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Engineering an Earth-Abundant Element-Based Bifunctional Electrocatalyst for Highly Efficient and Durable Overall Water Splitting

机译:设计一种基于地球元素的双功能电催化剂,以实现高效,持久的总水分解

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摘要

The simultaneous and efficient evolution of hydrogen and oxygen with earth-abundant, highly active, and robust bifunctional electrocatalysts is a significant concern in water splitting. Herein, non-noble metal-based Ni-Co-S bifunctional catalysts with tunable stoichiometry and morphology are realized. The engineering of electronic structure and subsequent morphological design synergistically contributes to significantly elevated electrocatalytic performance. Stable overpotentials (eta(10)) of 243 mV (vs reversible hydrogen electrode) for oxygen evolution reaction (OER) and 80 mV for hydrogen evolution reaction (HER), as well as Tafel slopes of 54.9 mV dec(-1) for OER and 58.5 mV dec(-1) for HER, are demonstrated. In addition, density functional theory calculations are performed to determine the optimal electronic structure via the electron density differences to verify the enhanced OER activity is related to the Co top site on the (110) surface. Moreover, the tandem bifunctional NiCo2S4 exhibit a required voltage of 1.58 V (J = 10 mA cm(-2)) for simultaneous OER and HER, and no obvious performance decay is observed after 72 h. When integrated with a GaAs solar cell, the resulting photoassisted water splitting electrolyzer shows a certified solar-to-hydrogen efficiency of up to 18.01%, further demonstrating the feasibility of engineering protocols and the promising potential of bifunctional NiCo2S4 for large-scale overall water splitting.
机译:氢和氧与富含地球,高活性和坚固的双功能电催化剂的同时高效释放是水分解中的重要问题。在此,实现了具有可调整的化学计量和形态的非贵金属基Ni-Co-S双功能催化剂。电子结构的工程设计和随后的形态设计协同作用,有助于显着提高电催化性能。氧释放反应(OER)的稳定过电位(eta(10))为243 mV(相对可逆氢电极),氢释放反应的稳定过电位(eta(10))为80 mV(HER),OER的Tafel斜率为54.9 mV dec(-1)并证明了HER的58.5 mV dec(-1)。另外,执行密度泛函理论计算以通过电子密度差确定最佳电子结构,以验证增强的OER活性与(110)表面上的Co顶部位点有关。此外,串联双功能NiCo2S4展示了同时进行OER和HER所需的1.58 V(J = 10 mA cm(-2))电压,并且在72 h后未观察到明显的性能下降。当与GaAs太阳能电池集成时,所得的光辅助水分解电解槽显示出经认证的高达18.01%的太阳能转化效率,这进一步证明了工程方案的可行性以及双功能NiCo2S4在大规模整体水分解中的潜力。

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  • 来源
    《Advanced Functional Materials》 |2019年第9期|1807031.1-1807031.10|共10页
  • 作者单位

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Civil & Environm Engn Sch, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Sch Mat Sci & Engn, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China|Univ Sci & Technol Beijing, Beijing Municipal Key Lab New Energy Mat & Techno, Beijing 100083, Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
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  • 关键词

    bifunctional electrocatalysts; earth-abundant elements; electronic structure engineering; morphology engineering overall water splitting;

    机译:双功能电催化剂;稀土元素;电子结构工程;形态工程整体水分解;

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