Interface engineering of porous nickel-iron phosphates with enriched oxygen vacancies as an efficient bifunctional electrocatalyst for high current water splitting

被引:17
作者
Wang, Lixia [1 ]
Yu, Hongbo [1 ]
Huang, Zhiyang [1 ]
Luo, Zuyang [1 ]
Isimja, Tayirjan Taylor [3 ]
Xu, Shoulei [2 ]
Yang, Xiulin [1 ]
机构
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, Guangxi Key Lab Low Carbon Energy Mat, Guilin 541004, Peoples R China
[2] Guangxi Univ, Sch Phys Sci & Technol, 100 East Daxue Rd, Nanning 530004, Peoples R China
[3] King Abdullah Univ Sci & Technol KAUST, Saudi Arabia Basic Ind Corp SAB, Thuwal 239556900, Saudi Arabia
基金
中国国家自然科学基金;
关键词
Nickel -iron phosphates; Oxygen vacancies; Bifunctional; Electrocatalyst; Overall water splitting; EVOLUTION;
D O I
10.1016/j.electacta.2023.141932
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The delicate design of non-precious metal-based bifunctional electrocatalysts for simultaneous oxygen/hydrogen evolution reactions is pivotal for developing green and sustainable energy sources. Here, we have fabricated a novel nickel-iron phosphate heterostructure with abundant oxygen vacancies (Fe0.86Ni0.14-POx/CC) via hydro -thermal reaction and gas-phase phosphating treatment. By appropriately adjusting the ratio of Ni/Fe, the elec-tronic structure is regulated, thereby optimizing the oxygen vacancies to form abounded electrocatalytic active centers on the catalyst surface. The obtained Fe0.86Ni0.14-POx/CC catalyst reveals low overpotentials of 247 and 125 mV for OER and HER at a current density of 10 mA cm-2, respectively. Besides, the overall water splitting electrolyzer originated from Fe0.86Ni0.14-POx/CC only requires a cell voltage of 2.01 V to deliver a current density of 500 mA cm-2 with good stability of 100 h (10 mA cm-2). Importantly, Fe0.86Ni0.14-POx/CC possess 96.9 and 97.7% Faradaic yield for the generation of H2 and O2, respectively. This work invokes new feasibility for developing robust and cost-effective phosphate catalysts for electrochemical overall water splitting.
引用
收藏
页数:9
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