TY - JOUR
T1 - Ultrafine ruthenium-iridium alloy nanoparticles well-dispersed on N-rich carbon frameworks as efficient hydrogen-generation electrocatalysts
AU - Yu, Jie
AU - Dai, Yawen
AU - Wu, Xinhao
AU - Zhang, Zhenbao
AU - He, Qijiao
AU - Cheng, Chun
AU - Wu, Zhen
AU - Shao, Zongping
AU - Ni, Meng
N1 - Funding Information:
M. Ni thanks the funding support (Project Number: PolyU 152214/17E and PolyU 152064/18E) from Research Grant Council, University Grants Committee, Hong Kong SAR .
Publisher Copyright:
© 2020
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020
Y1 - 2020
N2 - The production of green energy, in this case, hydrogen (H2), from water electrolysis highly depends on the rational design of highly efficient yet cost-effective electrocatalysts for the hydrogen evolution reaction (HER). Precious-metal-based materials offer particularly prominent catalytic activities but suffer from the high cost. Thus, it is strongly desirable to develop low-metal-content composites as catalysts. In addition, fabricating an alloyed structure can greatly enhance the performance through synergy. Here, a novel nanohybrid of nanostructured RuIr alloys (~3.87 nm) with a low loading uniformly decorated on a highly porous and N-rich carbon matrix (RuIr@NrC) is constructed through a one-pot pyrolysis route. Taking advantage of the Ru/Ir single atoms, ultrafine RuIr nanostructure, high-porosity carbon substrate, and abundantly doped N, as well as their synergy, the as-formed composite demonstrates outstanding electrocatalytic performance for the HER under both basic and acidic conditions, with overpotentials of only 28 and 9 mV at 10 mA cm−2, respectively. Furthermore, the as-prepared RuIr@NrC exhibits robust durability for 2000 cycles. This structure outperforms its corresponding monometallic counterparts and many typical catalytic materials and is even comparable to commercial Pt/C. Notably, a high mass activity of 6.97 A mgnoble metal−1 is obtained, which is nearly ten times that of 20% Pt/C. This result shows the outstanding potential of RuIr@NrC for application in commercial water-splitting electrolyzers.
AB - The production of green energy, in this case, hydrogen (H2), from water electrolysis highly depends on the rational design of highly efficient yet cost-effective electrocatalysts for the hydrogen evolution reaction (HER). Precious-metal-based materials offer particularly prominent catalytic activities but suffer from the high cost. Thus, it is strongly desirable to develop low-metal-content composites as catalysts. In addition, fabricating an alloyed structure can greatly enhance the performance through synergy. Here, a novel nanohybrid of nanostructured RuIr alloys (~3.87 nm) with a low loading uniformly decorated on a highly porous and N-rich carbon matrix (RuIr@NrC) is constructed through a one-pot pyrolysis route. Taking advantage of the Ru/Ir single atoms, ultrafine RuIr nanostructure, high-porosity carbon substrate, and abundantly doped N, as well as their synergy, the as-formed composite demonstrates outstanding electrocatalytic performance for the HER under both basic and acidic conditions, with overpotentials of only 28 and 9 mV at 10 mA cm−2, respectively. Furthermore, the as-prepared RuIr@NrC exhibits robust durability for 2000 cycles. This structure outperforms its corresponding monometallic counterparts and many typical catalytic materials and is even comparable to commercial Pt/C. Notably, a high mass activity of 6.97 A mgnoble metal−1 is obtained, which is nearly ten times that of 20% Pt/C. This result shows the outstanding potential of RuIr@NrC for application in commercial water-splitting electrolyzers.
KW - A low metal loading
KW - Hydrogen evolution reaction
KW - N-rich carbon matrix
KW - The component synergy
KW - Ultrafine RuIr alloy
UR - http://www.scopus.com/inward/record.url?scp=85097876819&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2020.128105
DO - 10.1016/j.cej.2020.128105
M3 - Journal article
AN - SCOPUS:85097876819
SN - 1385-8947
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 128105
ER -