氢气(H2)具有能量密度高、环境友好等优点,是一种很有前景的清洁能源载体.目前,电催化水裂解大规模制氢被认为是一种理想可行的方法.析氢反应(HER)涉及多个步骤,首先形成吸附的氢(Volmer步骤),然后是脱附步骤(Heyrovsky步骤)或两个相邻的吸附氢形成H2(Tafel步骤).与酸性介质相比,碱性介质中的HER可与现有的析氧反应(OER)催化剂偶合,降低电解水的设备成本,因此研究碱性条件下HER更具应用价值.但是,HER在碱性介质中不可避免地需要打破较强的共价键H-O-H,动力学缓慢,导致需要高过电位驱动反应.因此,开发适用于广泛的pH范围,特别是碱性介质高催化活性的催化剂,成为当务之急.金属铂是最高效的HER催化剂,但昂贵的价格严重阻碍了其在电解水中的大规模商业化应用.因此,开发过电位低和稳定性持久的非贵金属催化剂,特别是可以在大电流密度(＞500 mA cm-2的质子交换膜和碱性电解槽)下稳定工作的催化剂,对实际工业应用至关重要.过渡金属磷化物(TMPs),尤其是CoP和Ni2P在HER中表现出了较好的催化活性,引起广泛关注.但是,有限的电子结构、低电导率和大电流密度测试过程中的团聚仍然是限制其实际应用的瓶颈.近年来,具有金属可调性、多孔型结构、高比表面积和多交叉开放通道的金属有机骨架(MOFs)已被证明是制备TMPs的理想前驱体.但是,在高温煅烧过程中无法避免MOF结构坍塌,导致开放通道和电导率降低,限制了电子/离子的传输以及在高电流密度下的电催化活性.本文通过TMPs和Co-MOF之间的简单拓扑化学转化制备了一种自支撑结构的N掺杂二元TMPs电催化剂(N-CoPx/Ni2P),以Co-MOF作为模板和前驱体,一部分泡沫镍原位磷化成Ni2P,形成异质结构的双金属磷化物.扫描电镜和透射电镜结果表明,该催化剂呈三维多孔结构,有利于充分暴露活性位点.通过X射线光电子能谱分析了催化剂表面化学状态,发现形成了Co-N键,说明N掺杂成功.通过电化学测试结果表明,N-CoPx/Ni2P在全pH范围内表现出较好的HER活性,尤其在碱性介质中,当电流密度为650 mA cm-2时,仅需要152 mV过电位.催化剂转化率为3.2 S-1,法拉第效率接近100％,该催化剂在200 mA cm-2电流密度下连续工作24 h无明显衰减.密度泛函理论计算表明,N-CoPx/Ni2P催化活性的增强归因于氮掺杂及双金属磷化物的协同作用提高了催化剂的本征活性位点,从而优化了氢吸附能和水结合能.综上,本文为廉价电催化剂的工业化应用提供了一种有前景的策略.“,”Hydrogen evolution reaction is a critical reaction in water splitting for hydrogen production.How-ever,developing effective and stable non-noble-metal electrocatalysts which work well at high current densities demanded by industry still remain great challenge.Herein,taking advantage of the highly tunable metal-organic framework (MOF) templates,nitrogen doped binary transition metal phosphides electrocatalysts (N-CoPx/Ni2P) with three-dimensional (3D) conductive network struc-ture were successfully synthesized.The 3D open porous channels could expose more catalytically active sites;nitrogen doping and the synergistic effect between CoP and Ni2P can increase the elec-tron density of Co atoms at active sites,further optimizing the Gibbs free energy of hydrogen (△GH*)and water (△GH2O).As a result,the obtained N-CoPx/Ni2P catalyst exhibits extraordinary electrocat-alytic activity in a wide pH range.Especially,it requires an extremely low overpotential of 152 mV to deliver a high current density of 650 mA cm 2 in alkaline media.This work may shed some light on the rational design of cheap electrocatalysts and electrode materials that work well at high cur-rent densities.