TY - JOUR
T1 - Co-MoCx supported on N-doped CNTs for efficient hydrogen evolution reaction under alkaline medium conditions
AU - Shen, Weilin
AU - Suen, Dawson Wai Shun
AU - Sze, Eric Tung Po
AU - Chen, Xiao
AU - Liang, Changhai
AU - Tsang, Chi Wing
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/11/6
Y1 - 2023/11/6
N2 - The water splitting reaction has the potential to be a sustainable and environmentally friendly way of producing hydrogen as a fuel source, which is an important step in reducing our reliance on fossil fuels and mitigating climate change. Currently, most commonly used catalysts for water splitting are based on precious metals such as platinum and iridium, which are expensive and scarce. Therefore, finding new catalysts that are low-cost, abundant and efficient is of great importance for making water splitting economically viable on a large scale. It was found that pairing up Co nanoparticles (NPs) with MoCx boosted the hydrogen evolution reaction (HER) activity by more than 2-fold (η10 = 130 mV, Tafel slope = 156.08 mV dec−1), compared with the pure Co NPs supported on N-doped carbon (η10 = 337 mV) under alkaline medium conditions. Its activity is comparable to those of Pt single-atom catalysts (SACs) supported on a mesoporous carbon matrix. The good activity may be due to the modification of the D-band of Co by Mo doping and the relatively high electrochemically active surface area (ECSA) of 477.25 cm2, which is comparable to those of Ru SAC materials.
AB - The water splitting reaction has the potential to be a sustainable and environmentally friendly way of producing hydrogen as a fuel source, which is an important step in reducing our reliance on fossil fuels and mitigating climate change. Currently, most commonly used catalysts for water splitting are based on precious metals such as platinum and iridium, which are expensive and scarce. Therefore, finding new catalysts that are low-cost, abundant and efficient is of great importance for making water splitting economically viable on a large scale. It was found that pairing up Co nanoparticles (NPs) with MoCx boosted the hydrogen evolution reaction (HER) activity by more than 2-fold (η10 = 130 mV, Tafel slope = 156.08 mV dec−1), compared with the pure Co NPs supported on N-doped carbon (η10 = 337 mV) under alkaline medium conditions. Its activity is comparable to those of Pt single-atom catalysts (SACs) supported on a mesoporous carbon matrix. The good activity may be due to the modification of the D-band of Co by Mo doping and the relatively high electrochemically active surface area (ECSA) of 477.25 cm2, which is comparable to those of Ru SAC materials.
UR - http://www.scopus.com/inward/record.url?scp=85176254668&partnerID=8YFLogxK
U2 - 10.1039/d3nj03937d
DO - 10.1039/d3nj03937d
M3 - Article
AN - SCOPUS:85176254668
SN - 1144-0546
VL - 47
SP - 21024
EP - 21032
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 45
ER -