Mein Jin Tan

Towards lignin-based functional materials in a sustainable world

In light of the incessant consumption of raw materials in the world today, the search for sustainable resources is ever pressing. Lignin, the second most naturally abundant biomass, which makes up 15% to 35% of the cell walls of terrestrial plants, has always been treated as waste and used in low-value applications such as heat and electricity generation. However, its abundance in nature could potentially solve the problem of the rapidly depleting resources if it was successfully translated into a renewable resource or valorized to higher value materials. Advanced lignin modification chemistry has generated a number of functional lignin-based polymers, which integrate both the intrinsic features of lignin and additional properties of the grafted polymers. These modified lignin and its copolymers display better miscibility with other polymeric matrices, leading to improved performance for these lignin/polymer composites. This review summarizes the progress in using such biopolymers as reinforcement fillers, antioxidants, UV adsorbents, antimicrobial agents, carbon precursors and biomaterials for tissue engineering and gene therapy. Recent developments in lignin-based smart materials are discussed as well.

Nanoparticle–Hydrogel Composites: Concept, Design, and Applications of These Promising, Multi‐Functional Materials

New technologies rely on the development of new materials, and these may simply be the innovative combination of known components. The structural combination of a polymer hydrogel network with a nanoparticle (metals, non‐metals, metal oxides, and polymeric moieties) holds the promise of providing superior functionality to the composite material with applications in diverse fields, including catalysis, electronics, bio‐sensing, drug delivery, nano‐medicine, and environmental remediation. This mixing may result in a synergistic property enhancement of each component: for example, the mechanical strength of the hydrogel and concomitantly decrease aggregation of the nanoparticles. These mutual benefits and the associated potential applications have seen a surge of interest in the past decade from multi‐disciplinary research groups. Recent advances in nanoparticle–hydrogel composites are herein reviewed with a focus on their synthesis, design, potential applications, and the inherent challenges accompanying these exciting materials.

Air-Stable Efficient Inverted Polymer Solar Cells Using Solution-Processed Nanocrystalline ZnO Interfacial Layer

In this work, efficient bulk heterojunction (BHJ) organic solar cells (OSC) in inverted configuration have been demonstrated. Power conversion efficiency (PCE) of 3.7% is reported for OSC employing silver top electrodes, molybdenum trioxide (MoO3) as the hole-transport interlayer (HTL), active layer comprising of poly-3-hexylthiophene (P3HT) and [6,6]-phenyl C61 butyric acid methyl ester (PCBM) as well as a nanocrystalline solution-synthesized zinc oxide (ZnO) nanoparticle (NP) film as the electron-transport layer (ETL). By using solution-processable ZnO crystalline NPs as ETL, we can eliminate the typical high temperature processing/annealing step, which is widely adopted in the conventional ZnO ETL fabrication process via the sol-gel method. Such highly crystalline ZnO NP films can enhance charge collection at the electrodes. It is also found that inverted OSCs exhibit greater air stability and lifetime performance compared to the OSC employing the normal structure.

Biocompatible electrically conductive nanofibers from inorganic-organic shape memory polymers

A porous shape memory scaffold with both biomimetic structures and electrical conductivity properties is highly promising for nerve tissue engineering applications. In this study, a new shape memory polyurethane polymer which consists of inorganic polydimethylsiloxane (PDMS) segments with organic poly(ε-caprolactone) (PCL) segments was synthesized. Based on this poly(PCL/PDMS urethane), a series of electrically conductive nanofibers were electrospun by incorporating different amounts of carbon-black. Our results showed that after adding carbon black into nanofibers, the fiber diameters increased from 399±76 to 619±138nm, the crystallinity decreased from 33 to 25% and the resistivity reduced from 3.6 GΩ/mm to 1.8 kΩ/mm. Carbon black did not significantly influence the shape memory properties of the resulting nanofibers, and all the composite nanofibers exhibited decent shape recovery ratios of >90% and shape fixity ratios of >82% even after 5 thermo-mechanical cycles. PC12 cells were cultured on the shape memory nanofibers and the composite scaffolds showed good biocompatibility by promoting cell-cell interactions. Our study demonstrated that the poly(PCL/PDMS urethane)/carbon-black nanofibers with shape memory properties could be potentially used as smart 4-dimensional (4D) scaffolds for nerve tissue regeneration.

Imbalanced charge mobility in oxygen treated polythiophene/fullerene based bulk heterojunction solar cells

The effect of oxygen induced traps on charge mobility in bulk heterojunction solar cells using poly(3-hexylthiophene) (P3HT):l-(3-methoxycarbonyl)-propyl-l-phenyl-(6, 6) methanofullerene (PCBM) blend have been studied using photoinduced charge extraction by linearly increasing voltage (PhotoCELIV) technique. The solar cells exposed to oxygen exhibit dual PhotoCELIV peaks, whereas the solar cell without oxygen treatment show single PhotoCELIV peak with the charge mobility of the order of 10−4 cm2/V s. It is demonstrated that the oxygen treatment imbalance the charge mobility in the P3HT/PCBM photoactive layer, which affects the power conversion efficiency and lifetime of the solar cell. The single PhotoCELIV peak for the device without oxygen treatment indicates that the charge mobility is balanced, that causes the overlapping of electron and hole transients.

