Unveiling the role of Zn dopants in NiFe phosphide nanosheet for oxygen evolution reaction

被引:13
作者
Kou, Chendong [1 ,2 ]
Han, Jingrui [1 ]
Wang, Haibin [1 ]
Han, Mei [1 ]
Liang, Hongyan [1 ,2 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
[2] Tianjin Univ, Key Lab Efficient Utilizat Low & Medium Grade Ener, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
Transition metal phosphide; Sacrificial dopant; Self-supported electrode; Oxygen evolution reaction; EFFICIENT ELECTROCATALYSTS; FE; NANOARRAYS; ARRAYS;
D O I
10.1016/j.pnsc.2023.03.001
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Transition metal phosphides have been recognized as promising electrocatalysts for oxygen evolution reaction (OER) due to their low cost and high activity. However, the insufficient exposed active region limited the OER performance. Recently, the introduction of sacrificial dopants has been considered an effective strategy to enlarge the surface area. Herein, the Zn dopants are introduced in NiFe phosphide (NiFeZnP) nanosheet, which work as the sacrificial dopants to generate more exposed active NiFe sites and promote the formation of the NiFeOOH active phase during OER process. The optimized Zn-doped NiFeP catalyst shows an overpotential of X203 mV to reach a current density of 10 mA cm-2 in 1 M KOH, and a stability of 100 h at 1000 mA cm-2. Overall, this work provides a sacrificial Zn doping strategy to prepare highly efficient OER electrocatalysts.
引用
收藏
页码:74 / 82
页数:9
相关论文
共 60 条
[1]   In Situ Formation of Nano Ni-Co Oxyhydroxide Enables Water Oxidation Electrocatalysts Durable at High Current Densities [J].
Abed, Jehad ;
Ahmadi, Shideh ;
Laverdure, Laura ;
Abdellah, Ahmed ;
O'Brien, Colin P. ;
Cole, Kevin ;
Sobrinho, Pedro ;
Sinton, David ;
Higgins, Drew ;
Mosey, Nicholas J. ;
Thorpe, Steven J. ;
Sargent, Edward H. .
ADVANCED MATERIALS, 2021, 33 (45)
[2]   NiMoFe and NiMoFeP as Complementary Electrocatalysts for Efficient Overall Water Splitting and Their Application in PV-Electrolysis with STH 12.3% [J].
Baek, Minki ;
Kim, Guan-Woo ;
Park, Taiho ;
Yong, Kijung .
SMALL, 2019, 15 (49)
[3]   Vertically-interlaced NiFeP/MXene electrocatalyst with tunable electronic structure for high-efficiency oxygen evolution reaction [J].
Chen, Jiexin ;
Long, Qingwu ;
Xiao, Kang ;
Ouyang, Ting ;
Li, Nan ;
Ye, Siyu ;
Liu, Zhao-Qing .
SCIENCE BULLETIN, 2021, 66 (11) :1063-1072
[4]   The applications of single-atom alloys in electrocatalysis: Progress and challenges [J].
Da, Yumin ;
Jiang, Rui ;
Tian, Zhangliu ;
Han, Xiaopeng ;
Chen, Wei ;
Hu, Wenbin .
SMARTMAT, 2023, 4 (01)
[5]   The importance of nickel oxyhydroxide deprotonation on its activity towards electrochemical water oxidation [J].
Diaz-Morales, Oscar ;
Ferrus-Suspedra, David ;
Koper, Marc T. M. .
CHEMICAL SCIENCE, 2016, 7 (04) :2639-2645
[6]   Sepaktakraw-like catalyst Mn-doped CoP enabling ultrastable electrocatalytic oxygen evolution at 100 mA.cm-2 in alkali media [J].
Fu, Wen-Ying ;
Lin, Yu-Xiao ;
Wang, Mao-Sen ;
Si, Si ;
Wei, Lu ;
Zhao, Xin-Sheng ;
Wei, Yong-Sheng .
RARE METALS, 2022, 41 (09) :3069-3077
[7]   Revisiting cyclic voltammetry and electrochemical impedance spectroscopy analysis for capacitance measurements [J].
Gharbi, Oumaima ;
Tran, Mai T. T. ;
Tribollet, Bernard ;
Turmine, Mireille ;
Vivier, Vincent .
ELECTROCHIMICA ACTA, 2020, 343
[8]   Self-Supported FeNiP Nanosheet Arrays as a Robust Bifunctional Electrocatalyst for Water Splitting [J].
Guo, Jiaqian ;
Zhan, Zhenxiang ;
Lei, Ting ;
Yin, Ping .
ACS APPLIED ENERGY MATERIALS, 2022, 5 (05) :5855-5866
[9]   Boosting hydrogen evolution on NiFeZn electrocatalyst by defect surface modulation using alkali etching [J].
Guo, Wenwu ;
Kim, Junhyeong ;
Kim, Hyunki ;
Kim, Soo Young ;
Ahn, Sang Hyun .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2023, 48 (06) :2090-2100
[10]   Raman and Infrared Spectroscopy of a and β Phases of Thin Nickel Hydroxide Films Electrochemically Formed on Nickel [J].
Hall, David S. ;
Lockwood, David J. ;
Poirier, Shawn ;
Bock, Christina ;
MacDougall, Barry R. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2012, 116 (25) :6771-6784