Oxygen defect engineering on low-crystalline iron(iii) oxyhydroxide as a highly efficient electrocatalyst for water oxidation

被引:22
作者
Fan, Yaning [1 ]
Zhang, Junjun [1 ]
Luo, Kongliang [1 ]
Zhou, Xuanyu [1 ]
Zhao, Jiahua [2 ]
Bao, Weiwei [3 ]
Su, Hui [4 ]
Wang, Nailiang [1 ]
Zhang, Pengfei [1 ,2 ]
Luo, Zhenghong [1 ,2 ]
机构
[1] Ningxia Univ, Coll Chem & Chem Engn, State Key Lab High Efficiency Utilizat Coal & Gree, Yinchuan 750021, Ningxia, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[3] Shaanxi Univ Technol, Sch Mat Sci & Engn, Natl & Local Joint Engn Lab Slag Comprehens Utiliz, Hanzhong 723000, Shaanxi, Peoples R China
[4] McGill Univ, FRQNT Ctr Green Chem & Catalysis, Dept Chem, 801 Sherbrooke St W, Montreal, PQ H3A 0B8, Canada
基金
中国国家自然科学基金;
关键词
EVOLUTION REACTION; NANOSHEETS; CATALYST; VACANCIES;
D O I
10.1039/d3qi02043f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Improving the water oxidation performance of non-precious nanoelectrocatalysts is the key to developing green hydrogen energy. Herein, we developed a simple method to synthesize FeOOH nanocatalysts with low crystallinity and oxygen vacancies (V-O). These catalysts demonstrate excellent electrocatalytic performance for water oxidation. The V-O-FeOOH catalyst exhibits an overpotential of 255 mV at 10 mA cm(-2) and maintains stability for more than 120 hours at a high current output (50 mA cm(-2)). DFT calculations show that the rate-determining step (RDS) of V-O-FeOOH and FeOOH is O* to OOH* (the Gibbs free energy (Delta G) of the RDS is 1.65 eV and 1.91 eV, respectively). This result indicates that V-O can effectively reduce the energy barrier from *O to *OOH of the OER process, thus improving the activity of the V-O-FeOOH nanocatalysts. Our focus was on utilizing one of the abundant metallic elements to fabricate defect-rich OER electrocatalysts with improved performance through a convenient one-step synthesis approach. This methodology shows great promise for the development of high-performance catalysts.
引用
收藏
页码:114 / 122
页数:9
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