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电镀法制备Pt/TiO_(2)纳米管电极及其电催化析氢性能 被引量:6

Pt/TiO_(2) Nanotubes Electrode:Preparation by Electroplating Method and Electrocatalytic Hydrogen Evolution Performance
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摘要 采用阳极氧化法制备得到锐钛矿型二氧化钛(TiO_(2))纳米管阵列,在其表面通过电镀法沉积Pt,得到了低铂的Pt/TiO_(2)纳米管电极(Pt/TiO_(2)‑NTs)。通过扫描电子显微镜和透射电子显微镜对其进行形貌表征后发现,Pt较为均匀地分布于TiO_(2)纳米管阵列中。进一步的电催化析氢结果表明,Pb/TiO_(2)‑NTs在10 mA·cm^(-2)时,过电位为0.079 V,塔菲尔斜率为42.7 mV·dec-1,较Pt/TiO_(2)致密膜电极(Pt/TiO_(2)‑F)以及商业Pt/C催化剂显示了更为优异的催化活性。同时,在长循环稳定性测试(3000个周期)中,Pb/TiO_(2)‑NTs相较于上述2种对比电极显示了更为优异的稳定性。 Here,Pt modified anatase‑type titanium dioxide(TiO_(2))nanotube arrays were prepared by electroplating method for a low‑platinum Pt/TiO_(2) nanotubes electrode(Pt/TiO_(2)‑NTs).By contrast,we fixed Pt on TiO_(2) dense film by the same procedure as a control sample(Pt/TiO_(2)‑F).The scanning electron microscopy and transmission electron microscopy observation showed that Pt nanoparticles were distributed uniformly in nanotube arrays,and Pt/TiO_(2)‑NTs showed a higher efficiency in electrocatalytic hydrogen evolution compared with Pt/TiO_(2)‑F and commercial Pt/C catalyst,in which the overpotential of Pt/TiO_(2)‑NTs was 0.079 V,the Tafel slope was 42.7 mV·dec-1 at 10 mA·cm^(-2).The catalytic activity of 3000 cycles duration stability test results showed that Pt/TiO_(2)‑NTs exhibited excellent stability compared with the above contrast electrodes.
作者 吴安冉 陈言慧 王心心 周文元 何佳伟 王金淑 李洪义 WU An‑Ran;CHEN Yan‑Hui;WANG Xin‑Xin;ZHOU Wen‑Yuan;HE Jia‑Wei;WANG Jin‑Shu;LI Hong‑Yi(Faculty of Materials and Manufacturing,Beijing University of Technology,Beijing 100124,China)
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2022年第2期227-236,共10页 Chinese Journal of Inorganic Chemistry
基金 北京市长城学者培养计划项目(No.CIT&TCD20190307) 北京市自然科学基金(No.Z210016) 北京市百千万人才计划项目(No.2020016)资助。
关键词 TiO_(2)纳米管载体 电镀 铂基催化剂 电催化析氢 TiO_(2)nanotubes carrier electroplating platinum‑based catalyst electrocatalytic hydrogen evolution
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  • 1O. J. Curnick, B. G. Pollet, P. M. Mendes, RSC Adv., 2012, 2, 8368-8374.
  • 2V. R. Stamenkovic, B. S. Mun, M. Arenz, K. J. Mayrhofer, C. A. Lucas, G. Wang, P. N. Ross, N. M. Markovic, Nat. Mater., 2007, 6, 241-247.
  • 3Y. Garsany, I. L. Singer, K. E. Swider-Lyons, J. Electroanal. Chem., 2011, 662, 396-406.
  • 4U. A. Paulus, T. J. Schmidt, H. A. Gasteiger, R. J. Behm, J. Electroanal. Chem., 2001, 495, 134-145.
  • 5K. J. J. Mayrhofer, D. Strmcnik, B. B. Blizanac, V. Stamenkovic, M. Arenz, N. M. Markovic, Electrochim. Acta, 2008, 53, 3181-3188.
  • 6G. Yannick, O. A. Baturina, K. E. Swider-Lyons, S. S. Kocha, Anal. Chem., 2010, 82, 6321-6328.
  • 7Y. Garsany, A. Epshteyn, A. P. Purdy, K. L. More, K. E. Swider-Lyons, J Phys. Chem. Lett., 2010, 1, 1977-1981.
  • 8C. Chen, Y. J. Kang, Z. Y. Huo, Z. W. Zhu, W. Y. Huang, H. L. Xin, J. D. Snyder, D. Li, J. A. Herron, M. Mavrikakis, M. Chi, K. L. More, Y. D. Li, N. M. Markovic, G. A. Somorjai, P. Yang, V. R. Stamenkovic, Science, 2014, 343, 1339-1343.
  • 9C. H. Cui, L. Gan, M. Heggen, S. Rudi, P. Strasser, Nat. Mater., 2013, 12, 765-771.
  • 10H. A. Gasteiger, S. S. Kocha, B. Sompalli, F. T. Wagner, Appl. Catal. B, 2005, 56, 9-35.

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