Wei Peng, Zhuge Xiangqun, Li Qi, Sun Xueping, Liu Wenjun, Liang Kang, Han Jiantao, Ren Yurong, Huang Yunhui
School of Materials Science and Engineering, Jiangsu Province Engineering Research Center of Intelligent Manufacturing Technology for the New Energy Vehicle Power Battery, Changzhou University, Changzhou 213164, China; State Key Laboratory of Material Processing and Die & Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.
School of Materials Science and Engineering, Jiangsu Province Engineering Research Center of Intelligent Manufacturing Technology for the New Energy Vehicle Power Battery, Changzhou University, Changzhou 213164, China.
J Colloid Interface Sci. 2024 May 15;662:814-821. doi: 10.1016/j.jcis.2024.02.045. Epub 2024 Feb 8.
As a potential catalyst for hydrogen evolution reaction (HER), tungsten nitride (WN) has attracted extensive attention, due to its Pt-like characteristic. Nevertheless, insufficient active sites, slow electron transfer, and lack of scale-up nano-synthesis methods significantly limit its practical application. Constructing multi-component active centers and interface-rich heterojunctions to increase exposed active sites and modulate interface electrons is a very effective modification strategy. Therefore, a nano-heterostructure formed from tungsten nitride, tungsten phosphide and tungsten encapsulated in N, P co-doped carbon nanofiber (WN/WP/W@NPC) was synthesized by a flexible and scalable electrospinning technology. Experimental results reveal that abundant heterojunctions are formed, electron transfer occurs between tungsten nitride and tungsten phosphide, and carbon nanofibers play a confinement role. The optimized WN/WP/W@NPC-3 electrocatalyst demonstrates excellent HER catalytic activity and robust stability in both acidic and base media. Furthermore, the overall water splitting performance is tested using WN/WP/W@NPC as the cathode through a two-electrode electrolyzer, which also exhibits impressive electrochemical performance.
作为析氢反应(HER)的潜在催化剂,氮化钨(WN)因其类铂特性而备受关注。然而,活性位点不足、电子转移缓慢以及缺乏可放大的纳米合成方法严重限制了其实际应用。构建多组分活性中心和富含界面的异质结以增加暴露的活性位点并调节界面电子是一种非常有效的改性策略。因此,通过灵活且可扩展的静电纺丝技术合成了由氮化钨、磷化钨和包裹在氮、磷共掺杂碳纳米纤维(WN/WP/W@NPC)中的钨形成的纳米异质结构。实验结果表明,形成了大量异质结,氮化钨和磷化钨之间发生电子转移,并且碳纳米纤维起到限制作用。优化后的WN/WP/W@NPC-3电催化剂在酸性和碱性介质中均表现出优异的HER催化活性和稳健的稳定性。此外,使用WN/WP/W@NPC作为阴极通过双电极电解槽测试了整体水分解性能,其也表现出令人印象深刻的电化学性能。