Pt/MoC的制备及其在电解水析氢反应中的催化性能
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  • 英文篇名:Preparation of Pt/MoC and Its Performance in Electrolysis Hydrogen Evolution
  • 作者:周燕强 ; 陈萌 ; 徐立军 ; Abuliti ; Abudula ; 马宇飞 ; 方岩雄
  • 英文作者:ZHOU Yan-qiang;CHEN Meng;XU Li-jun;Abuliti Abudula;MA Yu-fei;FANG Yan-xiong;School of Light Industry and Chemical Engineering, Guangdong University of Technology;Xinjiang Institute of Engineering;
  • 关键词:再生能源 ; 催化剂 ; 电解水 ; 制氢 ; 有机电化学与工业
  • 英文关键词:renewable energy;;catalyst;;electrolyzed water;;hydrogen production;;electro-organic chemistry and industry
  • 中文刊名:JXHG
  • 英文刊名:Fine Chemicals
  • 机构:广东工业大学轻工化工学院;新疆工程学院;
  • 出版日期:2018-04-12 11:07
  • 出版单位:精细化工
  • 年:2018
  • 期:v.35
  • 基金:国家自然科学基金(21776049);国家自然科学基金青年科学基金(51701046)~~
  • 语种:中文;
  • 页:JXHG201811018
  • 页数:7
  • CN:11
  • ISSN:21-1203/TQ
  • 分类号:126-132
摘要
以钼酸铵和氯铂酸为原料,通过原位程序升温碳化过程,合成了Pt负载量不同的Pt/MoxCy(x∶y≤2)催化剂,并考察了其在电解水析氢反应(HER)中的催化性能。利用XRD、BET、SEM、TEM、XPS对催化剂的微观结构及物理化学性质进行了表征。结果表明,Pt的负载改变了碳化钼形成的拓扑结构,Pt负载后的样品更容易形成α-Mo_2C相。Pt的负载量对碳化钼催化剂在HER反应中的催化性能具有显著影响,1.6Pt/MoC[n(Pt)∶n(Mo)=1.6∶98.4]催化剂表现出最优催化效果(过电势ηonset=108m V,塔菲尔斜率b=74m V/dec)及较低的阻抗(18.77?),可以与商业Pt/C催化剂相媲美。
        Pt/Mo_xC_y(x∶y≤2) catalysts with different Pt loadings were synthesized using ammonium molybdate and chloroplatinic acid as raw materials through in situ temperature-programmed carbonization process and their catalytic activities in the hydrogen evolution reaction(HER) of electrolyzed water were investigated. Their microstructure and physicochemical properties were characterized by XRD, BET, SEM, TEM and XPS. The results showed that the introduction of Pt changed the topological structure of molybdenum carbide during the carbonization process and made the prepared samples easier to form the α-Mo_2C phase. The loading of Pt had a significant effect on the catalytic activity of molybdenum carbide catalyst in the HER reaction. Among the samples, the 1.6 Pt/MoC [n(Pt) ∶n(Mo)=1.6∶98.4]catalyst exhibited the best catalytic activity(overpotential ηonset=108 mV, Tafel slope b=74 mV/dec) and had lower impedance(18.77 ?), which could be comparable with the commercial Pt/C catalyst.
引文
[1]Steele B C,Heinzel A.Materials for fuel-cell technologies[J].Nature,2001,414(6861):345-352.
    [2]Kreuter W,Hofmannz H.The important energy transformer in a world of sustainable energy[J].International Journal of Hydrogen Energy,1996,23(8):661-666.
    [3]Debe M K.Electrocatalyst approaches and challenges for automotive fuel cells[J].Nature,2012,486(7401):43-51.
    [4]Walter M G,Warren E L,McKone J R,et al.Solar water splitting cells[J].Chemical Reviews,2010,110(11):6446-6473.
    [5]Bartak D E,Kazee B,Shimazu K,et al.Electrodeposition and characterization of platinum microparticles in poly(4-vinylpyridine)film electrodes[J].Analytical Chemistry,1986,58(13):2756-2761.
    [6]Millet P,Andolfatto F,Durand R.Design and performance of a solid polymer electrolyte water electrolyzer[J].International Journal of Hydrogen Energy,1996,21(2):87-93.
    [7]Levy R B,Boudan M.Platinum-like behavior of tungsten carbide in surface catalysis[J].Science,1973,181(4099):547-549.
    [8]de Novion C H,Landesman J P.Order and disorder in transition metal carbides and nitrides:experimental and theoretical aspects[J].Pure and Applied Chemistry,1985,57(10):1391-1402.
    [9]Vrubel H,Hu Xile.Molybdenum boride and carbide catalyze hydrogen evolution in both acidic and basic solutions[J].Angewandte Chemie-International Edition,2012,51(51):12703-12706.
    [10]Ma Y F,Guan G Q,Hao X G,et al.Molybdenum carbide as alternative catalyst for hydrogen production-A review[J].Renewable and Sustainable Energy Reviews,2017,75:1101-1129.
    [11]Bouchy C,Schmidt I,Anderson J,et al.Metastable fccα-MoC1-x supported on HZSM5:preparation and catalytic performance for the non-oxidativeconversion of methane to aromatic compounds[J].Journal of Molecular Catalysis A Chemical,2000,163(1):283-296.
    [12]Ranhotra G,Bell A,Reimer J.Catalysis over molybdenum carbides and nitrides:Ⅱ.Studies of CO hydrogenation and C2H6hydrogenolysis[J].Journal of Catalysis,1987,108(1):40-49.
    [13]Ma Y F,Guan G Q,Shi C,et al.Low-temperature steam reforming of methanol to produce hydrogen over various metal-doped molybdenum carbide catalysts[J].International Journal of Hydrogen Energy,2014,39(1):258-266.
    [14]Jung K T,Kim W B,Rhee C H,et al.Effects of transition metal addition on the solidstate transformation of molybdenum trioxide to molybdenum carbides[J].Chemistry of Materials,2004,16(2):307-314.
    [15]Shi C,Zhang A J,Li X S,et al.Ni-modified Mo2C catalysts for methane dry reforming[J].Applied Catalysis A:General,2012,431(29):164-170.
    [16]Vilekar S A,Fishtik I,Datta R.Kinetics of the hydrogen electrode reaction[J].Journal of the Electrochemical Society,2010,157(7):1040-1050.
    [17]Lin H,Liu N,Shi Z,et al.Cobalt-doping in molybdenum-carbide nanowires toward efficient electrocatalytic hydrogen evolution[J].Advanced Functional Materials,2016,26(31):5590-5598.
    [18]Oki S,Mezalki R.Identification of rate-controlling steps for the water-gas shift reaction over an iron oxide catalyst[J].The Journal of Physical Chemistry,1973,77(4):447-452.

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