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A Heterostructure Coupling of Exfoliated Ni-Fe Hydroxide Nanosheet and Defective Graphene as a Bifunctional Electrocatalyst for Overall Water Splitting

机译:剥落的镍铁氢氧化物纳米片和有缺陷的石墨烯作为双功能电催化剂的总结构水的异质结构耦合

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摘要

Herein, the authors demonstrate a heterostructured NiFe LDH-NS@DG10 hybrid catalyst by coupling of exfoliated Ni-Fe layered double hydroxide (LDH) nanosheet (NS) and defective graphene (DG). The catalyst has exhibited extremely high electrocatalytic activity for oxygen evolution reaction (OER) in an alkaline solution with an overpotential of 0.21 V at a current density of 10 mA cm(-2), which is comparable to the current record (approximate to 0.20 V in Fe-Co-Ni metal-oxide-film system) and superior to all other non-noble metal catalysts. Also, it possesses outstanding kinetics (Tafel slope of 52 mV dec(-1)) for the reaction. Interestingly, the NiFe LDH-NS@DG10 hybrid has also exhibited the high hydrogen evolution reaction (HER) performance in an alkaline solution (with an overpotential of 115 mV by 2 mg cm(-2) loading at a current density of 20 mA cm(-2)) in contrast to barely HER activity for NiFe LDH-NS itself. As a result, the bifunctional catalyst the authors developed can achieve a current density of 20 mA cm(-2) by a voltage of only 1.5 V, which is also a record for the overall water splitting. Density functional theory calculation reveals that the synergetic effects of highly exposed 3d transition metal atoms and carbon defects are essential for the bifunctional activity for OER and HER.
机译:在本文中,作者通过将剥落的Ni-Fe层状双氢氧化物(LDH)纳米片(NS)和有缺陷的石墨烯(DG)偶联,证明了一种异质结构的NiFe LDH-NS @ DG10杂化催化剂。在10 mA cm(-2)的电流密度下,该催化剂在过电位为0.21 V的碱性溶液中,对氧释放反应(OER)表现出极高的电催化活性,可与电流记录相媲美(约0.20 V在Fe-Co-Ni金属氧化物膜系统中),并且优于所有其他非贵金属催化剂。此外,它具有出色的动力学反应(Tafel斜率为52 mV dec(-1))。有趣的是,NiFe LDH-NS @ DG10杂化体还显示出在碱性溶液中的高氢气析出反应(HER)性能(在20 mA cm的电流密度下负载2 mg cm(-2)时产生115 mV的超电势) (-2))与NiFe LDH-NS本身几乎没有HER活性相反。结果,作者开发的双功能催化剂仅通过1.5 V的电压即可达到20 mA cm(-2)的电流密度,这也是整个水分解的记录。密度泛函理论计算表明,高度暴露的3d过渡金属原子和碳缺陷的协同效应对于OER和HER的双功能活性至关重要。

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  • 来源
    《Advanced Materials》 |2017年第17期|1700017.1-1700017.8|共8页
  • 作者单位

    Griffith Univ, Queensland Micro & Nanotechnol Ctr, Nathan, Qld 4111, Australia|Griffith Univ, Sch Nat Sci, Brisbane, Qld 4111, Australia;

    Griffith Univ, Queensland Micro & Nanotechnol Ctr, Nathan, Qld 4111, Australia|Griffith Univ, Sch Nat Sci, Brisbane, Qld 4111, Australia;

    Queensland Univ Technol, Sch Chem Phys & Mech Engn, Brisbane, Qld 4000, Australia;

    Shanghai Univ, Sch Environm & Chem Engn, 99 Shangda Rd, Shanghai 200444, Peoples R China;

    Griffith Univ, Environm Futures Res Inst, Brisbane, Qld 4111, Australia;

    Shanghai Univ, Sch Environm & Chem Engn, 99 Shangda Rd, Shanghai 200444, Peoples R China|Univ Queensland, Mat Engn, St Lucia, Qld 4072, Australia;

    Univ Queensland, Mat Engn, St Lucia, Qld 4072, Australia;

    Univ Queensland, Mat Engn, St Lucia, Qld 4072, Australia;

    Griffith Univ, Queensland Micro & Nanotechnol Ctr, Nathan, Qld 4111, Australia|Griffith Univ, Sch Nat Sci, Brisbane, Qld 4111, Australia;

    Shanghai Univ, Sch Environm & Chem Engn, 99 Shangda Rd, Shanghai 200444, Peoples R China;

    Univ Queensland, Mat Engn, St Lucia, Qld 4072, Australia;

    Queensland Univ Technol, Sch Chem Phys & Mech Engn, Brisbane, Qld 4000, Australia;

    Griffith Univ, Queensland Micro & Nanotechnol Ctr, Nathan, Qld 4111, Australia|Griffith Univ, Sch Nat Sci, Brisbane, Qld 4111, Australia;

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