Jin Huanyu, Wang Xuesi, Tang Cheng, Vasileff Anthony, Li Laiquan, Slattery Ashley, Qiao Shi-Zhang
School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
Adelaide Microscopy, The University of Adelaide, Adelaide, SA, 5005, Australia.
Adv Mater. 2021 Apr;33(13):e2007508. doi: 10.1002/adma.202007508. Epub 2021 Feb 24.
Electrocatalytic production of hydrogen from seawater provides a route to low-cost and clean energy conversion. However, the hydrogen evolution reaction (HER) using seawater is greatly hindered by the lack of active and stable catalysts. Herein, an unsaturated nickel surface nitride (Ni-SN@C) catalyst that is active and stable for the HER in alkaline seawater is prepared. It achieves a low overpotential of 23 mV at a current density of 10 mA cm in alkaline seawater electrolyte, which is superior to Pt/C. Compared to conventional transition metal nitrides or metal/metal nitride heterostructures, the Ni-SN@C has no detectable bulk nickel nitride phase. Instead, unsaturated NiN bonding on the surface is present. In situ Raman measurements show that the Ni-SN@C performs like Pt with the ability to generate hydronium ions in a high-pH electrolyte. The catalyst operation is then demonstrated in a two-electrode electrolyzer system, coupling with hydrazine oxidation at the anode. Using this system, a cell voltage of only 0.7 V is required to achieve a current density of 1 A cm .
从海水中电催化制氢为低成本和清洁能源转换提供了一条途径。然而,使用海水的析氢反应(HER)因缺乏活性和稳定的催化剂而受到极大阻碍。在此,制备了一种在碱性海水中对HER具有活性和稳定性的不饱和镍表面氮化物(Ni-SN@C)催化剂。在碱性海水电解质中,当电流密度为10 mA cm 时,它实现了23 mV的低过电位,优于Pt/C。与传统的过渡金属氮化物或金属/金属氮化物异质结构相比,Ni-SN@C没有可检测到的块状氮化镍相。相反,表面存在不饱和的NiN键。原位拉曼测量表明,Ni-SN@C的性能类似于Pt,能够在高pH值电解质中产生水合氢离子。然后在两电极电解槽系统中展示了该催化剂的运行情况,并与阳极的肼氧化反应相耦合。使用该系统,仅需0.7 V的电池电压就能实现1 A cm 的电流密度。