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Sub-second ultrafast yet programmable wet-chemical synthesis.

Lin ZhangLi PengYuanchao LuXin MingYuxin SunXiaoyi XuYuxing XiaKai PangWenzhang FangNing HuangZhen XuYibin YingYingjun LiuYingchun FuChao Gao
Published in: Nature communications (2023)
Wet-chemical synthesis via heating bulk solution is powerful to obtain nanomaterials. However, it still suffers from limited reaction rate, controllability, and massive consumption of energy/reactants, particularly for the synthesis on specific substrates. Herein, we present an innovative wet-interfacial Joule heating (WIJH) approach to synthesize various nanomaterials in a sub-second ultrafast, programmable, and energy/reactant-saving manner. In the WIJH, Joule heat generated by the graphene film (GF) is confined at the substrate-solution interface. Accompanied by instantaneous evaporation of the solvent, the temperature is steeply improved and the precursors are concentrated, thereby synergistically accelerating and controlling the nucleation and growth of nanomaterials on the substrate. WIJH leads to a record high crystallization rate of HKUST-1 (~1.97 μm s -1 ), an ultralow energy cost (9.55 × 10 -6  kWh cm -2 ) and low precursor concentrations, which are up to 5 orders of magnitude faster, -6 and -2 orders of magnitude lower than traditional methods, respectively. Moreover, WIJH could handily customize the products' amount, size, and morphology via programming the electrified procedures. The as-prepared HKUST-1/GF enables the Joule-heating-controllable and low-energy-required capture and liberation towards CO 2 . This study opens up a new methodology towards the superefficient synthesis of nanomaterials and solvent-involved Joule heating.
Keyphrases
  • ionic liquid
  • molecular dynamics simulations
  • heat stress
  • solid state
  • structural basis
  • walled carbon nanotubes