Aygün Mehtap, Guillen-Soler Melanie, Vila-Fungueiriño Jose M, Kurtoglu Abdullah, Chamberlain Thomas W, Khlobystov Andrei N, Del Carmen Gimenez-Lopez Maria
Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CIQUS), Universidade de Santiago de Compostela, 15782, Santiago de Compostela, Spain.
Present address: Faculty of Science, Erzurum Technical University, Erzurum, 25050, Turkey.
ChemSusChem. 2021 Nov 19;14(22):4973-4984. doi: 10.1002/cssc.202101236. Epub 2021 Sep 15.
Catalysts typically lose effectiveness during operation, with much effort invested in stabilising active metal centres to prolong their functional lifetime for as long as possible. In this study palladium nanoparticles (PdNP) supported inside hollow graphitised carbon nanofibers (GNF), designated as PdNP@GNF, opposed this trend. PdNP@GNF exhibited continuously increasing activity over 30000 reaction cycles when used as an electrocatalyst in the hydrogen evolution reaction (HER). The activity of PdNP@GNF, expressed as the exchange current density, was always higher than activated carbon (Pd/C), and after 10000 cycles PdNP@GNF surpassed the activity of platinum on carbon (Pt/C). The extraordinary durability and self-improving behaviour of PdNP@GNF was solely related the unique nature of the location of the palladium nanoparticles, that is, at the graphitic step-edges within the GNF. Transmission electron microscopy imaging combined with spectroscopic analysis revealed an orchestrated series of reactions occurring at the graphitic step-edges during electrocatalytic cycling, in which some of the curved graphitic surfaces opened up to form a stack of graphene layers bonding directly with Pd atoms through Pd-C bonds. This resulted in the active metal centres becoming effectively hardwired into the electrically conducting nanoreactors (GNF), enabling facile charge transport to/from the catalytic centres resulting in the dramatic self-improving characteristics of the electrocatalyst.
催化剂在运行过程中通常会失去活性,人们投入了大量精力来稳定活性金属中心,以尽可能延长其功能寿命。在本研究中,负载在中空石墨化碳纳米纤维(GNF)内部的钯纳米颗粒(PdNP),即PdNP@GNF,却与这一趋势相反。当用作析氢反应(HER)的电催化剂时,PdNP@GNF在30000个反应循环中表现出活性持续增加。以交换电流密度表示的PdNP@GNF的活性始终高于活性炭(Pd/C),并且在10000个循环后,PdNP@GNF超过了碳载铂(Pt/C)的活性。PdNP@GNF非凡的耐久性和自我提升行为完全与钯纳米颗粒的独特位置性质有关,即位于GNF内的石墨台阶边缘处。透射电子显微镜成像结合光谱分析揭示了在电催化循环过程中,在石墨台阶边缘发生了一系列精心编排的反应,其中一些弯曲的石墨表面打开形成了一层石墨烯层,通过Pd-C键与Pd原子直接结合。这导致活性金属中心有效地硬连接到导电纳米反应器(GNF)中,使得电荷能够轻松地进出催化中心,从而产生了电催化剂显著的自我提升特性。