Li Jinglin, Sheng Bowen, Chen Yiqing, Yang Jiajia, Wang Ping, Li Yixin, Yu Tianqi, Pan Hu, Song Jun, Zhu Lei, Wang Xinqiang, Ma Tao, 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, 200240, 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, 10087, China.
Small. 2024 Jun;20(25):e2309906. doi: 10.1002/smll.202309906. Epub 2024 Jan 14.
On-site hydrogen production from liquid organic hydrogen carriers e.g., methanol provides an emerging strategy for the safe storage and transportation of hydrogen. Herein, a catalytic architecture consisting of nickel-cobalt nanoclusters dispersed on gallium nitride nanowires supported by silicon for light-driven hydrogen production from methanol is reported. By correlative microscopic, spectroscopic characterizations, and density functional theory calculations, it is revealed that NiCo nanoclusters work in synergy with GaN nanowires to enable the achievement of a significantly reduced activation energy of methanol dehydrogenation by switching the potential-limiting step from *CHO → *CO to *CHO → *CHO. In combination with the marked photothermal effect, a high hydrogen rate of 5.62 mol·gcat-1·h-1 with a prominent turnover frequency of 43,460 h-1 is achieved at 5 Wcm-2 without additional energy input. Remarkably, the synergy between Co and Ni, in combination with the unique surface of GaN, renders the architecture with outstanding resistance to sintering and coking. The architecture thereby exhibits a high turnover number of >16,310,000 over 600 h. Outdoor testing validates the viability of the architecture for active and robust hydrogen evolution under natural concentrated sunlight. Overall, this work presents a promising architecture for on-site hydrogen production from CHOH by virtually unlimited solar energy.
通过液体有机氢载体(如甲醇)进行现场制氢为氢气的安全储存和运输提供了一种新兴策略。在此,报道了一种催化结构,该结构由分散在氮化镓纳米线上的镍钴纳米团簇组成,氮化镓纳米线由硅支撑,用于光驱动甲醇制氢。通过相关的显微镜、光谱表征以及密度泛函理论计算表明,镍钴纳米团簇与氮化镓纳米线协同作用,通过将限速步骤从*CHO → CO切换为CHO → *CHO,实现了甲醇脱氢活化能的显著降低。结合显著的光热效应,在5 Wcm-2的条件下,无需额外能量输入,即可实现5.62 mol·gcat-1·h-1的高析氢速率以及43,460 h-1的突出周转频率。值得注意的是,钴和镍之间的协同作用,再加上氮化镓独特的表面,使得该结构具有出色的抗烧结和抗结焦性能。因此,该结构在600小时内表现出大于16,310,000的高周转数。户外测试验证了该结构在自然聚光阳光下进行高效稳定析氢的可行性。总体而言,这项工作展示了一种通过几乎无限太阳能从甲醇现场制氢的有前景的结构。