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首页> 外文期刊>Nanoscale >Promoting photocatalytic hydrogen evolution over the perovskite oxide Pr-0.5(Ba0.5Sr0.5)(0.5)Co(0.8)Fe(0.2)O(3)by plasmon-induced hot electron injection
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Promoting photocatalytic hydrogen evolution over the perovskite oxide Pr-0.5(Ba0.5Sr0.5)(0.5)Co(0.8)Fe(0.2)O(3)by plasmon-induced hot electron injection

机译:促进光催化氢进化钙钛矿氧化物公关- 0.5 (Ba0.5Sr0.5)(0.5)(0.8)铁(0.2)O (3)plasmon-induced热电子注入

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摘要

Exploration of highly efficient and stable photocatalysts for water splitting has attracted much attention. However, developing a facile and effective approach to enhance the photocatalytic activity for practical applications is still highly challenging. Herein, we report a newly-fabricated perovskite oxide (Pr-0.5(Ba0.5Sr0.5)(0.5)Co0.8Fe0.2O3) decorated with Au ultrafine nanoparticles for photocatalytic water splitting. An exceptionally high hydrogen evolution rate of 1618 mu mol g(-1)h(-1)was achieved (under 2 h illumination) when the Au mass loading was optimized to 9.3 wt%, which is 540 times higher than that of the pristine one. The splendid photocatalytic activity of the sample was attributed to plasmon-excited hot electron injection from Au to Pr-0.5(Ba0.5Sr0.5)(0.5)Co0.8Fe0.2O3(PBSCF) under illumination. The finite-difference time-domain simulations (FDTD) demonstrated that the localized strong electric field formed at the interface between Au and PBSCF under illumination, enables the hot electrons to be energetic and make the injection possible.
机译:探索高效和稳定催化剂对水分裂吸引了太多的关注。有效的方法来提高光催化为实际应用程序仍然是活动的非常具有挑战性的。newly-fabricated钙钛矿氧化物(pr - 0.5 (Ba0.5Sr0.5) (0.5) Co0.8Fe0.2O3)装饰与非盟超细纳米颗粒光催化水分解。高氢进化率1618亩摩尔实现h g (1) (1) (2 h照明)9.3当非盟质量负载进行优化wt %,比高出540倍原始的。活动的示例是归因于plasmon-excited热电子注入从盟公关- 0.5 (Ba0.5Sr0.5) (0.5) Co0.8Fe0.2O3 (PBSCF)照明。模拟(FDTD)证明了局部强电场形成的盟和PBSCF之间的接口电子照明,使热精力充沛,使注入成为可能。

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