Lu Fagui, Lu Kuan, Zhao Gui, Zhou Song, He Bowen, Zhang Yixiao, Xu Jian, Li Yongwang, Liu Xi, Chen Liwei
School of Chemistry and Chemical Engineering, In-situ Center for Physical Sciences, Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University Shanghai 200240 China
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences Taiyuan 030001 China.
RSC Adv. 2022 Jul 7;12(31):19869-19874. doi: 10.1039/d2ra03145k. eCollection 2022 Jul 6.
High-entropy alloys (HEAs) with multiple elements in near-equiatomic proportions hold great promise in heterogeneous catalysis because of their exceptional physicochemical properties governed by synergy. Herein, we prepared PtPdCoCuNi HEA nanoparticles a one-step colloid-based route and tested their catalytic performance for nitrobenzene hydrogenation to aniline. The SiO supported PtPdCoCuNi displays 93.9% yield of aniline at 80 °C, which is 2.11 times that of PtPd/SiO. Even at room temperature, a 47.4% yield of aniline is attained with the PtPdCoCuNi/SiO catalyst. DRIFTS experiments indicate formation of isolated Pt and Pd sites after alloying the transition metals and evidence a stronger interaction between the HEA catalyst and nitrobenzene. Both XPS data and DFT calculations disclose charge transfer to Pt and Pd species, which eventually enhance the interaction between nitrobenzene and the isolated metal sites and the hydrogenation activity as well. The experimental and theoretical results shed light on mechanistic understanding of the unique catalytic performance of the HEA nanocatalyst and pave a new avenue to realize the high catalytic performance of nitrobenzene hydrogenation over well-isolated noble metal sites with specific geometries.
具有近等原子比例多种元素的高熵合金(HEAs)由于其协同作用所决定的特殊物理化学性质,在多相催化领域具有巨大潜力。在此,我们通过一步胶体法制备了PtPdCoCuNi高熵合金纳米颗粒,并测试了它们对硝基苯加氢制苯胺的催化性能。SiO负载的PtPdCoCuNi在80°C时苯胺产率为93.9%,是PtPd/SiO的2.11倍。即使在室温下,PtPdCoCuNi/SiO催化剂的苯胺产率也能达到47.4%。漫反射红外傅里叶变换光谱(DRIFTS)实验表明,过渡金属合金化后形成了孤立的Pt和Pd位点,并证明了高熵合金催化剂与硝基苯之间存在更强的相互作用。X射线光电子能谱(XPS)数据和密度泛函理论(DFT)计算均揭示了电荷向Pt和Pd物种的转移,这最终增强了硝基苯与孤立金属位点之间的相互作用以及加氢活性。实验和理论结果有助于深入理解高熵合金纳米催化剂独特的催化性能,并为在具有特定几何结构的良好孤立贵金属位点上实现硝基苯加氢的高催化性能开辟了一条新途径。