Li Jinglin, Sheng Bowen, Chen Yiqing, Yang Jiajia, Wang Ping, Li Yixin, Yu Tianqi, Pan Hu, Qiu Liang, Li Ying, Song Jun, Zhu Lei, Wang Xinqiang, Huang Zhen, Zhou Baowen
Key Laboratory for Power Machinery and Engineering of Ministry of Education, Research Center for Renewable Synthetic Fuel, School of Mechanical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai, China.
State Key Laboratory of Artificial Microstructure and Mesoscopic Physics, School of Physics, Nano-Optoelectronics Frontier Center of Ministry of Education (NFC-MOE), Peking University, Beijing, China.
Nat Commun. 2024 Aug 27;15(1):7393. doi: 10.1038/s41467-024-51810-y.
Photo-thermal-coupling ammonia decomposition presents a promising strategy for utilizing the full-spectrum to address the H storage and transportation issues. Herein, we exhibit a photo-thermal-catalytic architecture by assembling gallium nitride nanowires-supported ruthenium nanoparticles on a silicon for extracting hydrogen from ammonia aqueous solution in a batch reactor with only sunlight input. The photoexcited charge carriers make a predomination contribution on H activity with the assistance of the photothermal effect. Upon concentrated light illumination, the architecture significantly reduces the activation energy barrier from 1.08 to 0.22 eV. As a result, a high turnover number of 3,400,750 is reported during 400 h of continuous light illumination, and the H activity per hour is nearly 1000 times higher than that under the pure thermo-catalytic conditions. The reaction mechanism is extensively studied by coordinating experiments, spectroscopic characterizations, and density functional theory calculation. Outdoor tests validate the viability of such a multifunctional architecture for ammonia decomposition toward H under natural sunlight.
光热耦合氨分解为利用全光谱解决氢存储和运输问题提供了一种很有前景的策略。在此,我们展示了一种光热催化结构,通过在硅上组装氮化镓纳米线负载的钌纳米颗粒,在仅输入太阳光的间歇式反应器中从氨水溶液中提取氢气。光激发的电荷载流子在光热效应的辅助下对氢活性起主要作用。在聚光光照下,该结构将活化能垒从1.08 eV显著降低至0.22 eV。结果,在400小时的连续光照期间报告了高达3,400,750的高周转数,且每小时的氢活性比纯热催化条件下高出近1000倍。通过协同实验、光谱表征和密度泛函理论计算对反应机理进行了广泛研究。户外测试验证了这种多功能结构在自然阳光下氨分解制氢的可行性。