TY - JOUR
T1 - MOF-derived CoP-nitrogen-doped carbon@NiFeP nanoflakes as an efficient and durable electrocatalyst with multiple catalytically active sites for OER, HER, ORR and rechargeable zinc-air batteries
AU - Vijayakumar, E.
AU - Ramakrishnan, S.
AU - Sathiskumar, C.
AU - Yoo, Dong Jin
AU - Balamurugan, J.
AU - Noh, Hyun Sung
AU - Kwon, Dawool
AU - Kim, Young Hoon
AU - Lee, Haigun
N1 - Funding Information:
This research was supported by the BK21 FOUR Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education ( 4199990514635 ). This work was supported by the Materials and Components Technology Development Program of KEIT (Project No. 10053590 ).
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2022/1/15
Y1 - 2022/1/15
N2 - Highly active, long-lasting, and low-cost nanostructured catalysts with efficient oxygen evolution and oxygen reduction reactions (OER and ORR) are critical for achieving high-performance zinc-air batteries. Herein, we developed CoP-nitrogen-doped carbon@NiFeP nanoflakes (CoP-NC@NFP), derived from MOF enriched with multiple active sites, for multifunctional water splitting and zinc-air battery applications. The experimental results revealed that the multiple active catalytic sites of CoP-NC@NFP were responsible for the excellent charge-transfer kinetics and electrocatalytic performance with respect to water splitting. This performance is comparable to that of precious metal catalysts in alkaline electrolytes (OER: overpotential of 270 mV; HER: overpotential of 162 mV; ORR: Tafel slope of 46 mV dec−1; overall water splitting device: cell voltage of 1.57 V at 10 mA cm−2) with excellent electrochemical durability. Additionally, the structural stability of the OER and the HER durability of the CoP-NC@NFP electrocatalyst were confirmed by transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) studies. Most impressively, zinc-air batteries (ZABs) assembled with CoP-NC@NFP as the air–cathode exhibit exceptionally high power density of 93 mW cm−2 and prolonged operational stability over 200 h compared with a ZAB equipped with a benchmark air–cathode. The outcome of this study opens a practical possibility for the preparation of efficient multifunctional catalysts free of noble metals for clean energy production and storage.
AB - Highly active, long-lasting, and low-cost nanostructured catalysts with efficient oxygen evolution and oxygen reduction reactions (OER and ORR) are critical for achieving high-performance zinc-air batteries. Herein, we developed CoP-nitrogen-doped carbon@NiFeP nanoflakes (CoP-NC@NFP), derived from MOF enriched with multiple active sites, for multifunctional water splitting and zinc-air battery applications. The experimental results revealed that the multiple active catalytic sites of CoP-NC@NFP were responsible for the excellent charge-transfer kinetics and electrocatalytic performance with respect to water splitting. This performance is comparable to that of precious metal catalysts in alkaline electrolytes (OER: overpotential of 270 mV; HER: overpotential of 162 mV; ORR: Tafel slope of 46 mV dec−1; overall water splitting device: cell voltage of 1.57 V at 10 mA cm−2) with excellent electrochemical durability. Additionally, the structural stability of the OER and the HER durability of the CoP-NC@NFP electrocatalyst were confirmed by transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) studies. Most impressively, zinc-air batteries (ZABs) assembled with CoP-NC@NFP as the air–cathode exhibit exceptionally high power density of 93 mW cm−2 and prolonged operational stability over 200 h compared with a ZAB equipped with a benchmark air–cathode. The outcome of this study opens a practical possibility for the preparation of efficient multifunctional catalysts free of noble metals for clean energy production and storage.
KW - Metal organic framework
KW - Oxygen reduction reaction
KW - Transition metal phosphide
KW - Water splitting
KW - Zinc–air batteries
UR - http://www.scopus.com/inward/record.url?scp=85109527539&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2021.131115
DO - 10.1016/j.cej.2021.131115
M3 - Article
AN - SCOPUS:85109527539
SN - 1385-8947
VL - 428
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 131115
ER -