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Co,N-Codoped porous vanadium nitride nanoplates as superior bifunctional electrocatalysts for hydrogen evolution and oxygen reduction reactions

机译:有限公司N-Codoped多孔氮化钒nanoplates优越的双官能electrocatalysts为氢进化和氧还原反应

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Developing efficient and low-cost bifunctional electrocatalysts as candidates for Pt-based materials to satisfy commercial applications in the hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR) is still very challenging. Herein, we show that Co,N-codoped porous vanadium nitride (VCoN) nanoplates are successfully synthesized via a simple one-step pyrolysis protocol without the use of NH3 gas. We also demonstrate that the crystallization, surface chemical state and porosity of vanadium nitride are well modulated by inventively using Co dopants as structural inducers. The resulting VCoN material exhibits an excellent catalytic activity towards the HER in alkaline media, with an extremely low onset potential of -0.03 V, an overpotential of 179 mV at 10 mA cm(-2), and a remarkable durability for over 100 h. Moreover, it shows a superior ORR performance, which compares favorably with commercial 20% Pt/C, exhibiting an onset potential of similar to 1.02 V, a half-wave potential of similar to 0.91 V and a weak potential shift (-5 mV) after 2000 cycles at 1600 rpm in 0.1 M KOH. Such excellent electrocatalytic performance primarily contributes to the unique structural features of the heteroatom N (pyrrolic and graphitic N) and Co codoping in favor of improving the electrical conductivity and the high porosity contributing to exposing numerous catalytic active sites.
机译:开发高效、低成本的双官能electrocatalysts Pt-based候选人材料以满足商业应用(她)和氧氢进化反应还原反应(ORR)仍然非常具有挑战性的。多孔氮化钒(VCoN) nanoplates通过一个简单的一步法成功地合成热解协议不使用NH3气体。也表明,结晶,表面化学状态和钒的孔隙度氮化调制通过率先的使用Co掺杂物结构诱导物。VCoN展示一个优秀的催化材料在碱性媒体活动向她,-0.03 V的极低的爆发潜力过电压的马179 mV在10厘米(2),和一个此外,卓越的耐久性了100 h。它显示了一个奥尔性能优越,Pt / C优于商业20%,表现出一个类似于1.02的爆发潜力V, 0.91 V和类似的半波电位疲软的潜在转移2000次后(5号)在0.1 KOH 1600 rpm。electrocatalytic性能主要独特的结构特点杂原子N (pyrrolic和石墨N)公司共掺的改善电电导率和高孔隙度的贡献暴露了许多催化活性位点。

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