Zhang Fang-Shuai, Wang Jia-Wei, Luo Jun, Liu Rui-Rui, Zhang Zhi-Ming, He Chun-Ting, Lu Tong-Bu
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry , School of Chemistry , Sun Yat-Sen University , Guangzhou 510275 , China . Email:
Institute of New Energy Materials & Low Carbon Technology , School of Material Science & Engineering , Tianjin University of Technology , Tianjin 300384 , China . Email:
Chem Sci. 2017 Dec 21;9(5):1375-1384. doi: 10.1039/c7sc04569g. eCollection 2018 Feb 7.
The development of highly efficient, low-cost and stable electrocatalysts for overall water splitting is highly desirable for the storage of intermittent solar energy and wind energy sources. Herein, we show for the first time that nickel can be extracted from NiFe-layered double hydroxide (NiFe-LDH) to generate an NiP@FePO heterostructure. The NiP@FePO heterostructure was converted to an NiP@NiFe hydroxide heterostructure (P-NiFe) during water splitting, which displays high electrocatalytic performance for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in 1.0 M KOH solution, with an overpotential of 75 mV at 10 mA cm for HER, and overpotentials of 205, 230 and 430 mV at 10, 100 and 1000 mA cm for OER, respectively. Moreover, it could afford a stable current density of 10 mA cm for overall water splitting at 1.51 V in 1.0 M KOH with long-term durability (100 h). This cell voltage is among the best reported values for bifunctional electrocatalysts. The results of theoretical calculations demonstrate that P-NiFe displays optimized adsorption energies for both HER and OER intermediates at the nickel active sites, thus dramatically enhancing its electrocatalytic activity.
开发高效、低成本且稳定的用于全水解的电催化剂对于间歇性太阳能和风能的存储非常必要。在此,我们首次展示了可以从镍铁层状双氢氧化物(NiFe-LDH)中提取镍以生成NiP@FePO异质结构。在水分解过程中,NiP@FePO异质结构转变为NiP@NiFe氢氧化物异质结构(P-NiFe),其在1.0 M KOH溶液中对析氢反应(HER)和析氧反应(OER)均表现出高电催化性能,HER在10 mA cm时过电位为75 mV,OER在10、100和1000 mA cm时过电位分别为205、230和430 mV。此外,在1.0 M KOH中,它在1.51 V下可实现全水解的稳定电流密度为10 mA cm,且具有长期耐久性(100小时)。该电池电压是双功能电催化剂报道的最佳值之一。理论计算结果表明,P-NiFe在镍活性位点上对HER和OER中间体均表现出优化的吸附能,从而显著提高了其电催化活性。