under N2 saturated condition.
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