Zhang Lijie, Zhuang Linzhou, Liu Hongli, Zhang Longzhou, Cai Rongsheng, Chen Ning, Yang Xianfeng, Zhu Zhonghua, Yang Dongjiang, Yao Xiangdong
School of Environmental Science and Engineering State Key Laboratory of Bio-fibers and Eco-textiles Collaborative Innovation Center of Marine Biobased Fibers and Ecological Textiles Institute of Marine Biobased Materials Qingdao University Qingdao 266071 P. R. China.
School of Chemical Engineering The University of Queensland Brisbane 4072 Australia.
Small Sci. 2021 Mar 6;1(4):2000027. doi: 10.1002/smsc.202000027. eCollection 2021 Apr.
Water electrolysis is a promising option for pure hydrogen production, but it is limited by the high cost. Developing superb and low-cost electrocatalysts for hydrogen evolution reaction (HER) is critical for cost reduction. Heterostructures are demonstrated with excellent HER activities, but still inferior to commercial Pt/C. Herein, vacancy type of defects is engineered into the interface of CoP/NiP heterostructure by a plasma strategy. The as-synthesized defective CoP/NiP exhibits lower overpotentials than Pt/C. Its specific activity at overpotential of 50 mV is ≈2-fold and 1.7-fold higher than that of Pt/C in acidic and alkaline media, respectively. For water electrocatalysis, its current density reaches 215 mA cm at 2.0 V, even satisfying the target of practical industrial water splitting. Theoretical calculations indicate that the interfacial defects reconstruct the electronic structure and accelerate the charge transfer, facilitating the adsorption of reactant and lowering the energy barrier of water dissociation, thereby improving HER activities.
水电解是一种很有前景的纯氢生产方法,但它受到高成本的限制。开发用于析氢反应(HER)的优质低成本电催化剂对于降低成本至关重要。异质结构具有优异的HER活性,但仍不如商业Pt/C。在此,通过等离子体策略在CoP/NiP异质结构的界面上设计了空位型缺陷。合成的缺陷CoP/NiP表现出比Pt/C更低的过电位。其在50 mV过电位下的比活性在酸性和碱性介质中分别比Pt/C高约2倍和1.7倍。对于水电催化,其在2.0 V时的电流密度达到215 mA cm,甚至满足实际工业水分解的目标。理论计算表明,界面缺陷重构了电子结构并加速了电荷转移,促进了反应物的吸附并降低了水分解的能垒,从而提高了HER活性。