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Tailoring Transition‐Metal Hydroxides and Oxides by Photon‐Induced Reactions
Authors:Dr Kai‐Yang Niu  Prof?Dr Liang Fang  Rong Ye  Dr Dennis Nordlund  Dr Marca M Doeff  Prof?Dr Feng Lin  Dr Haimei Zheng
Institution:1. Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA;2. State Key Laboratory of Mechanical Transmission, College of Physics, Chongqing University, Chongqing, China;3. Department of Chemistry, University of California, Berkeley, CA, USA;4. Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, California, USA;5. Energy Storage and Distributed Resources Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA;6. Department of Chemistry, Virginia Tech, Blacksburg, VA, USA;7. Department of Materials Science and Engineering, University of California, Berkeley, CA, USA
Abstract:Controlled synthesis of transition‐metal hydroxides and oxides with earth‐abundant elements have attracted significant interest because of their wide applications, for example as battery electrode materials or electrocatalysts for fuel generation. Here, we report the tuning of the structure of transition‐metal hydroxides and oxides by controlling chemical reactions using an unfocused laser to irradiate the precursor solution. A Nd:YAG laser with wavelengths of 532 nm or 1064 nm was used. The Ni2+, Mn2+, and Co2+ ion‐containing aqueous solution undergoes photo‐induced reactions and produces hollow metal‐oxide nanospheres (Ni0.18Mn0.45Co0.37Ox) or core–shell metal hydroxide nanoflowers (Ni0.15Mn0.15Co0.7(OH)2](NO3)0.2?H2O), depending on the laser wavelengths. We propose two reaction pathways, either by photo‐induced redox reaction or hydrolysis reaction, which are responsible for the formation of distinct nanostructures. The study of photon‐induced materials growth shines light on the rational design of complex nanostructures with advanced functionalities.
Keywords:nanostructures  photochemistry  reaction pathways  transition-metal hydroxides  vibrational excitation
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