Unusual thermogelling behaviour of poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA)-based polymers polymerized in bulk

The bulk synthesis of (PDMAEMA)-based polymers and their unusual thermoreversible gelation in aqueous solutions are described. Herein we show the structure–property relationship between the sol-to-gel phase transition on the polymer characteristics and molecular weight. The tunable sensitivity of these supramolecular sol–gel reversible hydrogels are further described.

Recent Progress in Using Biomaterials as Vitreous Substitutes.

Vitreous substitutes are crucial adjuncts during vitreo-retinal surgery for retinal diseases such as complicated retinal detachment, macular holes, complications of diabetic retinopathy, and ocular trauma involving posterior segment. In retinal detachment surgery, an internal tamponade agent is required to provide internal pressure for reattachment of the detached neurosensory retina. Current available options serve only as a temporary surgical adduct or short-term solution and are associated with inherent problems. Despite many years of intensive research, an ideal vitreous substitute remains elusive. Indeed, the development of an ideal vitreous substitute requires the concerted efforts of synthetic chemists and biomaterial engineers, as well as ophthalmic surgeons. In this review, we propose that polymeric hydrogels present the future of artificial vitreous substitutes due to its high water composition, optical transparency, and rheological properties that closely mimic the natural vitreous. In particular, thermosensitive smart hydrogels, with reversible sol to gel change, have emerged as the material class with the most potential to succeed as ideal vitreous substitutes, facilitating easy implementation during surgery. Importantly, these smart hydrogels also display potential as efficacious drug delivery systems.

Biodegradable electronics: cornerstone for sustainable electronics and transient applications

Electronic devices have become ubiquitous in modern society and are prevalent in every facet of human activities. Although electronic devices have brought much convenience and value, the insatiable appetite for newer and more attractive devices has also created a growing ecological problem: managing electronic waste or e-waste. As the lifetime of electronic devices gets shorter and shorter, the pressure on e-waste management systems is mounting with no abate in sight. Therefore, an alternative to traditional electronics must be sought. Bio-degradable electronics have thus emerged as the most viable and ideal replacement to address the issue of uncontrollable e-waste. Bio-degradability will ensure that the waste generated will be at least non-toxic and even environmentally friendly. Furthermore, bio-degradable organic materials have also been shown to be biocompatible and human-friendly, being able to be metabolized safely in the body without causing adverse physiological reactions. As such, this developing class of “green” electronics is not only able to alleviate the growing e-waste problem, but also fulfils niche applications interfacing with the human body. This Review will introduce various bio-degradable organic materials that can serve as substitutes for the different components of an electronic device, highlight recent research achievements and applications in implementing such bio-degradable devices as well as present an overview of the printing technologies available that provide the low-cost and high throughput advantages of solution-processable organic materials over the traditional inorganic materials.

Biopolymer as an electron selective layer for inverted polymer solar cells

In this work, a solution-processable electron selective layer is introduced for inverted polymer solar cells (PSCs). Cationic biopolymer poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) is used as a solution-processable work function modifier of indium-tin-oxide transparent conducting electrode to yield efficient inverted PSCs of 3.3% under AM1.5G illumination, with poly(3-hexylthiophene) and [6,6]-phenyl-C61-butyric acid methyl ester as the active layer. Devices using PDMAEMA exhibit greater stability in ambient “working conditions” as compared to devices using ZnO, retaining 90% of peak power conversion efficiency after 8 weeks. Therefore, PDMAEMA has great potential as a universal work function modifier material with high robustness.

Enhanced Performance Using an SU-8 Dielectric Interlayer in a Bulk Heterojunction Organic Solar Cell

The effect of inserting an SU-8 dielectric interlayer into inverted bulk heterojunction (BHJ) organic solar cells (OSCs) was studied. Insertion of an ultrathin layer of SU-8 between the zinc oxide (ZnO) electron transport layer and the photoactive layer resulted in a smoother interface and a 14% enhancement in power conversion efficiency. The properties of devices with and without an SU-8 interlayer were investigated using transient photovoltage (TPV) and double injection (DoI) techniques, and it was found that devices with SU-8 show longer carrier lifetimes and greater mobility-lifetime (μ-τ) products than those without. Devices with SU-8 were also found to have improved stability. The results indicate that the insertion of an SU-8 interlayer reduces the recombination rate for photogenerated carriers without affecting the charge transport properties, improving overall performance and stability.