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Updated: Apr 13, 2026

Towards Biomimicking Wood: Fabricated Free-standing Films of Nanocellulose, Lignin, and a Synthetic Polycation
Published on: June 17, 2014
Oriented cellulose scaffold-based carbonized wood-supported phase change materials with stable morphology and high
Tao Zhang1, Juya Zhu1, Pei Yang1
1Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing 210037, China; International Innovation Center for Forest Chemicals and Materials, Nanjing 210037, China; Jiangsu Engineering Research Center of Fast-growing Trees and Agri-fiber Materials, Nanjing 210037, China.
Abstract:
Phase change materials are essential for sustainable thermal management, but challenges such as leakage, formability loss, low thermal conductivity, and poor photo-thermal conversion efficiency limit their stability and versatility. Herein, we propose a simple yet effective carbonization strategy that leverages the inherent three-dimensional, oriented, and hierarchical cellulose skeleton of carbonized wood (CW) to support polyethylene glycol (PEG). When the carbonization temperature is 1000 °C and the heating rate is 3-5 °C/min, the CW's maximum specific surface area and average pore diameter reach as high as 598.19 m2/g and 3.25 nm, respectively. Furthermore, the thermal conductivity of the CW-PEG composite phase change energy storage materials (CW-PEG composite PCESMs) increases to 0.434 W/m·K. The CW-PEG composite PCESMs exhibit a melting enthalpy of 130.5 J/g and an energy storage efficiency of 99.8 %. The surface temperature variations captured by the infrared camera during the heating and cooling cycles underscore the outstanding solar energy conversion efficiency of CW-PEG composite PCESMs. Moreover, even after 50 cycles, the phase change enthalpy retains 95 %, highlighting the CW-PEG composite PCESMs promising potential for energy-efficient building materials and cold chain transportation.
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