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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >CdS/Au/Ti/Pb(Mg1/3Nb2/3)(0.7)Ti0.3O3 photocatalysts and biphotoelectrodes with ferroelectric polarization in single domain for efficient water splitting
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CdS/Au/Ti/Pb(Mg1/3Nb2/3)(0.7)Ti0.3O3 photocatalysts and biphotoelectrodes with ferroelectric polarization in single domain for efficient water splitting

机译:CDS / AU / TI / PB(MG1 / 3NB2 / 3)(0.7)Ti0.3O3光催化剂和具有单结构域铁电极化的光催化剂,用于高效的水分裂

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摘要

The construction of efficient photocatalysts for water splitting is still challenging, mainly due to the unexpected recombination of photogenerated carriers. Ferroelectric polarization-induced charge separation of photo catalysts has been demonstrated as an effective method for improving photocatalytic performance. However, ferroelectric domains in existing works are random before polarization-switching, which results in lower polarization electric field intensity and limits the charge separation efficiency. Here, we report that the spontaneous ferroelectric polarization in a single domain for efficient charge separation over a representative semiconductor CdS, in the form of CdS/Au/Ti/Pb(Mg1/3Nb2/3)(0.7)Ti0.3O3 (CdS/Au/Ti/PMN-PT), for water splitting in absence of any cocatalyst or external voltage. The photocurrent value of the positive polarized CdS/Au/Ti/PMN-PT yields 1.70 mA.cm(-2), which is about 20 times higher than the value of the non-polarized sample. In addition, a biphotoelectrode cell composed of a positively and a negatively polarized CdS/Au/Ti/PMN-PT was constructed. A considerable solar-to-hydrogen conversion efficiency of 0.19% was achieved. It was found that the interfacial resistance and the surface reaction kinetics may be the main factors governing the photocatalytic performance. This work not only provides a strategy to promote charge separation but also develops a new biphotoelectrode cell capable of obtaining efficient solar water splitting.
机译:用于水分分裂的高效光催化剂的构建仍然具有挑战性,主要是由于光发生载体的意外重组。已经证明了光电偏振诱导的光催化剂的电荷分离作为改善光催化性能的有效方法。然而,现有作品中的铁电域在偏振开关之前是随机的,这导致偏振电场强度较低并限制电荷分离效率。在这里,我们报告说,单个结构域中的自发铁电偏振以CDS / AU / Ti / Pb(Mg1 / 3nb2 / 3)(0.7)Ti0.3O3(CD / Au / ti / pmn-pt),用于在没有任何助催化剂或外部电压的情况下分裂。正极化CDS / Au / Ti / PMN-PT的光电流值为1.70 mA.CM(-2),比非极化样品的值高约20倍。另外,构建由正极和带负偏振CDS / AU / Ti / PMN-PT组成的双电极电池。实现了0.19%的相当大的太阳能转换效率。发现界面抗性和表面反应动力学可能是控制光催化性能的主要因素。这项工作不仅提供了促进电荷分离的策略,而且还开发了能够获得高效的太阳能分裂的新的双光电电极。

著录项

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  • 作者单位

    Univ Sci &

    Technol China Collaborat Innovat Ctr Chem Energy Mat Natl Synchrotron Radiat Lab Hefei 230029 Anhui Peoples R China;

    Univ Sci &

    Technol China Collaborat Innovat Ctr Chem Energy Mat Natl Synchrotron Radiat Lab Hefei 230029 Anhui Peoples R China;

    Univ Sci &

    Technol China Collaborat Innovat Ctr Chem Energy Mat Natl Synchrotron Radiat Lab Hefei 230029 Anhui Peoples R China;

    Univ Sci &

    Technol China Collaborat Innovat Ctr Chem Energy Mat Natl Synchrotron Radiat Lab Hefei 230029 Anhui Peoples R China;

    Anhui Univ Sch Chem &

    Chem Engn Hefei 230601 Anhui Peoples R China;

    Chinese Acad Sci Inst Appl Technol Hefei Inst Phys Sci Hefei 230031 Anhui Peoples R China;

    Chinese Acad Sci Beijing Adv Sci &

    Innovat Ctr Beijing 100083 Peoples R China;

    Univ Sci &

    Technol China Collaborat Innovat Ctr Chem Energy Mat Natl Synchrotron Radiat Lab Hefei 230029 Anhui Peoples R China;

    Univ Sci &

    Technol China Collaborat Innovat Ctr Chem Energy Mat Natl Synchrotron Radiat Lab Hefei 230029 Anhui Peoples R China;

    Univ Sci &

    Technol China Collaborat Innovat Ctr Chem Energy Mat Natl Synchrotron Radiat Lab Hefei 230029 Anhui Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 催化;
  • 关键词

    Photocatalysis; Ferroelectric polarization; CdS; Water splitting; Pb(Mg1/3Nb2/3)(0.7)Ti0.3O3;

    机译:光催化;铁电偏振;CD;水分裂;Pb(Mg1 / 3nb2 / 3)(0.7)Ti0.3O3;

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