TY - JOUR
T1 - Ni/nitrogen-doped graphene nanotubes acted as a valuable tailor for remarkably enhanced hydrogen evolution performance of platinum-based catalysts
AU - Bao, Xiaobing
AU - Wang, Jing
AU - Lian, Xu
AU - Jin, Haiyan
AU - Wang, Shiping
AU - Wang, Yong
N1 - Publisher Copyright:
© 2017 The Royal Society of Chemistry.
PY - 2017
Y1 - 2017
N2 - Markedly minimizing the platinum (Pt) loading and increasing its mass activity are significant to drive down the cost of H2 production from water splitting. Herein, a novel electrocatalyst, Pt nanoparticles (NPs) anchored on Ni/nitrogen-doped graphene nanotubes (Pt/Ni@NGNTs), was designed and its exceptional catalytic performance towards hydrogen evolution reaction was demonstrated. Ni@NGNTs itself showed poor catalytic activity. Unexpectedly, when employed as a support, it increased the mass activity of the Pt metal by 30.1 times in an acidic electrolyte and 15.3 times in an alkaline electrolyte relative to that of commercial 20 wt% Pt/C. Moreover, the durability of Pt/Ni@NGNTs reached up to 50 h. Impressively, Pt NPs preferentially distributed around the protective graphene shells of the enclosed metal Ni, due to the enriched electron density and structural defects induced by Ni and N dopants. The electronic interactions between Pt and Ni@NGNTs tuned the electronic properties and greatly boosted catalytic performances of the anchored Pt NPs. The present catalyst shows significant potential for the synthesis of low cost, high performance Pt-based catalysts.
AB - Markedly minimizing the platinum (Pt) loading and increasing its mass activity are significant to drive down the cost of H2 production from water splitting. Herein, a novel electrocatalyst, Pt nanoparticles (NPs) anchored on Ni/nitrogen-doped graphene nanotubes (Pt/Ni@NGNTs), was designed and its exceptional catalytic performance towards hydrogen evolution reaction was demonstrated. Ni@NGNTs itself showed poor catalytic activity. Unexpectedly, when employed as a support, it increased the mass activity of the Pt metal by 30.1 times in an acidic electrolyte and 15.3 times in an alkaline electrolyte relative to that of commercial 20 wt% Pt/C. Moreover, the durability of Pt/Ni@NGNTs reached up to 50 h. Impressively, Pt NPs preferentially distributed around the protective graphene shells of the enclosed metal Ni, due to the enriched electron density and structural defects induced by Ni and N dopants. The electronic interactions between Pt and Ni@NGNTs tuned the electronic properties and greatly boosted catalytic performances of the anchored Pt NPs. The present catalyst shows significant potential for the synthesis of low cost, high performance Pt-based catalysts.
UR - http://www.scopus.com/inward/record.url?scp=85027122449&partnerID=8YFLogxK
U2 - 10.1039/c7ta01240c
DO - 10.1039/c7ta01240c
M3 - Article
AN - SCOPUS:85027122449
SN - 2050-7488
VL - 5
SP - 16249
EP - 16254
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 31
ER -