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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Cobalt and nickel selenide nanowalls anchored on graphene as bifunctional electrocatalysts for overall water splitting
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Cobalt and nickel selenide nanowalls anchored on graphene as bifunctional electrocatalysts for overall water splitting

机译:钴和硒化镍镍纳米壁锚固在石墨烯上作为双功能电催化剂,用于整体水分解

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摘要

The development of efficient and low-cost solar-driven overall water splitting systems for sustainable hydrogen generation is still a challenge. Herein, cobalt and nickel (Co and Ni) selenide nanowalls have been prepared on a conductive graphene coated Ni mesh substrate and used as electrocatalysts for hydrogen generation and oxygen evolution. The bifunctional CoSe nanowalls showed a high electrochemically active surface area, which manifested a low onset potential and high structural stability for overall water splitting. It afforded a 10 mA cm(-2) current density at -78 mV vs. RHE for the hydrogen evolution reaction and 150 mA cm(-2) at 1.74 V vs. RHE for the oxygen evolution reaction. No significant degradation was observed after a 24 h chronoamperometric test. A solar water electrolysis system was constructed by connecting the CoSe (+) and CoSe (-) pair with a photovoltaic cell in tandem, which showed a highest solar-to-hydrogen conversion efficiency of 6.65%. Its superior performance over industrial water electrolyzers provided a new possibility towards clean energy storage and utilization.
机译:高效,低成本的太阳能驱动的整体水分解系统的发展,以可持续地产生氢气仍然是一个挑战。在此,已经在涂覆有导电石墨烯的Ni网状基材上制备了钴和镍(Co和Ni)硒化物纳米壁,并将其用作产生氢和释放氧的电催化剂。双功能CoSe纳米壁显示出高的电化学活性表面积,这表明总水分解的起始电位低且结构稳定性高。对于氢气析出反应,它在-78 mV vs. RHE下提供了10 mA cm(-2)的电流密度,对于氧气析出反应,在1.74 V vs. RHE下提供了150 mA cm(-2)。 24小时计时电流测试后未观察到明显的降解。通过将CoSe(+)和CoSe(-)对与串联的光伏电池连接而构建了太阳能水电解系统,该系统显示出最高的6.65%的太阳能转化效率。它的性能优于工业水电解槽,为清洁能源的存储和利用提供了新的可能性。

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