Electrochemically active surface area controls HER activity for FexNi100-x films in alkaline electrolyte

被引:107
作者
Bakovic, Sergio I. Perez [1 ]
Acharya, Prashant [1 ]
Watkins, Morgan [1 ]
Thornton, Hannah [1 ]
Hou, Shixuan [1 ]
Greenlee, Lauren F. [1 ]
机构
[1] Univ Arkansas, Ralph E Martin Dept Chem Engn, Fayetteville, AR 72701 USA
关键词
Electrodeposition; Iron; Nickel; Films; Alkaline; Hydrogen evolution reaction; Electrochemically active surface area; Intrinsic activity;
D O I
10.1016/j.jcat.2020.12.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis and electrocatalytic activity of FexNi100-x electrochemically deposited films were investigated. Films were evaluated for the hydrogen evolution reaction (HER) in alkaline media with respect to composition and electrochemically active surface area (ECSA). Results demonstrate that films of higher or equal Fe content had an ECSA tenfold greater than films with higher Ni. When normalized by geometric surface area, Fe50Ni50 films required the lowest overpotential of -390 mV to reach a current density of -10 mA cm(2). However, when normalized by the ECSA, intrinsic HER activity increases as Ni content increases. Tafel slope, ECSA, microscopy, and impedance spectroscopy analyses allow a decoupled analysis of surface area versus activity effects on overall measured HER activity. These analyses collectively demonstrate that the increase in electrocatalytic activity is attributed to the increase in ECSA and not to an enhancement in the intrinsic activity by Fe and Ni component interactions. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:104 / 112
页数:9
相关论文
共 52 条
[1]   Electrodeposited Ni dendrites with high activity and durability for hydrogen evolution reaction in alkaline water electrolysis [J].
Ahn, Sang Hyun ;
Hwang, Seung Jun ;
Yoo, Sung Jong ;
Choi, Insoo ;
Kim, Hyoung-Juhn ;
Jang, Jong Hyun ;
Nam, Suk Woo ;
Lim, Tae-Hoon ;
Lim, Taeho ;
Kim, Soo-Kil ;
Kim, Jae Jeong .
JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (30) :15153-15159
[2]   Electrochemical Growth of Surface Oxides on Nickel. Part 3: Formation of β-NiOOH in Relation to the Polarization Potential, Polarization Time, and Temperature [J].
Alsabet, Mohammad ;
Grden, Michal ;
Jerkiewicz, Gregory .
ELECTROCATALYSIS, 2015, 6 (01) :60-71
[3]   The role of the Auger parameter in XPS studies of nickel metal, halides and oxides [J].
Biesinger, Mark C. ;
Lau, Leo W. M. ;
Gerson, Andrea R. ;
Smart, Roger St. C. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2012, 14 (07) :2434-2442
[4]   Resolving surface chemical states in XPS analysis of first row transition metals, oxides and hydroxides: Cr, Mn, Fe, Co and Ni [J].
Biesinger, Mark C. ;
Payne, Brad P. ;
Grosvenor, Andrew P. ;
Lau, Leo W. M. ;
Gerson, Andrea R. ;
Smart, Roger St. C. .
APPLIED SURFACE SCIENCE, 2011, 257 (07) :2717-2730
[5]   X-ray photoelectron spectroscopic chemical state quantification of mixed nickel metal, oxide and hydroxide systems [J].
Biesinger, Mark C. ;
Payne, Brad P. ;
Lau, Leo W. M. ;
Gerson, Andrea ;
Smart, Roger St. C. .
SURFACE AND INTERFACE ANALYSIS, 2009, 41 (04) :324-332
[6]   Studies of the hydrogen evolution reaction on Raney nickel-molybdenum electrodes [J].
Birry, L ;
Lasia, A .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2004, 34 (07) :735-749
[7]   Current status of water electrolysis for energy storage, grid balancing and sector coupling via power-to-gas and power-to-liquids: A review [J].
Buttler, Alexander ;
Spliethoff, Hartmut .
RENEWABLE & SUSTAINABLE ENERGY REVIEWS, 2018, 82 :2440-2454
[8]   The hydrogen economy [J].
Crabtree, GW ;
Dresselhaus, MS ;
Buchanan, MV .
PHYSICS TODAY, 2004, 57 (12) :39-44
[9]   Electrochemical Hydrogen Evolution at Ordered Mo7Ni7 [J].
Csernica, Peter M. ;
McKone, James R. ;
Mulzer, Catherine R. ;
Dichtel, William R. ;
Abruna, Hector D. ;
DiSalvo, Francis J. .
ACS CATALYSIS, 2017, 7 (05) :3375-3383
[10]   Electrochemical and in situ magnetic study of iron/iron oxide films oxidized and reduced in KOH solution for magneto-ionic switching [J].
Duschek, K. ;
Uhlemann, M. ;
Schloerb, H. ;
Nielsch, K. ;
Leistner, K. .
ELECTROCHEMISTRY COMMUNICATIONS, 2016, 72 :153-156