Single-atomic ruthenium coupling with NiFe layered double hydroxide in-situ growth on BiVO4 photoanode for boosting photoelectrochemical water splitting

被引:15
|
作者
Sun, Yunshuyu [1 ,2 ]
Li, Hao [1 ,2 ]
Hu, Yao [1 ,2 ]
Wang, Jinnan [1 ,2 ]
Li, Aimin [1 ,2 ]
Corvini, Philippe Francois- Xavier [3 ]
机构
[1] Nanjing Univ, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Peoples R China
[2] Nanjing Univ, Sch Environm, Nanjing 210023, Peoples R China
[3] Univ Appl Sci & Arts Northwestern Switzerland, Sch Life Sci, CH-4132 Basel, Switzerland
基金
中国国家自然科学基金;
关键词
Single-atomic Ru; NiFe Layered Double Hydroxide; BiVO4; photoanode; Photoelectrochemical water splitting; Oxygen evolution reaction; TOTAL-ENERGY CALCULATIONS; EVOLUTION; PERFORMANCE; STABILITY; CATALYSTS; INSIGHTS; TRENDS;
D O I
10.1016/j.apcatb.2023.123269
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
In the present work, NiFe layered double hydroxide (LDH) supported single Ru atoms in-situ growth on BiVO4 photoanode (BiVO4@NiFe-LDHs/Ru) was fabricated to enhance the photoelectrochemical (PEC) water splitting. Ru atoms anchored to NiFe-LDHs via oxygen coordination to form Ru-O-M bonds, which induced electrons rearrangement to improve charge carriers separation and injection. Combining with the synergistic effect of Ru and NiFe-LDHs, BiVO4@NiFe-LDHs/Ru achieves high photocurrent density of 4.65 mA/cm2 at 1.23 V vs. RHE. Besides, Ru atoms induced formation of V(5-x)+ to stabilize V atoms in the lattice of BiVO4, which avoided V5+ dissolution during PEC water oxidation process. Density functional theory (DFT) calculation indicates that Ru SAs anchored to BiVO4@NiFe-LDHs decrease the reaction energy barrier of rate-limiting step (*O & RARR; *OOH), resulting in acceleration of OER process. This work provides an effective pathway to design high efficient and stable photoanodes with single atoms for feasible PEC water splitting application.
引用
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页数:11
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