Stretchable,Transparent,and Ultra-Broadband Terahertz Shielding Thin Films Based on Wrinkled MXene Architectures

With the increasing demand for terahertz(THz)technology in security inspection,medical imaging,and flexible electronics,there is a significant need for stretchable and transparent THz electromagnetic interference(EMI)shielding materials.Existing EMI shielding materials,like opaque metals and carbon-based films,face challenges in achieving both high transparency and high shielding efficiency(SE).Here,a wrinkled structure strategy was proposed to construct ultra-thin,stretchable,and transparent terahertz shielding MXene films,which possesses both isotropous wrinkles(height about 50 nm)and periodic wrinkles(height about 500 nm).Compared to flat film,the wrinkled MXene film(8 nm)demonstrates a remarkable 36.5%increase in SE within the THz band.The wrinkled MXene film exhibits an EMI SE of 21.1 dB at the thickness of 100 nm,and an average EMI SE/t of 700 dBμm^(−1)over the 0.1-10 THz.Theoretical calculations suggest that the wrinkled structure enhances the film’s conductivity and surface plasmon resonances,resulting in an improved THz wave absorption.Additionally,the wrinkled structure enhances the MXene films’stretchability and stability.After bending and stretching(at 30%strain)cycles,the average THz transmittance of the wrinkled film is only 0.5%and 2.4%,respectively.The outstanding performances of the wrinkled MXene film make it a promising THz electromagnetic shielding materials for future smart windows and wearable electronics.

Co_(3)O_(4) with ordered pore structure derived from wood vessels for efficient Hg^(0) oxidation

Catalytic oxidation of Hgo to Hg~O is an efficient way to remove Hg^(0) from coal-fired flue gas.The catalyst with ordered pore structure can lower mass transfer resistance resulting in higher Hg^(0) oxidation efficiency.Therefore,in the present work,wood vessels were used as sacrificial template to obtain Co_(3)O_(4) with ordered pore structure.SEM and BET results show that,when the mass concentrations of Co(NO_(3))_(2)·6H_(2)O was 20%,the obtained catalyst(Co_(3)O_(4) [20%Co(NO_(3))_(2)])possesses better pore structure and higher surface area.It will expose more available surface active sites and lower the mass transfer resistance.Furthermore,XPS results prove that Co_(3)O_(4) [20%Co(NO_(3))_(2)]has the highest ratio of chemisorbed oxygen which plays an important role in Hg^(0) oxidation process.These results lead to a better Hg^(0) oxidation efficiency of Co_(3)O_(4) [20%Co(NO_(3))_(2)],which is about 90%in the temperature range of 200 to 350℃,Furthermore,Co_(3)O_(4) [20%Co(NO_(3))_(2)]has a stable catalytic activity,and its Hg^(0) oxidation efficiency maintains above 90%at 250℃even after 90 h test,A probable reaction mechanism is deduced by the XPS results of the fresh,used and regenerated catalyst of Co_(3)O_(4) [20%Co(NO3)2].Chemisorbed oxygen can react with Hg^(0) forming HgO with the reduction of Co^(3+)to Co^(2)+.And lattice oxygen and gaseous oxygen can supplement the consumption of chemisorbed oxygen to oxidize Co^(2+)to Co^(3+).