TY - JOUR
T1 - Controllable Edge Exposure of MoS2 for Efficient Hydrogen Evolution with High Current Density
AU - Zhang, Zexia
AU - Wang, Yuanxi
AU - Leng, Xiangxing
AU - Crespi, Vincent H.
AU - Kang, Feiyu
AU - Lv, Ruitao
N1 - Funding Information:
The authors are grateful for the financial support from the National Natural Science Foundation of China (51722207), 973 program of China (2015CB932500), Beijing Nova Program (Z161100004916099), and the Tsinghua University Initiative Scientific Research Program (20151080367). Z.Z. acknowledges the financial support from the National Natural Science Foundation of China (11364043). Y. W. and V. H. C. acknowledge support from the National Science Foundation Materials Innovation Platform under DMR-1539916.
PY - 2018/3/26
Y1 - 2018/3/26
N2 - MoS2-based electrocatalysts are promising cost-effective replacements for Pt-based catalysts for hydrogen evolution by water splitting, yet achieving high current density at low overpotential remains a challenge. Herein, a binder-free electrode of MoS2/CNF (carbon nanofiber) is prepared by electrospinning and subsequent thermal treatment. The growth of MoS2 nanoplates contained within or protruding out from the CNF can be controlled by adding urea or ammonium bicarbonate to the electrospinning precursors, due to the cross-linking effects of urea and the increased porosity caused by pyrolysis of ammonium bicarbonate allowing growth through pores in the CNF. By virtue of the abundant exposed edges in this microstructure and strong bonding between the catalyst and the conductive carbon network, the composite material exhibits ultrahigh electrocatalytic hydrogen evolution activity in acidic solutions, with current densities of 500 and 1000 mA/cm2 at overpotentials of 380 and 450 mV, respectively, exceeding the performance of many reported MoS2-based catalysts and even commercial Pt/C catalysts. Thus, MoS2/CNF membranes show potential as efficient and flexible binder-free electrodes for electrocatalytic hydrogen production.
AB - MoS2-based electrocatalysts are promising cost-effective replacements for Pt-based catalysts for hydrogen evolution by water splitting, yet achieving high current density at low overpotential remains a challenge. Herein, a binder-free electrode of MoS2/CNF (carbon nanofiber) is prepared by electrospinning and subsequent thermal treatment. The growth of MoS2 nanoplates contained within or protruding out from the CNF can be controlled by adding urea or ammonium bicarbonate to the electrospinning precursors, due to the cross-linking effects of urea and the increased porosity caused by pyrolysis of ammonium bicarbonate allowing growth through pores in the CNF. By virtue of the abundant exposed edges in this microstructure and strong bonding between the catalyst and the conductive carbon network, the composite material exhibits ultrahigh electrocatalytic hydrogen evolution activity in acidic solutions, with current densities of 500 and 1000 mA/cm2 at overpotentials of 380 and 450 mV, respectively, exceeding the performance of many reported MoS2-based catalysts and even commercial Pt/C catalysts. Thus, MoS2/CNF membranes show potential as efficient and flexible binder-free electrodes for electrocatalytic hydrogen production.
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U2 - 10.1021/acsaem.8b00010
DO - 10.1021/acsaem.8b00010
M3 - Article
AN - SCOPUS:85058126138
SN - 2574-0962
VL - 1
SP - 1268
EP - 1275
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 3
ER -