TY - JOUR
T1 - Efficient electrocatalytic proton reduction on CoP nanocrystals embedded in microporous P, N Co-doped carbon spheres with dual active sites
AU - Boppella, Ramireddy
AU - Park, Jaemin
AU - Yang, Wooseok
AU - Tan, Jeiwan
AU - Moon, Jooho
N1 - Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2020/1
Y1 - 2020/1
N2 - A facile and scalable method is reported to develop CoP nanocrystals encapsulated in a P, N co-doped C matrix (PNC) as a highly efficient electrocatalyst for hydrogen evolution reaction (HER) in acidic and basic media. The synthesized CoP-PNC electrocatalysts exhibit large specific surface area of 1543 m2 g−1, hierarchical microporous structure, and high density of surface -active sites. The porous CoP-PNC electrocatalysts exhibit excellent HER electroactivity, delivering a current density of 10 mA cm−2 at very low overpotentials of 87 and 106 mV in 0.5 M H2SO4 and 1 M KOH electrolytes, respectively. This remarkable HER performance mainly arises from the synergic effect between CoP and P, N co-doped C, high density of active sites and large surface area due to the multiple pore structures. Most importantly, the CoP-PNC retains high stability even after 40 h of continuous electrolysis in extremely acidic (pH = 0) and basic solutions (pH = 14).
AB - A facile and scalable method is reported to develop CoP nanocrystals encapsulated in a P, N co-doped C matrix (PNC) as a highly efficient electrocatalyst for hydrogen evolution reaction (HER) in acidic and basic media. The synthesized CoP-PNC electrocatalysts exhibit large specific surface area of 1543 m2 g−1, hierarchical microporous structure, and high density of surface -active sites. The porous CoP-PNC electrocatalysts exhibit excellent HER electroactivity, delivering a current density of 10 mA cm−2 at very low overpotentials of 87 and 106 mV in 0.5 M H2SO4 and 1 M KOH electrolytes, respectively. This remarkable HER performance mainly arises from the synergic effect between CoP and P, N co-doped C, high density of active sites and large surface area due to the multiple pore structures. Most importantly, the CoP-PNC retains high stability even after 40 h of continuous electrolysis in extremely acidic (pH = 0) and basic solutions (pH = 14).
UR - https://www.scopus.com/pages/publications/85072942147
U2 - 10.1016/j.carbon.2019.09.082
DO - 10.1016/j.carbon.2019.09.082
M3 - Article
AN - SCOPUS:85072942147
SN - 0008-6223
VL - 156
SP - 529
EP - 537
JO - Carbon
JF - Carbon
ER -