Nanoarchitectured N-Heterocyclic Carbene-Pt Nanoparticles on Carbon Nanotubes: Toward Advanced Electrocatalysis in the Hydrogen Evolution Reaction

被引:1
作者
Rapakousiou, Amalia [1 ]
Minadakis, Michail P. [1 ]
Chalkidis, Savvas G. [2 ]
Ruiz-Gonzalez, Maria Luisa [3 ]
Navio, Cristina [4 ]
Vougioukalakis, Georgios C. [2 ]
Tagmatarchis, Nikos [1 ]
机构
[1] Natl Hellen Res Fdn, Theoret & Phys Chem Inst, Athens 11635, Greece
[2] Natl & Kapodistrian Univ Athens, Dept Chem, Lab Organ Chem, Athens 15771, Greece
[3] Univ Complutense Madrid, Dept Quim Inorgan, Madrid 28040, Spain
[4] IMDEA Nanosci, C Faraday 9,Ciudad Univ Cantoblanco, Madrid 28049, Spain
关键词
hydrogen evolution reaction (HER); electrocatalysis; platinum nanoparticles (PtNPs); N-heterocyclic carbenes(NHCs); carbon nanotubes; redox behavior; specific activity; mass activity; PLATINUM NANOPARTICLES; PERFORMANCE; CATALYSTS; SURFACE; FUNCTIONALIZATION; GRAPHENE;
D O I
10.1021/acsami.5c02182
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In response to the need for sustainable energy, this study focuses on advancing the electrocatalytic Hydrogen Evolution Reaction (HER). Considering platinum-based catalysts' efficacy, but acknowledging their cost and scarcity implications, our work pursues Pt content minimization, simultaneously upholding catalytic efficiency. Our approach introduces a precisely engineered nanoarchitecture, leveraging multiwalled carbon nanotubes (MWCNTs) bearing anchored N-heterocyclic carbenes (NHCs). These carbenes form robust covalent bonds with ultrastable, highly crystalline, platinum nanoparticles (PtNPs), establishing MWCNTs-NHC-PtNPs as a highly efficient electrocatalyst. The synergistic effect of NHCs and triazole moieties facilitates controlled nanoparticle growth and stabilization, yielding 2.0 +/- 0.3 nm, uniformly distributed {1 1 1}-faceted PtNPs. The as-obtained MWCNTs-NHC-PtNPs nanomaterial exhibits exceptional HER efficiency in 0.5 M H2SO4 with an overpotential of 77 mV at -10 mA cm-2 and a 50 mV dec-1 Tafel slope, despite containing a merely 0.4% Pt/C atomic ratio content, as determined by XPS. Notably, at 200 mV overpotential, the mass activity reaches 8.6 A/mgPt and the specific activity is 53 mA/cm2 Pt, highlighting the efficiency of each Pt site within this nanostructure. Cyclic voltammetry reveals a distinctive, reversible PtO/Pt redox process, demonstrating surface-controlled and diffusion-assisted kinetics with charge storage properties that stabilize the electrocatalyst's electron-surface and facilitate proton reduction. Equally important, the nanoarchitecture prevents aggregation and mitigates Pt irreversible oxidation, showcasing enhanced stability after extensive cycling and exposure to air. Comparative analyses with a control electrocatalyst lacking NHC-PtNPs ligation emphasize the unique role of NHC-Pt (0) bonding in enhancing electrocatalytic efficiency. Comprehensive surface and electronic property analyses validate the potential of the MWCNTs-NHC-PtNPs platform.
引用
收藏
页码:28138 / 28150
页数:13
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