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Enhanced Hydrogen Evolution Reaction Catalysis at Template-Free Liquid/Liquid Interfaces by in Situ Electrodeposited Amorphous Molybdenum Sulfide on Carbon Nanotubes

ACS Applied Energy Materials · Ağustos 2021

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YÖKSİS Kayıtları
Enhanced Hydrogen Evolution Reaction Catalysis at Template-Free Liquid/Liquid Interfaces by In Situ Electrodeposited Amorphous Molybdenum Sulfide on Carbon Nanotubes
ACS Applied Energy Materials · 2021 SCI-Expanded
Prof. Dr. İMREN HATAY PATIR →
Enhanced Hydrogen Evolution Reaction Catalysis at Template-Free Liquid/Liquid Interfaces by In Situ Electrodeposited Amorphous Molybdenum Sulfide on Carbon Nanotubes
ACS Applied Energy Materials · 2021 SCI-Expanded
Dr. Öğr. Üyesi GİZEM YILDIZ →
Enhanced Hydrogen Evolution Reaction Catalysis at Template-Free Liquid/Liquid Interfaces by In Situ Electrodeposited Amorphous Molybdenum Sulfide on Carbon Nanotubes
ACS Applied Energy Materials · 2021 SCI-Expanded
Doç. Dr. EMRE ASLAN →

Makale Bilgileri

Dergi ACS Applied Energy Materials
Yayın TarihiAğustos 2021
Cilt / Sayfa4 · 8330-8339
Özet In situ deposited catalysts are drawing great attention in the hydrogen evolution reaction for photocatalytic and electrocatalytic processes due to their inexpensive and simple preparation methods. Molybdenum sulfide derivatives are convenient alternatives to the well-known and efficient noble metallic catalyst Pt due to their uncostly and abundant nature. Herein, liquid/liquid interfaces are chosen to determine the catalytic activity of a template-free nanocomposite catalyst composed of MoSx grown in situ on multiwalled CNTs (CNT/MoSx) during catalytic hydrogen production for the first time. The organic sacrificial agent decamethylferrocene plays the role of a reductant for both (NH4)2MoS4 and protons to obtain MoSx and molecular hydrogen, respectively. The catalytic activity of CNT/MoSx is investigated by four-electrode voltammetry and biphasic reactions at the water/1,2-dichloroethane (DCE) interface. In addition, the in situ obtained CNT/MoSx nanocomposite catalyst is isolated from the interface and characterized by morphological and structural techniques. Moreover, the reaction kinetics for hydrogen production is calculated by real-time UV-vis absorption spectroscopy via measuring decamethylferrocenium concentrations. The hydrogen evolution reaction rate of CNT/MoSx increases by 85- and 2.5-fold compared with those of the uncatalyzed reaction and free-MoSx, respectively. The increased catalytic activity of CNT/MoSx is based on the enhanced charge transport efficiency of CNTs due to their one-dimensional (1D) structure, high electrical conductivity, excess active sites on MoSx, and the synergetic effect between CNTs and MoSx. This study paves the way for preparing nanocomposite catalysts with different substrates and also different energy applications using the CNT/MoSx nanocomposite catalyst.

Yazarlar (3)

1
Emre Aslan
2
Gizem Yanalak
3
Imren Hatay Patir
ORCID: 0000-0003-2937-6557

Anahtar Kelimeler

biphasic catalysis carbon nanotube electrodeposition energy conversion liquid/liquid interfaces

Kurumlar

Selçuk Üniversitesi
Selçuklu Turkey

Metrikler

10
Atıf
3
Yazar
5
Anahtar Kelime

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