Exploiting tripeptide in Pd/C for boosting hydrogen production from formic acid dehydrogenation†

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Science & Technology Pub Date : 2024-12-02 DOI:10.1039/D4CY01111B
Yan Gu, Hongli Wang, Yaohao Zhang, Lu Yang, Xiaoshan Liu and Xuesong Li
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Abstract

Designing highly efficient catalysts for driving the hydrogen production from formic acid (FA) dehydrogenation is of considerable practical importance for future hydrogen economies. Herein, ultrafine Pd nanoparticles (NPs) with lattice strain induced by the incorporation of tripeptide (TPT) anchored on commercial Vulcan XC-72R carbon (Pd/C-TPT) are fabricated by a facile wet-chemical process. Remarkably, the obtained Pd/C-TPT catalyst presents an extraordinary catalytic activity towards dehydrogenation of FA without any additives, giving an initial turnover frequency (TOF) value as high as 2102 mol H2 per mol Pd per h at 323 K, which is 8.4 times than that of the Pd/C catalyst, and even much higher than most of other superior Pd catalysts reported so far. The characterization results reveal that the strain effect and size effect caused by the strong interaction between the Pd NPs and TPT tune the electronic structure of Pd for optimized formate adsorption. This study provides more flexibility for a facile and controllable synthesis strategy of efficient catalysts toward FA dehydrogenation for hydrogen production.

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利用Pd/C中三肽促进甲酸脱氢产氢†
设计高效的甲酸脱氢制氢催化剂对未来氢经济具有重要的现实意义。本文采用湿法制备了由三肽(TPT)结合在商业Vulcan XC-72R碳(Pd/C-TPT)上引起晶格应变的超细Pd纳米颗粒(NPs)。值得注意的是,所制备的Pd/C- tpt催化剂在不添加任何添加剂的情况下,对FA脱氢表现出了非凡的催化活性,在323 K时,其初始周转频率(TOF)高达2102 mol H2 / mol Pd/ h,是Pd/C催化剂的8.4倍,甚至远高于目前报道的大多数优异Pd催化剂。表征结果表明,Pd NPs与TPT之间的强相互作用引起的应变效应和尺寸效应调节了Pd的电子结构,从而优化了对甲酸盐的吸附。该研究为FA脱氢制氢高效催化剂的合成策略提供了更大的灵活性和可控性。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
期刊最新文献
Inside back cover Back cover Back cover Enhancing activity and selectivity of palladium catalysts in ketone α-arylation by tailoring the imine chelate of pyridinium amidate (PYA) ligands. Reduction behavior of PdO-NiO/SiO2: how Pd location affects cinnamaldehyde hydrogenation.
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