首页> 外文期刊>Catalysis science & technology >Hierarchical dandelion-flower-like cobalt-phosphide modified CdS/reduced graphene oxide-MoS2 nanocomposites as a noble-metal-free catalyst for efficient hydrogen evolution from water
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Hierarchical dandelion-flower-like cobalt-phosphide modified CdS/reduced graphene oxide-MoS2 nanocomposites as a noble-metal-free catalyst for efficient hydrogen evolution from water

机译:分层dandelion-flower-likecobalt-phosphide修改cd /降低石墨烯作为一个noble-metal-free oxide-MoS2纳米复合材料高效的催化剂氢进化水

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摘要

Commercial applications of sustainable photocatalytic hydrogen production via water-splitting, an important future source of renewable energy, are hindered by the high price and scarcity of the requisite noble metal co-catalysts. This problem could be overcome by developing highly active and durable noble-metalfree photocatalysts. Herein, a new solar-light-active noble-metal-free catalyst featuring dandelion-flower-like cobalt-phosphide embedded with CdS nanostructures grown on reduced graphene oxide (RGO)-MoS2 nanosheets was designed, and its photocatalytic hydrogen production activity was evaluated in water under simulated sunlight irradiation using lactic acid as a sacrificial reagent. The results show that the optimized CdS/RGO-MoS2@CoP photocatalyst exhibited an efficient H-2 production rate of 83907 mu mol h(-1) g(-1) with an apparent quantum efficiency of 22.5%, far exceeding those of bare CdS (1053 mu mol h(-1) g(-1)), CdS-RGO (12 177 mu mol h(-1) g(-1)), CdS-RGO-MoS2 (29 268 mu mol h(-1) g(-1)), CdS: CoP (32 606 mu mol h(-1) g(-1)), CdS/CoP-RGO (54 259 mu mol h(-1) g(-1)) and CdS:Pt (12 478 mu mol h(-1) g(-1)) nanostructures. The proposed mechanism for the enhancement of the photocatalytic hydrogen evaluation rate of CdS/MoS2-RGO@CoP is based on the efficient separation of photogenerated electron-hole pairs. In the nanocomposite, the wrapped RGO nanosheets serve as good electron collectors and transporters. Meanwhile, the MoS2 and CoP nanostructures serve as a co-catalyst and electron acceptor, respectively, for the effective separation of the photo-charge carrier from the bare nanostructures, thereby decreasing the probability of electron-hole recombination at the interface of the nanocomposites and further stimulating the surface H-2-evolution kinetics. We believe that this work provides invaluable information for the design of new, efficient sunlight-active noble-metalfree photocatalysts for hydrogen production through water-splitting.
机译:商业应用的可持续通过光催化制氢水分解,将来的一个重要来源可再生能源,受到多重阻碍高昂的代价和缺乏必要的贵金属co-catalysts。开发高活性和耐用noble-metalfree催化剂。solar-light-active noble-metal-free催化剂以dandelion-flower-like cobalt-phosphide内置cd纳米结构生长在减少石墨烯氧化物(RGO)二硫化钼nanosheets设计,其光催化氢生产活动是评估在水中使用乳酸模拟阳光照射作为牺牲试剂。优化的cd / RGO-MoS2@CoP光催化剂表现出一种有效的2生产的速度83907亩摩尔h (1) g(1)具有明显的量子效率为22.5%,远远超过那些光秃秃的cd(1053亩摩尔h (1) g (1)), CdS-RGO(12 177亩摩尔h (1) g (1)), CdS-RGO-MoS2(29 268亩摩尔h (1) g (1)), cd:警察(32 606亩摩尔h (1)g(1))、cd / CoP-RGO(54 259亩摩尔h (1) g (1))和cd: Pt(12 478亩摩尔h (1) g (1))纳米结构。提高光催化的氢评价的cd / MoS2-RGO@CoP是基于photogenerated的有效分离电子空穴对。包装RGO nanosheets作为良好的电子收藏家和转运蛋白。和警察纳米结构作为co-catalyst和电子受体,分别photo-charge载体的有效分离从光秃秃的纳米结构,从而减少电子空穴复合的概率纳米复合材料,进一步的接口刺激表面H-2-evolution动力学。我们相信这项工作提供了宝贵的信息设计新的高效sunlight-active noble-metalfree催化剂通过水分解制氢。

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