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Atomically dispersed nickel–nitrogen–sulfur species anchored on porous carbon nanosheets for efficient water oxidation

机译:原子分散的镍-氮-硫物种固定在多孔碳纳米片上可实现有效的水氧化

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摘要

Developing low-cost electrocatalysts to replace precious Ir-based materials is key for oxygen evolution reaction (OER). Here, we report atomically dispersed nickel coordinated with nitrogen and sulfur species in porous carbon nanosheets as an electrocatalyst exhibiting excellent activity and durability for OER with a low overpotential of 1.51 V at 10 mA cm−2 and a small Tafel slope of 45 mV dec−1 in alkaline media. Such electrocatalyst represents the best among all reported transition metal- and/or heteroatom-doped carbon electrocatalysts and is even superior to benchmark Ir/C. Theoretical and experimental results demonstrate that the well-dispersed molecular S|NiNx species act as active sites for catalyzing OER. The atomic structure of S|NiNx centers in the carbon matrix is clearly disclosed by aberration-corrected scanning transmission electron microscopy and synchrotron radiation X-ray absorption spectroscopy together with computational simulations. An integrated photoanode of nanocarbon on a Fe2O3 nanosheet array enables highly active solar-driven oxygen production.
机译:开发低成本的电催化剂来代替贵重的基于Ir的材料是氧释放反应(OER)的关键。在这里,我们报道了多孔碳纳米片中与氮和硫物种配位的原子分散镍作为电催化剂,在10 mA excellentcm −2 下的低过电位1.51 V和较小的OER表现出优异的活性和耐久性。在碱性介质中的Tafel斜率为45 mV dec -1 。在所有报道的过渡金属和/或杂原子掺杂的碳电催化剂中,这种电催化剂表现最佳,甚至优于基准Ir / C。理论和实验结果表明,分散良好的S | NiNx分子可作为催化OER的活性中心。通过像差校正扫描透射电子显微镜和同步辐射X射线吸收光谱法以及计算模拟,清楚地揭示了碳基体中S | NiNx中心的原子结构。 Fe2O3纳米片阵列上集成的纳米碳光电阳极可实现高活性太阳能驱动的氧气生产。

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