Urea-formaldehyde Resin Derived P-doped Tungsten Carbide on N-carbon Sheets(P-W2C@NC)as All pH HER Catalyst

韩 苗苗
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Abstract

: Tungsten carbide has attracted extensive attention in the field of electrocatalytic hydrogen evolution due to its uni(|ue Pt like electronic structure and catalytic performance. He*teroatom doping and the constmction of nano­ materials with high specific suiface area are important strategies to further improve their propeilies. In this study, the heteroatom doped tungsten carbide with high specific surface area was prepared by controlled carbonization of u-rea formaldehyde resin with rich polar func tional groups as the substrate and polyoxonietalate clusters uniformly sup­ ported on its branched chain skeleton ( P - W - , C @ N C ) all j)H hydrogen evolution catalyst. The B K T specific surface area of the material is 136 • g _l. X R D , X P S , S E M and T E M results show that the catalyst is composed of tung­ sten carbide nanoparticles with phosphorus eloping and a thin nitrogen doped carbon layer coated oil the surface of tungsten carl)ide particles. In 0.5 mol/L sulfuric acid, 1 mol/L potassium hydroxide and 0.1 niol/L sulfuric acid buffer solution, the current density of 10 m A • c m " 2 can I)e achieved only by over potential of 83, 63 and 179 m V respectively, and this catalyst have long-term catalytic stability.
脲醛树脂衍生的n -碳片p掺杂碳化钨(P-W2C@NC)作为全pH HER催化剂
碳化钨由于具有类似铂的单一电子结构和催化性能,在电催化析氢领域引起了广泛的关注。杂原子掺杂和构建具有高比表面积的纳米材料是进一步提高其性能的重要策略。本研究以富极性官能团的脲醛树脂为底物,在支链骨架(P - W -, C @ N C)全j)H催化剂上均匀支撑聚氧乙酸酯簇,通过可控碳化法制备了具有高比表面积的杂原子掺杂碳化钨。材料的bkt比表面积为136•g_l。X R D、X P S、S E M和T E M结果表明,该催化剂由含磷的碳化钨纳米颗粒和包覆在碳化钨颗粒表面的薄氮掺杂碳层组成。在0.5 mol/L硫酸、1 mol/L氢氧化钾和0.1 niol/L硫酸缓冲溶液中,仅在超过电位分别为83、63和179 m V时,即可达到10 m A•c m“2”的电流密度,且该催化剂具有长期的催化稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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