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杭州 | 浙江大学杭州国际科创中心 | 科创百人计划研究员
  邮箱   wenzhang.fang@zju.edu.cn  电话   13564729048
论文

A mini review of nanomaterials on photodynamic therapy

期刊: Journal of Photochemistry and Photobiology C: Photochemistry Reviews  2023
作者: Chencheng Dong,Qiuying Yi,Wenzhang Fang,Jinlong Zhang
DOI:10.1016/j.jphotochemrev.2022.100568

Plasmonic Terahertz Devices and Sensors Based on Carbon Electronics

期刊: ACS Applied Materials & Interfaces  2023
作者: Wendao Xu,Wenzhang Fang,Teng Shi,Xin Ming,Yingli Wang,Lijuan Xie,Li Peng,Hou-Tong Chen,Yibin Ying
DOI:10.1021/acsami.2c22411

A review on graphene oxide: 2D colloidal molecule, fluid physics, and macroscopic materials

Graphene oxide (GO), a mostly known oxidized derivative of graphene, which possesses two-dimensional (2D) topological nature and good dispersity in multiple common solvents as a single layer, has shown unique molecular science and fluid physics. Assembling 2D GO macromolecules into a variety of carbonaceous architectures is recognized as an important nanotechnology to address the challenge of translating the unprecedented mechanical, electrical, and thermal properties of graphene into a macroscopic level. To realize real-world applications of graphene-based materials, sophisticated architecture manipulation spanning from the nanoscale, mesoscale to macroscale is essential to make sure every atom is at the right place. It takes comprehensive understanding of the compositional chemistry, fluid physics, and solid-state physics of 2D GO and graphene. Much effort in studying the graphene solid-state materials has helped people build perspectives on their structure-property relations. Nevertheless, the molecular science and fluid physics of GO that governs the single molecular behavior and collective effects of sheets still lack exploration. Single GO sheet exhibits both colloid behaviors and molecule conformations, which can be viewed as a 2D colloidal macromolecule with special dynamic aggregate and transition behaviors in solvents. Focusing on this topic, we have summarized recent progress in the science, technology, and engineering of 2D GO colloidal macromolecules with particular focus on intriguing features of molecular conformation, lyotropic liquid crystal, slow relaxation behavior, reversible fusion and fission, etc. Novel solvation-triggered hydroplastic processing for graphene-based macroscopic materials will be introduced, followed by the structural principles for high-performance graphene macroscopic materials. Finally, we will wrap up the topic with some perspectives on future research directions and give our opinions on the roadmap toward graphene industrialization.

期刊: Applied Physics Reviews  2023
作者: Fang Wang,Wenzhang Fang,Xin Ming,Yingjun Liu,Zhen Xu,Chao Gao
DOI:10.1063/5.0128899

Defect-induced photocurrent gain for carbon nanofilm-based broadband infrared photodetector

期刊: Carbon  2022
作者: Xiaoxue Cao,Li Peng,Lixiang Liu,Jianhang Lv,Zongwen Li,Feng Tian,Yunfan Dong,Xinyu Liu,Ying Shen,Haiyan Sun,Yang Xu,Wenzhang Fang,Chao Gao
DOI:10.1016/j.carbon.2022.07.028

Multifunctional Macroassembled Graphene Nanofilms with High Crystallinity

AbstractA “cooling–contraction” method to separate large‐area (up to 4.2 cm in lateral size) graphene oxide (GO)‐assembled films (of nanoscale thickness) from substrates is reported. Heat treatment at 3000 °C of such free‐standing macroscale films yields highly crystalline “macroassembled graphene nanofilms” (nMAGs) with 16–48 nm thickness. These nMAGs present tensile strength of 5.5–11.3 GPa (with ≈3 µm gauge length), electrical conductivity of 1.8–2.1 MS m−1, thermal conductivity of 2027–2820 W m−1 K−1, and carrier relaxation time up to ≈23 ps. As a demonstration application, an nMAG‐based sound‐generator shows a 30 µs response and sound pressure level of 89 dB at 1 W cm−2. A THz metasurface fabricated from nMAG has a light response of 8.2% for 0.159 W mm−2 and can detect down to 0.01 ppm of glucose. The approach provides a straightforward way to form highly crystallized graphene nanofilms from low‐cost GO sheets.

期刊: Advanced Materials  2021
作者: Li Peng,Ying Han,Meihui Wang,Xiaoxue Cao,Junfeng Gao,Yingjun Liu,Xianjue Chen,Bin Wang,Bo Wang,Chongyang Zhu,Xiao Wang,Ke Cao,Ming Huang,Benjamin V. Cunning,Jintao Pang,Wendao Xu,Yibin Ying,Zhen Xu,Wenzhang Fang,Yang Lu,Rodney S. Ruoff,Chao Gao
DOI:10.1002/adma.202104195

Gold-loaded graphene oxide/PDPB composites for the synchronous removal of Cr(VI) and phenol

期刊: Chinese Journal of Catalysis  2018
作者: Jun Liu,Wenzhang Fang,Yuhang Wang,Mingyang Xing,Jinlong Zhang
DOI:10.1016/s1872-2067(17)62933-4

Advanced Bi2O2.7/Bi2Ti2O7 composite film with enhanced visible-light-driven activity for the degradation of organic dyes

期刊: Research on Chemical Intermediates  2018
作者: Wenzhang Fang,Li Zhou,Bin Shen,Yi Zhou,Qiuying Yi,Mingyang Xing,Jinlong Zhang
DOI:10.1007/s11164-018-3268-5

Reduced {001}-TiO<sub>2−x</sub> photocatalysts: noble-metal-free CO<sub>2</sub> photoreduction for selective CH<sub>4</sub> evolution

The preparation of reduced TiO2 photocatalysts with high Ti3+ concentration is a great challenge due to their instability in air.

期刊: Physical Chemistry Chemical Physics  2017
作者: Wenzhang Fang,Lhoussain Khrouz,Yi Zhou,Bin Shen,Chunyang Dong,Mingyang Xing,Shashank Mishra,Stéphane Daniele,Jinlong Zhang
DOI:10.1039/c7cp01212h

Enhanced photocatalytic activities of vacuum activated TiO2 catalysts with Ti3+ and N co-doped

期刊: Catalysis Today  2016
作者: Wenzhang Fang,Yi Zhou,Chencheng Dong,Mingyang Xing,Jinlong Zhang
DOI:10.1016/j.cattod.2015.07.027

Highly-dispersed boron-doped graphene nanoribbons with enhanced conductibility and photocatalysis

B-GNRs, prepared by a simple vacuum activation method, have excellent conductivity and photocatalytic activity.

期刊: Chem. Commun.  2014
作者: Mingyang Xing,Wenzhang Fang,Xiaolong Yang,Baozhu Tian,Jinlong Zhang
DOI:10.1039/c4cc01341g

Self-doped Ti 3+ -enhanced TiO 2 nanoparticles with a high-performance photocatalysis

期刊: Journal of Catalysis  2013
作者: Mingyang Xing,Wenzhang Fang,Muhammad Nasir,Yunfei Ma,Jinlong Zhang,Masakazu Anpo
DOI:10.1016/j.jcat.2012.10.014

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