State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, P.O. Box 98, Beijing, 100029, P. R. China.
Small. 2016 May;12(18):2492-8. doi: 10.1002/smll.201600189. Epub 2016 Mar 21.
Catalysts screening and structural optimization are both essential for pursuing a high-efficient water electrolysis system (WES) with reduced energy supply. This study demonstrates an advanced WES with double superaerophobic electrodes, which are achieved by constructing a nanostructured NiMo alloy and NiFe layered double hydroxide (NiFe-LDH) films for hydrogen evolution and oxygen evolution reactions, respectively. The superaerophobic property gives rise to significantly reduced adhesion forces to gas bubbles and thereby accelerates the hydrogen and oxygen bubble releasing behaviors. Benefited from these metrics and the high intrinsic activities of catalysts, this WES affords an early onset potential (≈1.5 V) for water splitting and ultrafast catalytic current density increase (≈0.83 mA mV(-1) ), resulting in ≈2.69 times higher performance compared to the commercial Pt/C and IrO2 /C catalysts based counterpart under 1.9 V. Moreover, enhanced performance at high temperature as well as prominent stability further demonstrate the practical application of this WES.
催化剂的筛选和结构优化对于追求高效的水电解系统(WES)以减少能源供应都是至关重要的。本研究展示了一种具有双超疏水性电极的先进的 WES,该电极通过分别构建纳米结构的 NiMo 合金和 NiFe 层状双氢氧化物(NiFe-LDH)薄膜来实现析氢和析氧反应。超疏水性导致气体气泡的附着力显著降低,从而加速了氢气和氧气气泡的释放行为。受益于这些指标和催化剂的高内在活性,该 WES 在水分解时提供了较早的起始电位(≈1.5 V)和超快的催化电流密度增加(≈0.83 mA mV(-1)),与基于商业 Pt/C 和 IrO2 /C 催化剂的对应物相比,在 1.9 V 下的性能提高了约 2.69 倍。此外,在高温下的性能增强以及突出的稳定性进一步证明了该 WES 的实际应用。