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首页> 外文期刊>Applied Surface Science >Co_(1.4)Ni_(0.6)P cocatalysts modified metallic carbon black/g-C_3N_4 nanosheet Schottky heterojunctions for active and durable photocatalytic H_2 production
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Co_(1.4)Ni_(0.6)P cocatalysts modified metallic carbon black/g-C_3N_4 nanosheet Schottky heterojunctions for active and durable photocatalytic H_2 production

机译:Co_(1.4)Ni_(0.6)P助催化剂改性的金属炭黑/ g-C_3N_4纳米片肖特基异质结,用于活性和持久性光催化H_2的生产

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摘要

Efficient separation and utilization of photogenerated electrons as well as holes play decisive roles in boosting photocatalytic hydrogen evolution reaction (HER). To reach this goal, we designed carbon black (CB) and Co1.4Ni0.6P as dual cocatalysts co-modified graphitic carbon nitride for efficient and stable photocatalytic HER. This resulting ternary photocatalyst was synthesized by sonochemical loading and high-temperature phosphatizing. Impressively, the maximum photocatalytic hydrogen-production rate for the ternary photocatalysts could reach 405 mu molh(-1) g(-1) , which was 810,2 and 1.7 times higher than those of pure g-C3N4 (0.5 mu molh(-1) g(-1)), g-C3N4-Co1.4Ni0.6P (195 mu molh(-1)g(-1)) and g-C3N4-1% Pt (230 mu molh(-1)g(-1)), respectively. Through the test analysis, the enhanced hydrogen-evolution performance was attributed to the synergetic effect between the metallic CB and the low-cost Co1.4Ni0.6P cocatalyst. More interestingly, the Co1.4Ni0.6P cocatalyst could not only decrease the recombination of photogenerated electrons and holes, but also boost absorption in the visible region and the hydrogen-evolution kinetics. Furthermore, the formation of Schottky heterojunctions between metallic CB and g-C3N4 nanosheets could further accelerate the separation and transfer of photogenerated electrons. This work provides a simple and facile strategy to rationally design highly efficient photocatalyst using low-cost nano-carbon materials and high-activity metal phosphide.
机译:光生电子的有效分离和利用以及空穴在促进光催化氢释放反应(HER)中起着决定性的作用。为了实现此目标,我们设计了炭黑(CB)和Co1.4Ni0.6P作为双重助催化剂,共改性的石墨氮化碳,以实现高效,稳定的光催化HER。通过声化学负载和高温磷酸化来合成这种三元光催化剂。令人印象深刻的是,三元光催化剂的最大光催化产氢率可达到405μmolh(-1)g(-1),比纯g-C3N4(0.5μmolh(- 1)g(-1)),g-C3N4-Co1.4Ni0.6P(195摩尔(-1)g(-1))和g-C3N4-1%Pt(230摩尔(-1)g( -1))。通过测试分析,氢释放性能的提高归因于金属CB与低成本Co1.4Ni0.6P助催化剂之间的协同作用。更有趣的是,Co1.4Ni0.6P助催化剂不仅可以减少光生电子和空穴的复合,而且可以提高可见光区域的吸收和氢演化动力学。此外,在金属CB和g-C3N4纳米片之间形成肖特基异质结可以进一步加速光生电子的分离和转移。这项工作提供了一种简单而又简便的策略,可以使用低成本的纳米碳材料和高活性金属磷化物合理设计高效的光催化剂。

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