Mn-doped NiP: Facile synthesis and enhanced electrocatalytic activity for hydrogen evolution

被引:13
作者
Zhang, Changxin [1 ]
Li, Dan [2 ]
Xu, Yi [1 ]
机构
[1] Southwest Jiaotong Univ, Sch Mat Sci & Engn, Educ Minist, Key Lab Adv Technol Mat, Chengdu 610031, Peoples R China
[2] Sichuan Changhong Elect Holding Grp Co Ltd, New Energy Mat Lab, Chengdu 610041, Peoples R China
关键词
Mn; Dopant; Compound; Powder; Catalytic; Energy generation; SEMIMETALLIC WP2; NANOSHEET ARRAY; CARBON CLOTH; ONE-POT; EFFICIENT; SURFACE; NI2P; COP; NANOPARTICLES; ELECTRODES;
D O I
10.1557/s43578-021-00479-w
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Transition metal phosphides are considered to be inexpensive and effective catalysts for hydrogen evolution reaction. Here, the porous nickel powder was used as the matrix, and the second metal manganese was doped into porous nickel powder and red phosphorus powder. After being treated high-temperature phosphating, a kind of multiphase nickel phosphide (Ni3P, Ni2P, Ni12P5) catalyst material (Mn-NiP) with bimetallic composition was constructed. The activity of the catalyst doped with an appropriate amount of Mn increased owing to the regulation effect of doped Mn on the electronic structure of Ni and the mutual electronic interaction between Ni and P. The hydrogen evolution activity of 3Mn-NiP in the full pH range was mainly explored. The results showed that the overpotentials required for generating 10 mA.cm(-2) current density of 3Mn-NiP in 0.5 M H2SO4 and 1.0 M KOH were 164 and 77 mV, respectively. It showed better HER activity in an alkaline environment.
引用
收藏
页码:807 / 817
页数:11
相关论文
共 51 条
[1]   Catalytic hydrodenitrogenation of propionitrile over supported nickel phosphide catalysts as a model reaction for the transformation of pyrolysis oil obtained from animal by-products [J].
Badari, Cecilia A. ;
Lonyi, Ferenc ;
Dobe, Sandor ;
Hancsok, Jeno ;
Valyon, Jozsef .
REACTION KINETICS MECHANISMS AND CATALYSIS, 2015, 115 (01) :217-230
[2]   Dibenzothiophene hydrodesulfurization over cobalt phosphide catalysts prepared through a new synthetic approach: Effect of the support [J].
Cecilia, J. A. ;
Infantes-Molina, A. ;
Rodriguez-Castellon, E. ;
Jimenez-Lopez, A. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2009, 92 (1-2) :100-113
[3]  
Crolet JL, 1995, REV METALL-PARIS, V92, P1341
[4]   Computational and Experimental Study of Fluorine Doped (Mn1-xNbx)O2 Nanorod Electrocatalysts for Acid-Mediated Oxygen Evolution Reaction [J].
Ghadge, Shrinath Dattatray ;
Velikokhatnyi, Oleg I. ;
Datta, Moni K. ;
Shanthi, Pavithra M. ;
Tan, Susheng ;
Kumta, Prashant N. .
ACS APPLIED ENERGY MATERIALS, 2020, 3 (01) :541-557
[5]   Crystalline Copper Phosphide Nanosheets as an Efficient Janus Catalyst for Overall Water Splitting [J].
Han, Ali ;
Zhang, Hanyu ;
Yuan, Ruihan ;
Ji, Hengxing ;
Du, Pingwu .
ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (03) :2240-2248
[6]   Facile synthesis of Ni3S2/rGO nanosheets composite on nickel foam as efficient electrocatalyst for hydrogen evolution reaction in alkaline media [J].
He, Binhong ;
Zhou, Minjie ;
Hou, Zhaohui ;
Li, Gangyong ;
Kuang, Yafei .
JOURNAL OF MATERIALS RESEARCH, 2018, 33 (05) :519-527
[7]   NiSx@MoS2 heterostructure prepared by atomic layer deposition as high-performance hydrogen evolution reaction electrocatalysts in alkaline media [J].
He, Zuyun ;
Guo, Zheng ;
Wa, Qingbo ;
Zhong, Xiao ;
Wang, Xinwei ;
Chen, Yan .
JOURNAL OF MATERIALS RESEARCH, 2020, 35 (07) :822-830
[8]   Single-Crystal Nitrogen-Rich Two-Dimensional Mo5N6 Nanosheets for Efficient and Stable Seawater Splitting [J].
Jin, Huanyu ;
Liu, Xin ;
Vasileff, Anthony ;
Jiao, Yan ;
Zhao, Yongqiang ;
Zheng, Yao ;
Qiao, Shi-Zhang .
ACS NANO, 2018, 12 (12) :12761-12769
[9]  
Kibsgaard J, 2012, NAT MATER, V11, P963, DOI [10.1038/NMAT3439, 10.1038/nmat3439]
[10]   Multi-walled carbon nanotubes reinforced nickel phosphide composite: As an efficient electrocatalyst for hydrogen evolution reaction by one-step powder sintering [J].
Lan, Wei ;
Li, Dan ;
Wang, Wanxin ;
Liu, Zhongqing ;
Chen, Hui ;
Xu, Yi .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2020, 45 (01) :412-423