TY - JOUR
T1 - Nitrogen-doped phosphorene for electrocatalytic ammonia synthesis
AU - Xu, Guangrui
AU - Li, Hao
AU - Bati, Abdulaziz S.R.
AU - Bat-Erdene, Munkhjargal
AU - Nine, Md J.
AU - Losic, Dusan
AU - Chen, Yu
AU - Shapter, Joseph G.
AU - Batmunkh, Munkhbayar
AU - Ma, Tianyi
PY - 2020/8/21
Y1 - 2020/8/21
N2 - The rapid surface oxidation of phosphorene under ambient conditions is considered to be a serious issue for many applications, but is used here as a strategy to achieve efficient heteroatom doping. Highly crystalline nitrogen-doped phosphorene (N-phosphorene) is prepared using a combination of ball milling and microwave techniques. The prepared N-doped phosphorene nanosheets showed outstanding electrocatalytic performance as a new type of non-metallic catalyst for nitrogen (N2) to ammonia (NH3) conversion, with an NH3 yield rate and faradaic efficiency (FE) of up to 18.79 μg h-1 mgCAT-1 and 21.51%, respectively, at a low overpotential (0 V) versus the reversible hydrogen electrode (RHE). Density functional theory calculations revealed that the high nitrogen reduction reaction (NRR) FEs originate from the increased hydrophobicity at the N and O doped phosphorene surfaces, which in turn hinders the competing hydrogen evolution reaction (HER) in an alkaline environment and promotes the NRR. This work not only introduces an efficient strategy to chemically functionalize 2D phosphorene, but also opens a new avenue in using N-doped phosphorene nanosheets as a metal-free catalyst.
AB - The rapid surface oxidation of phosphorene under ambient conditions is considered to be a serious issue for many applications, but is used here as a strategy to achieve efficient heteroatom doping. Highly crystalline nitrogen-doped phosphorene (N-phosphorene) is prepared using a combination of ball milling and microwave techniques. The prepared N-doped phosphorene nanosheets showed outstanding electrocatalytic performance as a new type of non-metallic catalyst for nitrogen (N2) to ammonia (NH3) conversion, with an NH3 yield rate and faradaic efficiency (FE) of up to 18.79 μg h-1 mgCAT-1 and 21.51%, respectively, at a low overpotential (0 V) versus the reversible hydrogen electrode (RHE). Density functional theory calculations revealed that the high nitrogen reduction reaction (NRR) FEs originate from the increased hydrophobicity at the N and O doped phosphorene surfaces, which in turn hinders the competing hydrogen evolution reaction (HER) in an alkaline environment and promotes the NRR. This work not only introduces an efficient strategy to chemically functionalize 2D phosphorene, but also opens a new avenue in using N-doped phosphorene nanosheets as a metal-free catalyst.
KW - Phosphorene
KW - Heteroatom doping
KW - Nanosheets
UR - http://www.scopus.com/inward/record.url?scp=85091676442&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/DE150101306
UR - http://purl.org/au-research/grants/ARC/LP160100927
UR - http://purl.org/au-research/grants/ARC/DP160101301
UR - http://purl.org/au-research/grants/ARC/IH150100003
U2 - 10.1039/d0ta03237a
DO - 10.1039/d0ta03237a
M3 - Article
AN - SCOPUS:85091676442
SN - 2050-7488
VL - 8
SP - 15875
EP - 15883
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 31
ER -