Back to Search Start Over

2D Ni‐Naphthalene‐2,6‐Dicarboxylic Acid Metal‐Organic Framework as Electrocatalysts for Efficient Overall Water Splitting.

Authors :
Lee, Min Kyung
Choi, Sungkyun
Park, Hoonkee
Lee, Tae Hyung
Lee, Sol A.
Yang, Jin Wook
Ji, Su Geun
Cheon, Woo Seok
Ahn, Sang Hyun
Kim, Soo Young
Shokouhimehr, Mohammadreza
Kim, Jin Young
Jang, Ho Won
Source :
Energy Technology; Jul2023, Vol. 11 Issue 7, p1-10, 10p
Publication Year :
2023

Abstract

Two‐dimensional metal‐organic frameworks (MOFs) are regarded as promising electrocatalysts because of their high surface area and tunable compositions. Herein, a novel nickel‐based 2D MOF for efficient oxygen evolution reaction (OER) has been developed. Ni‐NDC MOF nanosheets (NDC = naphthalene‐2,6‐dicarboxylic acid) are successfully synthesized on a nickel foam (NF) through a surfactant‐assisted one‐step hydrothermal method. The resulting Ni‐NDC@NF possessing a high electrochemically active surface area of 3.06 mF cm−2 exhibits excellent OER performance with a low overpotential of 249 mV at 10 mA cm−2, a small Tafel slope of 74 mV dec−1, 100% faradaic efficiency, and long‐term stability of 24 h at least. For the application of a bifunctional catalyst, NiMo alloy is electrodeposited on the Ni‐NDC@NF to enhance hydrogen evolution reaction activity. The overall water splitting in a two‐electrode configuration of NiMo/Ni‐NDC@NF electrodes as both anode and cathode require only a 1.56 V for 20 mA cm−2. The photovoltaic‐electrocatalysis system powered by the tandem solar cell represents a high solar‐to‐hydrogen efficiency of ≈22%. This work will contribute to inspiring the design of novel MOF composite catalysts using vertically aligned 2D MOF nanosheet architecture, thereby enlarging the potential of MOFs on next‐generation electrocatalysts and energy devices. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21944288
Volume :
11
Issue :
7
Database :
Complementary Index
Journal :
Energy Technology
Publication Type :
Academic Journal
Accession number :
164878301
Full Text :
https://doi.org/10.1002/ente.202201203