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Edge-dominated hydrogen evolution reactions in ultra-narrow MoS<inf>2</inf> nanoribbon arrays

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F23%3A00573967" target="_blank" >RIV/61388955:_____/23:00573967 - isvavai.cz</a>

  • Result on the web

    <a href="https://hdl.handle.net/11104/0344350" target="_blank" >https://hdl.handle.net/11104/0344350</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d3ta01573d" target="_blank" >10.1039/d3ta01573d</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Edge-dominated hydrogen evolution reactions in ultra-narrow MoS<inf>2</inf> nanoribbon arrays

  • Original language description

    Future energy generation and storage requirements emphasize the importance of high-performance electrocatalysis. MoS2 edges exhibit ideal energetics for hydrogen evolution reactions (HERs) if challenges in their kinetics are addressed. Herein, we investigate the emergence of edge-dominated electrochemical reaction kinetics in ultra-narrow MoS2 nanoribbons. A templated subtractive patterning process (TSPP) served as a powerful platform that yields large arrays of MoS2 nanoribbons. Nanoribbons with widths below 30 nm exhibit significantly increased reaction kinetics, as evidenced by a ∼200-fold enhanced turn-over frequency, an 18-fold increased exchange current density, and a 38% decreased Tafel slope. These improvements are due to increased charge transfer efficiency from the basal plane toward the edge sites. Photo-electrocatalytic measurements and carrier transport simulations reveal the impact of suppressed band bending in nanoribbons below the depletion width toward achieving edge-dominated HER. Our results demonstrate the potential of confinement in electrocatalysis and provide a universal route toward nanoribbon-enhanced electrochemistry.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    <a href="/en/project/GX20-08633X" target="_blank" >GX20-08633X: ÅrchitectRonics of Two-dimensional crystals via synergy of chiral electro-chemical and opto-electronic concepts on Å-scale</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Materials Chemistry A

  • ISSN

    2050-7488

  • e-ISSN

    2050-7496

  • Volume of the periodical

    11

  • Issue of the periodical within the volume

    29

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    15802-15810

  • UT code for WoS article

    001019860100001

  • EID of the result in the Scopus database

    2-s2.0-85165261468